<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"><channel rdf:about="http://onlinelibrary.wiley.com/rss/journal/10.1111/(ISSN)1532-5415" xmlns="http://purl.org/rss/1.0/"><title>Journal of the American Geriatrics Society</title><description> Wiley Online Library : Journal of the American Geriatrics Society</description><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2F%28ISSN%291532-5415</link><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc</dc:publisher><dc:language xmlns:dc="http://purl.org/dc/elements/1.1/">en</dc:language><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/">© The American Geriatrics Society</dc:rights><prism:issn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">0002-8614</prism:issn><prism:eIssn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1532-5415</prism:eIssn><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-01T00:00:00-05:00</dc:date><prism:coverDisplayDate xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">July 2017</prism:coverDisplayDate><prism:volume xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">65</prism:volume><prism:number xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">7</prism:number><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1373</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1634</prism:endingPage><image rdf:resource="http://onlinelibrary.wiley.com/store/10.1111/jgs.2017.65.issue-7/asset/cover.gif?v=1&amp;s=9015d20cf66c8e2888099129bc249a815989a16d"/><items><rdf:Seq><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15014"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14997"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15012"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14960"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15011"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15016"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15017"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15008"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14990"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14968"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14965"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14986"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14952"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14999"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14994"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14977"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14984"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14949"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14962"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14995"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14996"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14934"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14971"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14992"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14954"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14988"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14989"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14904"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14991"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14983"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14927"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14961"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14957"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14938"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14917"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14980"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14955"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14982"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14973"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14924"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14942"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14958"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14985"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14972"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14970"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14944"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14964"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14956"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14976"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14950"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14978"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14979"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14974"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14935"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14959"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14937"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14911"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14948"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14913"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14936"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14625"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14627"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14941"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14842"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14881"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14916"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14852"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14887"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14891"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14795"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14794"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14804"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14811"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14813"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14818"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14819"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14812"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14823"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14810"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14816"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14826"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14827"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14834"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14829"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14837"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14838"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14844"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14932"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14943"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14832"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14846"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14840"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14865"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14879"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14870"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14815"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14875"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14828"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14890"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14939"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14886"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14945"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14864"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14850"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14866"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14885"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15006"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14626"/></rdf:Seq></items></channel><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15014" xmlns="http://purl.org/rss/1.0/"><title>Longitudinal Cognitive Profiles in Diabetes: Results From the National Alzheimer's Coordinating Center's Uniform Data</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15014</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Longitudinal Cognitive Profiles in Diabetes: Results From the National Alzheimer's Coordinating Center's Uniform Data</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mary Sano, Carolyn W. Zhu, Hillel Grossman, Corbett Schimming</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-08-03T08:40:32.989313-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.15014</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.15014</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15014</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs15014-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Background</h4><div class="para"><p>Diabetes is a risk factor for the development of cognitive impairment and possibly for accelerated progression to Alzheimer disease (AD) and other dementias, though the trajectory of cognitive decline in general and in specfic cognitive domains by diabetes is unclear.</p></div></div>
<div class="section" id="jgs15014-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Methods</h4><div class="para"><p>Using the National Alzheimer's Coordinating Center's Uniform Data Det (NACC-UDS) to identify cohorts of elders with normal cognition (N = 7,663) and mild cognitive impairment (MCI, N = 4,114), we compared overall cognitive composite and domain specific sub-scores and their progression over time between diabetic and non-diabetic subjects.</p></div></div>
<div class="section" id="jgs15014-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Diabetes was more common among those with MCI (14.7%) than among subjects who were cognitively normal (11.7%). In subjects who were cognitively normal, baseline cognitive composite scores, attention, and executive function sub-scores were lower in diabetics than non-diabetics (by 0.098, 0.066, and 0.015 points, respectively). Over time, cognitive composite score showed subtle worsening in non-diabetics (0.025 points every 6 months), with an additional worsening of 0.01 points every 6 months in diabetics compared to non-diabetics. In the MCI groups, baseline cognitive composite as well as attention and executive domain sub-scores were lower in diabetics than non-diabetics (by 0.078, 0.092, and 0.032 points, respectively). Over time, cognitive composite (by 0.103 points every 6 months) and all domain specific sub-scores showed subtle worsening in non-diabetics, but diabetics had significantly slower worsening than non-diabetics on both cognitive composite (by 0.028 points) and domain specific sub-scores.</p></div></div>
<div class="section" id="jgs15014-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Discussion</h4><div class="para"><p>Among elders, diabetes may be associated with lower cognitive performance, primarily in non-memory domains. However it is not associated with continued worsening, suggesting a static deficit with minimal memory involvement. This data suggest that diabetes may contribute more to a vascular profile of cognitive impairment than a profile more typical of AD.</p></div></div>
]]></content:encoded><description>

Background
Diabetes is a risk factor for the development of cognitive impairment and possibly for accelerated progression to Alzheimer disease (AD) and other dementias, though the trajectory of cognitive decline in general and in specfic cognitive domains by diabetes is unclear.


Methods
Using the National Alzheimer's Coordinating Center's Uniform Data Det (NACC-UDS) to identify cohorts of elders with normal cognition (N = 7,663) and mild cognitive impairment (MCI, N = 4,114), we compared overall cognitive composite and domain specific sub-scores and their progression over time between diabetic and non-diabetic subjects.


Results
Diabetes was more common among those with MCI (14.7%) than among subjects who were cognitively normal (11.7%). In subjects who were cognitively normal, baseline cognitive composite scores, attention, and executive function sub-scores were lower in diabetics than non-diabetics (by 0.098, 0.066, and 0.015 points, respectively). Over time, cognitive composite score showed subtle worsening in non-diabetics (0.025 points every 6 months), with an additional worsening of 0.01 points every 6 months in diabetics compared to non-diabetics. In the MCI groups, baseline cognitive composite as well as attention and executive domain sub-scores were lower in diabetics than non-diabetics (by 0.078, 0.092, and 0.032 points, respectively). Over time, cognitive composite (by 0.103 points every 6 months) and all domain specific sub-scores showed subtle worsening in non-diabetics, but diabetics had significantly slower worsening than non-diabetics on both cognitive composite (by 0.028 points) and domain specific sub-scores.


Discussion
Among elders, diabetes may be associated with lower cognitive performance, primarily in non-memory domains. However it is not associated with continued worsening, suggesting a static deficit with minimal memory involvement. This data suggest that diabetes may contribute more to a vascular profile of cognitive impairment than a profile more typical of AD.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14997" xmlns="http://purl.org/rss/1.0/"><title>Prevention of Alzheimer's Disease: Lessons Learned and Applied</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14997</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Prevention of Alzheimer's Disease: Lessons Learned and Applied</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">James E. Galvin</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-08-02T00:40:31.759919-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14997</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14997</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14997</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Special Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Alzheimer's disease (AD) affects more than 5 million Americans, with substantial consequences for individuals with AD, families, and society in terms of morbidity, mortality, and healthcare costs. With disease-modifying treatment trials unsuccessful at the present time and only medications to treat symptoms available, an emerging approach is prevention. Advances in diagnostic criteria, biomarker development, and greater understanding of the biophysiological basis of AD make these initiatives feasible. Ongoing pharmacological trials using anti-amyloid therapies are underway in sporadic and genetic forms of AD, although a large number of modifiable risk factors for AD have been identified in observational studies, many of which do not appear to exert effects through amyloid or tau. This suggests that prevention studies focusing on risk reduction and lifestyle modification may offer additional benefits. Rather than relying solely on large-sample, long-duration, randomized clinical trial designs, a precision medicine approach using N-of-1 trials may provide more-rapid information on whether personalized prevention plans can improve person-centered outcomes. Because there appear to be multiple pathways to developing AD, there may also be multiple ways to prevent or delay the onset of AD. Even if these precision approaches alone are not successful in preventing AD, they may greatly improve the likelihood of amyloid- or tau-specific therapies to reach their endpoints by reducing comorbidities. Keeping this in mind, dementia may be a disorder that develops over a lifetime, with individualized ways to build a better brain as we age.</p></div>
]]></content:encoded><description>
Alzheimer's disease (AD) affects more than 5 million Americans, with substantial consequences for individuals with AD, families, and society in terms of morbidity, mortality, and healthcare costs. With disease-modifying treatment trials unsuccessful at the present time and only medications to treat symptoms available, an emerging approach is prevention. Advances in diagnostic criteria, biomarker development, and greater understanding of the biophysiological basis of AD make these initiatives feasible. Ongoing pharmacological trials using anti-amyloid therapies are underway in sporadic and genetic forms of AD, although a large number of modifiable risk factors for AD have been identified in observational studies, many of which do not appear to exert effects through amyloid or tau. This suggests that prevention studies focusing on risk reduction and lifestyle modification may offer additional benefits. Rather than relying solely on large-sample, long-duration, randomized clinical trial designs, a precision medicine approach using N-of-1 trials may provide more-rapid information on whether personalized prevention plans can improve person-centered outcomes. Because there appear to be multiple pathways to developing AD, there may also be multiple ways to prevent or delay the onset of AD. Even if these precision approaches alone are not successful in preventing AD, they may greatly improve the likelihood of amyloid- or tau-specific therapies to reach their endpoints by reducing comorbidities. Keeping this in mind, dementia may be a disorder that develops over a lifetime, with individualized ways to build a better brain as we age.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15012" xmlns="http://purl.org/rss/1.0/"><title>A Systematic Review and Meta-Analysis of The Effect of Low Vitamin D on Cognition</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15012</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A Systematic Review and Meta-Analysis of The Effect of Low Vitamin D on Cognition</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Alicia M. Goodwill, Cassandra Szoeke</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-31T01:10:44.244684-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.15012</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.15012</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15012</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs15012-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Background/Objective</h4><div class="para"><p>With an aging population and no cure for dementia on the horizon, risk factor modification prior to disease onset is an urgent health priority. Therefore, this review examined the effect of low vitamin D status or vitamin D supplementation on cognition in midlife and older adults without a diagnosis of dementia.</p></div></div>
<div class="section" id="jgs15012-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Systematic review and random effect meta-analysis.</p></div></div>
<div class="section" id="jgs15012-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Observational (cross-sectional and longitudinal cohort) studies comparing low and high vitamin D status and interventions comparing vitamin D supplementation with a control group were included in the review and meta-analysis.</p></div></div>
<div class="section" id="jgs15012-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Studies including adults and older adults without a dementia diagnosis were included.</p></div></div>
<div class="section" id="jgs15012-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Medline (PubMed), AMED, Psych INFO, and Cochrane Central databases were searched for articles until August 2016. The Newcastle-Ottawa Scale and Physiotherapy Evidence Database assessed methodological quality of all studies.</p></div></div>
<div class="section" id="jgs15012-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Twenty-six observational and three intervention studies (n = 19–9,556) were included in the meta-analysis. Low vitamin D was associated with worse cognitive performance (OR = 1.24, CI = 1.14–1.35) and cognitive decline (OR = 1.26, CI = 1.09–1.23); with cross-sectional yielding a stronger effect compared to longitudinal studies. Vitamin D supplementation showed no significant benefit on cognition compared with control (SMD = 0.21, CI = −0.05 to 0.46).</p></div></div>
<div class="section" id="jgs15012-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Observational evidence demonstrates low vitamin D is related to poorer cognition; however, interventional studies are yet to show a clear benefit from vitamin D supplementation. From the evidence to date, there is likely a therapeutic age window relevant to the development of disease and therefore vitamin D therapy. Longitudinal lifespan studies are necessary to depict the optimal timing and duration in which repletion of vitamin D may protect against cognitive decline and dementia in aging, to better inform trials and practice towards a successful therapy.</p></div></div>
]]></content:encoded><description>

Background/Objective
With an aging population and no cure for dementia on the horizon, risk factor modification prior to disease onset is an urgent health priority. Therefore, this review examined the effect of low vitamin D status or vitamin D supplementation on cognition in midlife and older adults without a diagnosis of dementia.


Design
Systematic review and random effect meta-analysis.


Setting
Observational (cross-sectional and longitudinal cohort) studies comparing low and high vitamin D status and interventions comparing vitamin D supplementation with a control group were included in the review and meta-analysis.


Participants
Studies including adults and older adults without a dementia diagnosis were included.


Measurements
Medline (PubMed), AMED, Psych INFO, and Cochrane Central databases were searched for articles until August 2016. The Newcastle-Ottawa Scale and Physiotherapy Evidence Database assessed methodological quality of all studies.


Results
Twenty-six observational and three intervention studies (n = 19–9,556) were included in the meta-analysis. Low vitamin D was associated with worse cognitive performance (OR = 1.24, CI = 1.14–1.35) and cognitive decline (OR = 1.26, CI = 1.09–1.23); with cross-sectional yielding a stronger effect compared to longitudinal studies. Vitamin D supplementation showed no significant benefit on cognition compared with control (SMD = 0.21, CI = −0.05 to 0.46).


Conclusion
Observational evidence demonstrates low vitamin D is related to poorer cognition; however, interventional studies are yet to show a clear benefit from vitamin D supplementation. From the evidence to date, there is likely a therapeutic age window relevant to the development of disease and therefore vitamin D therapy. Longitudinal lifespan studies are necessary to depict the optimal timing and duration in which repletion of vitamin D may protect against cognitive decline and dementia in aging, to better inform trials and practice towards a successful therapy.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14960" xmlns="http://purl.org/rss/1.0/"><title>Accelerometer-Measured Moderate to Vigorous Physical Activity and Incidence Rates of Falls in Older Women</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14960</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Accelerometer-Measured Moderate to Vigorous Physical Activity and Incidence Rates of Falls in Older Women</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">David M. Buchner, Eileen Rillamas-Sun, Chongzhi Di, Michael J. LaMonte, Stephen W. Marshall, Julie Hunt, Yuzheng Zhang, Dori E. Rosenberg, I-Min Lee, Kelly R. Evenson, Amy H. Herring, Cora E. Lewis, Marcia L. Stefanick, Andrea Z. LaCroix</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-29T00:05:27.821877-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14960</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14960</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14960</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14960-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To examine whether moderate to vigorous physical activity (MVPA) measured using accelerometry is associated with incident falls and whether associations differ according to physical function or history of falls.</p></div></div>
<div class="section" id="jgs14960-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Prospective study with baseline data collection from 2012 to 2014 and 1 year of follow-up.</p></div></div>
<div class="section" id="jgs14960-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Women's Health Initiative participants living in the United States.</p></div></div>
<div class="section" id="jgs14960-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Ambulatory women aged 63 to 99 (N = 5,545).</p></div></div>
<div class="section" id="jgs14960-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Minutes of MVPA per day measured using an accelerometer, functional status measured using the Short Physical Performance Battery (SPPB), fall risk factors assessed using a questionnaire, fall injuries assessed in a telephone interview, incident falls ascertained from fall calendars.</p></div></div>
<div class="section" id="jgs14960-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Incident rate ratios (IRRs) revealed greater fall risk in women in the lowest quartile of MVPA compared to those in the highest (IRR = 1.18, 95% confidence interval = 1.01–1.38), adjusted for age, race and ethnicity, and fall risk factors. Fall rates were not significantly associated with MVPA in women with high SPPB scores (9–12) or one or fewer falls in the previous year, but in women with low SPPB scores (≤ 8) or a history of frequent falls, fall rates were higher in women with lower MVPA levels than in those with higher levels (interaction <em>P</em> &lt; .03 and &lt; .001, respectively). Falls in women with MVPA above the median were less likely to involve injuries requiring medical treatment (9.9%) than falls in women with lower MVPA levels (13.0%) (<em>P</em> &lt; .001).</p></div></div>
<div class="section" id="jgs14960-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>These findings indicate that falls are not more common or injurious in older women who engage in higher levels of MVPA. These findings support encouraging women to engage in the amounts and types of MVPA that they prefer. Older women with low physical function or frequent falls with low levels of MVPA are a high-risk group for whom vigilance about falls prevention is warranted.</p></div></div>
]]></content:encoded><description>

Objectives
To examine whether moderate to vigorous physical activity (MVPA) measured using accelerometry is associated with incident falls and whether associations differ according to physical function or history of falls.


Design
Prospective study with baseline data collection from 2012 to 2014 and 1 year of follow-up.


Setting
Women's Health Initiative participants living in the United States.


Participants
Ambulatory women aged 63 to 99 (N = 5,545).


Measurements
Minutes of MVPA per day measured using an accelerometer, functional status measured using the Short Physical Performance Battery (SPPB), fall risk factors assessed using a questionnaire, fall injuries assessed in a telephone interview, incident falls ascertained from fall calendars.


Results
Incident rate ratios (IRRs) revealed greater fall risk in women in the lowest quartile of MVPA compared to those in the highest (IRR = 1.18, 95% confidence interval = 1.01–1.38), adjusted for age, race and ethnicity, and fall risk factors. Fall rates were not significantly associated with MVPA in women with high SPPB scores (9–12) or one or fewer falls in the previous year, but in women with low SPPB scores (≤ 8) or a history of frequent falls, fall rates were higher in women with lower MVPA levels than in those with higher levels (interaction P &lt; .03 and &lt; .001, respectively). Falls in women with MVPA above the median were less likely to involve injuries requiring medical treatment (9.9%) than falls in women with lower MVPA levels (13.0%) (P &lt; .001).


Conclusion
These findings indicate that falls are not more common or injurious in older women who engage in higher levels of MVPA. These findings support encouraging women to engage in the amounts and types of MVPA that they prefer. Older women with low physical function or frequent falls with low levels of MVPA are a high-risk group for whom vigilance about falls prevention is warranted.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15011" xmlns="http://purl.org/rss/1.0/"><title>Disparities in Treatment of Older Adults with Suicide Risk in the Emergency Department</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15011</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Disparities in Treatment of Older Adults with Suicide Risk in the Emergency Department</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sarah A. Arias, Edwin D. Boudreaux, Daniel L. Segal, Ivan Miller, Carlos A. Camargo, Marian E. Betz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-28T00:35:36.018411-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.15011</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.15011</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15011</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Brief Report</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs15011-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Background/Objective</h4><div class="para"><p>We described characteristics and treatment received for older (≥60 years) vs younger (&lt;60 years) adult emergency department (ED) patients with suicide risk.</p></div></div>
<div class="section" id="jgs15011-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Retrospective chart review.</p></div></div>
<div class="section" id="jgs15011-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>An ED with universal screening for suicide risk.</p></div></div>
<div class="section" id="jgs15011-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Eligible charts included a random sample of adults (≥18 years) who screened positive for suicidal ideation (SI) in past 2 weeks and/or a suicide attempt (SA) within the past 6 months. Visit dates were from May 2014 to September 2016.</p></div></div>
<div class="section" id="jgs15011-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>A total of 800 charts were reviewed, with oversampling of older adults. Of the 200 older adults sampled, fewer older adults compared to younger adults (n = 600) had a chief complaint involving psychiatric behavior (53% vs 70%) or self-harm behavior (26% vs 36%). Although a higher number of older adults (93%) had documentation of current SI compared to younger adults (79%), fewer older adults (17%) reported SA in the past 2 weeks compared to younger adults (23%). Of those with a positive suicide screen who were discharged home, less than half of older adults received a mental health evaluation during their visit (42%, 95% CI 34–52) compared to 66% (95% CI 61–70) of younger adults who met the same criteria. Similarly, fewer older, than younger, adult patients with current SI/SA received referral resources (34%; 95% CI 26–43; vs 60%; 95% CI 55–65).</p></div></div>
<div class="section" id="jgs15011-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Significantly fewer suicidal older adult patients who were discharged home received a mental health evaluation when compared to similar younger adults. These findings highlight an important area for improvement in the treatment of older adults at risk for suicide.</p></div></div>
]]></content:encoded><description>

Background/Objective
We described characteristics and treatment received for older (≥60 years) vs younger (&lt;60 years) adult emergency department (ED) patients with suicide risk.


Design
Retrospective chart review.


Setting
An ED with universal screening for suicide risk.


Participants
Eligible charts included a random sample of adults (≥18 years) who screened positive for suicidal ideation (SI) in past 2 weeks and/or a suicide attempt (SA) within the past 6 months. Visit dates were from May 2014 to September 2016.


Results
A total of 800 charts were reviewed, with oversampling of older adults. Of the 200 older adults sampled, fewer older adults compared to younger adults (n = 600) had a chief complaint involving psychiatric behavior (53% vs 70%) or self-harm behavior (26% vs 36%). Although a higher number of older adults (93%) had documentation of current SI compared to younger adults (79%), fewer older adults (17%) reported SA in the past 2 weeks compared to younger adults (23%). Of those with a positive suicide screen who were discharged home, less than half of older adults received a mental health evaluation during their visit (42%, 95% CI 34–52) compared to 66% (95% CI 61–70) of younger adults who met the same criteria. Similarly, fewer older, than younger, adult patients with current SI/SA received referral resources (34%; 95% CI 26–43; vs 60%; 95% CI 55–65).


Conclusions
Significantly fewer suicidal older adult patients who were discharged home received a mental health evaluation when compared to similar younger adults. These findings highlight an important area for improvement in the treatment of older adults at risk for suicide.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15016" xmlns="http://purl.org/rss/1.0/"><title>Frailty and Potentially Inappropriate Medication Use at Nursing Home Transition</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15016</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Frailty and Potentially Inappropriate Medication Use at Nursing Home Transition</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Laura C. Maclagan, Colleen J. Maxwell, Sima Gandhi, Jun Guan, Chaim M. Bell, David B. Hogan, Nick Daneman, Sudeep S. Gill, Andrew M. Morris, Lianne Jeffs, Michael A. Campitelli, Dallas P. Seitz, Susan E. Bronskill</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-28T00:35:27.192088-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.15016</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.15016</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15016</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs15016-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Background/Objectives</h4><div class="para"><p>To estimate the prevalence of potentially inappropriate medication (PIM) use among older adults with cognitive impairment or dementia prior to and following admission to nursing homes and in relation to frailty.</p></div></div>
<div class="section" id="jgs15016-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Retrospective cohort study using health administrative databases.</p></div></div>
<div class="section" id="jgs15016-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Ontario, Canada.</p></div></div>
<div class="section" id="jgs15016-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>41,351 individuals with cognitive impairment or dementia, aged 66+ years newly admitted to nursing home between 2011 and 2014.</p></div></div>
<div class="section" id="jgs15016-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>PIMs were defined with 2015 Beers Criteria and included antipsychotics, H<sub>2</sub>-receptor antagonists, benzodiazepines, and drugs with strong anticholinergic properties. Medication information was obtained at nursing home admission and in the subsequent 180 days. Multivariable Cox proportional-hazards models were used to assess the impact of frailty status (determined by a 72-item frailty index) on the hazard of starting and discontinuing PIMs.</p></div></div>
<div class="section" id="jgs15016-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>At admission, 44% of residents with cognitive impairment or dementia were on a PIM and prevalence varied by frailty (38.7% non-frail, 42.8% pre-frail, and 48.1% frail, <em>P</em> &lt; .001). Following admission, many residents discontinued PIMs (23.5% for antipsychotics, 49.3% benzodiazepines, 32.2% anticholinergics, and 30.9% H<sub>2</sub>-receptor antagonists). However, PIMs were also introduced with 10.9% newly started on antipsychotics, benzodiazepines (10.1%), anticholinergics (6.6%), and H<sub>2</sub>-receptor antagonists (1.2%). After adjustment for other characteristics, frail residents had a similar risk of PIM discontinuation as non-frail residents except for anticholinergics (HR = 1.21, 95% CI 1.06–1.39) but were more likely to be newly prescribed benzodiazepines (HR = 1.32, 95% CI 1.20–1.44), antipsychotics (HR = 1.36, 1.23–1.49), and anticholinergics (HR = 1.34, 95% CI 1.20–1.50).</p></div></div>
<div class="section" id="jgs15016-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Many residents with cognitive impairment or dementia enter nursing homes on PIMs. PIMs are more likely to be started in frail individuals following admission. Interventions to support deprescribing of PIMs should be implemented targeting frail individuals during the transition to nursing home.</p></div></div>
]]></content:encoded><description>

Background/Objectives
To estimate the prevalence of potentially inappropriate medication (PIM) use among older adults with cognitive impairment or dementia prior to and following admission to nursing homes and in relation to frailty.


Design
Retrospective cohort study using health administrative databases.


Setting
Ontario, Canada.


Participants
41,351 individuals with cognitive impairment or dementia, aged 66+ years newly admitted to nursing home between 2011 and 2014.


Measurements
PIMs were defined with 2015 Beers Criteria and included antipsychotics, H2-receptor antagonists, benzodiazepines, and drugs with strong anticholinergic properties. Medication information was obtained at nursing home admission and in the subsequent 180 days. Multivariable Cox proportional-hazards models were used to assess the impact of frailty status (determined by a 72-item frailty index) on the hazard of starting and discontinuing PIMs.


Results
At admission, 44% of residents with cognitive impairment or dementia were on a PIM and prevalence varied by frailty (38.7% non-frail, 42.8% pre-frail, and 48.1% frail, P &lt; .001). Following admission, many residents discontinued PIMs (23.5% for antipsychotics, 49.3% benzodiazepines, 32.2% anticholinergics, and 30.9% H2-receptor antagonists). However, PIMs were also introduced with 10.9% newly started on antipsychotics, benzodiazepines (10.1%), anticholinergics (6.6%), and H2-receptor antagonists (1.2%). After adjustment for other characteristics, frail residents had a similar risk of PIM discontinuation as non-frail residents except for anticholinergics (HR = 1.21, 95% CI 1.06–1.39) but were more likely to be newly prescribed benzodiazepines (HR = 1.32, 95% CI 1.20–1.44), antipsychotics (HR = 1.36, 1.23–1.49), and anticholinergics (HR = 1.34, 95% CI 1.20–1.50).


Conclusion
Many residents with cognitive impairment or dementia enter nursing homes on PIMs. PIMs are more likely to be started in frail individuals following admission. Interventions to support deprescribing of PIMs should be implemented targeting frail individuals during the transition to nursing home.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15017" xmlns="http://purl.org/rss/1.0/"><title>Poor Appetite and Dietary Intake in Community-Dwelling Older Adults</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15017</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Poor Appetite and Dietary Intake in Community-Dwelling Older Adults</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Barbara S. Meij, Hanneke A. H. Wijnhoven, Jung S. Lee, Denise K. Houston, Trisha Hue, Tamara B. Harris, Stephen B. Kritchevsky, Anne B. Newman, Marjolein Visser</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-26T02:05:19.923508-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.15017</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.15017</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15017</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs15017-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Background/objectives</h4><div class="para"><p>Poor appetite in older adults leads to sub-optimal food intake and increases the risk of undernutrition. The impact of poor appetite on food intake in older adults is unknown. The aim of this study was to examine the differences in food intake among older community-dwelling adults with different reported appetite levels.</p></div></div>
<div class="section" id="jgs15017-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Cross-sectional analysis of data from a longitudinal prospective study.</p></div></div>
<div class="section" id="jgs15017-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Health, aging, and body composition study performed in the USA.</p></div></div>
<div class="section" id="jgs15017-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>2,597 community-dwelling adults aged 70–79.</p></div></div>
<div class="section" id="jgs15017-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>A semi-quantitative, interviewer-administered, 108-item food frequency questionnaire designed to estimate dietary intake. Poor appetite was defined as the report of a moderate, poor, or very poor appetite in the past month and was compared with good or very good appetite.</p></div></div>
<div class="section" id="jgs15017-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The mean age of the study sample was 74.5 ± 2.8 years; 48.2% were men, 37.7% were black, and 21.8% reported a poor appetite. After adjustment for total energy intake and potential confounders (including biting/chewing problems), participants with a poor appetite had a significantly lower consumption of protein and dietary fiber, solid foods, protein rich foods, whole grains, fruits, and vegetables, but a higher consumption of dairy foods, fats, oils, sweets, and sodas compared to participants with very good appetite. In addition, they were less likely to report consumption of significant larger portion sizes.</p></div></div>
<div class="section" id="jgs15017-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Older adults reporting a poor appetite showed a different dietary intake pattern compared to those with (very) good appetite. Better understanding of the specific dietary intake pattern related to a poor appetite in older adults can be used for nutrition interventions to enhance food intake, diet variety, and diet quality.</p></div></div>
]]></content:encoded><description>

Background/objectives
Poor appetite in older adults leads to sub-optimal food intake and increases the risk of undernutrition. The impact of poor appetite on food intake in older adults is unknown. The aim of this study was to examine the differences in food intake among older community-dwelling adults with different reported appetite levels.


Design
Cross-sectional analysis of data from a longitudinal prospective study.


Setting
Health, aging, and body composition study performed in the USA.


Participants
2,597 community-dwelling adults aged 70–79.


Measurements
A semi-quantitative, interviewer-administered, 108-item food frequency questionnaire designed to estimate dietary intake. Poor appetite was defined as the report of a moderate, poor, or very poor appetite in the past month and was compared with good or very good appetite.


Results
The mean age of the study sample was 74.5 ± 2.8 years; 48.2% were men, 37.7% were black, and 21.8% reported a poor appetite. After adjustment for total energy intake and potential confounders (including biting/chewing problems), participants with a poor appetite had a significantly lower consumption of protein and dietary fiber, solid foods, protein rich foods, whole grains, fruits, and vegetables, but a higher consumption of dairy foods, fats, oils, sweets, and sodas compared to participants with very good appetite. In addition, they were less likely to report consumption of significant larger portion sizes.


Conclusion
Older adults reporting a poor appetite showed a different dietary intake pattern compared to those with (very) good appetite. Better understanding of the specific dietary intake pattern related to a poor appetite in older adults can be used for nutrition interventions to enhance food intake, diet variety, and diet quality.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15008" xmlns="http://purl.org/rss/1.0/"><title>Tai Chi for Risk of Falls. A Meta-analysis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15008</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Tai Chi for Risk of Falls. A Meta-analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rafael Lomas-Vega, Esteban Obrero-Gaitán, Francisco J. Molina-Ortega, Rafael Del-Pino-Casado</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-24T00:01:03.03493-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.15008</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.15008</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15008</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs15008-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To analyze the effectiveness of tai chi for falls prevention.</p></div></div>
<div class="section" id="jgs15008-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Systematic review and meta-analysis.</p></div></div>
<div class="section" id="jgs15008-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Pubmed, Scopus, CINHAL, and Physiotherapy Evidence Database (PEDro) were searched to May 26, 2016.</p></div></div>
<div class="section" id="jgs15008-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Older adult population and at-risk adults.</p></div></div>
<div class="section" id="jgs15008-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Intervention</h4><div class="para"><p>Randomized controlled trials analyzing the effect of tai chi versus other treatments on risk of falls.</p></div></div>
<div class="section" id="jgs15008-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>The incidence rate ratio (IRR) for falls incidence and hazard ratio (HR) for time to first fall.</p></div></div>
<div class="section" id="jgs15008-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The search strategy identified 891 potentially eligible studies, of which 10 met the inclusion criteria. There was high-quality evidence of a medium protective effect for fall incidence over the short term (IRR = 0.57; 95% CI = 0.46, 0.70) and a small protective effect over the long term (IRR = 0.87; 95% CI = 0.77, 0.98). Regarding injurious falls, we found very low-quality evidence of a medium protective effect over the short term (IRR = 0.50; 95% CI = 0.33, 0.74) and a small effect over the long term (IRR = 0.72; 95% CI = 0.54, 0.95). There was no effect on time to first fall, with moderate quality of evidence (HR = 0.98; 95% CI = 0.69, 1.37).</p></div></div>
<div class="section" id="jgs15008-sec-0008" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>In at-risk adults and older adults, tai chi practice may reduce the rate of falls and injury-related falls over the short term (&lt;12 months) by approximately 43% and 50%, respectively. Tai chi practice may not influence time to first fall in these populations. Due to the low quality of evidence, more studies investigating the effects of tai chi on injurious falls and time to first fall are required.</p></div></div>
]]></content:encoded><description>

Objectives
To analyze the effectiveness of tai chi for falls prevention.


Design
Systematic review and meta-analysis.


Setting
Pubmed, Scopus, CINHAL, and Physiotherapy Evidence Database (PEDro) were searched to May 26, 2016.


Participants
Older adult population and at-risk adults.


Intervention
Randomized controlled trials analyzing the effect of tai chi versus other treatments on risk of falls.


Measurements
The incidence rate ratio (IRR) for falls incidence and hazard ratio (HR) for time to first fall.


Results
The search strategy identified 891 potentially eligible studies, of which 10 met the inclusion criteria. There was high-quality evidence of a medium protective effect for fall incidence over the short term (IRR = 0.57; 95% CI = 0.46, 0.70) and a small protective effect over the long term (IRR = 0.87; 95% CI = 0.77, 0.98). Regarding injurious falls, we found very low-quality evidence of a medium protective effect over the short term (IRR = 0.50; 95% CI = 0.33, 0.74) and a small effect over the long term (IRR = 0.72; 95% CI = 0.54, 0.95). There was no effect on time to first fall, with moderate quality of evidence (HR = 0.98; 95% CI = 0.69, 1.37).


Conclusion
In at-risk adults and older adults, tai chi practice may reduce the rate of falls and injury-related falls over the short term (&lt;12 months) by approximately 43% and 50%, respectively. Tai chi practice may not influence time to first fall in these populations. Due to the low quality of evidence, more studies investigating the effects of tai chi on injurious falls and time to first fall are required.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14990" xmlns="http://purl.org/rss/1.0/"><title>Effectiveness of Light Therapy in Cognitively Impaired Persons: A Metaanalysis of Randomized Controlled Trials</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14990</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effectiveness of Light Therapy in Cognitively Impaired Persons: A Metaanalysis of Randomized Controlled Trials</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Huei-Ling Chiu, Pi-Tuan Chan, Hsin Chu, Shu-Tai Sheen Hsiao, Doresses Liu, Chueh-Ho Lin, Kuei-Ru Chou</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-22T04:10:43.965734-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14990</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14990</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14990</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14990-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To explore the effects of light therapy on behavioral disturbances (BDs), sleep quality, and depression.</p></div></div>
<div class="section" id="jgs14990-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Meta-analysis of randomized controlled trials.</p></div></div>
<div class="section" id="jgs14990-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>PubMed, Cochrane Library, Medline, EMBASE, Web of Science, and clinicaltrials.gov of selected randomized controlled trials and previous systematic reviews were searched.</p></div></div>
<div class="section" id="jgs14990-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Cognitively impaired persons.</p></div></div>
<div class="section" id="jgs14990-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Information was extracted on study characteristics, quality assessment, and outcomes. Outcome measures included BDs, sleep quality, and depression.</p></div></div>
<div class="section" id="jgs14990-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Nine randomized controlled trials were examined. The results showed that light therapy has a moderate effect on BD (g = −0.61) and depression (g = −0.58) and a small effect on total sleep time at night (g = 0.25). Subgroup analysis indicated that a light intensity of 2,500 lux or greater has a greater effect on depression than an intensity of less than 2,500 lux (P = .03), and the low risk of bias in blinding was superior to the RCTs deemed to be of high or unclear risk of bias in blinding in terms of BD (P = .02).</p></div></div>
<div class="section" id="jgs14990-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Light therapy can relieve BD, improve sleep quality, and alleviate symptoms of depression for cognitively impaired persons.</p></div></div>
]]></content:encoded><description>

Objectives
To explore the effects of light therapy on behavioral disturbances (BDs), sleep quality, and depression.


Design
Meta-analysis of randomized controlled trials.


Setting
PubMed, Cochrane Library, Medline, EMBASE, Web of Science, and clinicaltrials.gov of selected randomized controlled trials and previous systematic reviews were searched.


Participants
Cognitively impaired persons.


Measurements
Information was extracted on study characteristics, quality assessment, and outcomes. Outcome measures included BDs, sleep quality, and depression.


Results
Nine randomized controlled trials were examined. The results showed that light therapy has a moderate effect on BD (g = −0.61) and depression (g = −0.58) and a small effect on total sleep time at night (g = 0.25). Subgroup analysis indicated that a light intensity of 2,500 lux or greater has a greater effect on depression than an intensity of less than 2,500 lux (P = .03), and the low risk of bias in blinding was superior to the RCTs deemed to be of high or unclear risk of bias in blinding in terms of BD (P = .02).


Conclusion
Light therapy can relieve BD, improve sleep quality, and alleviate symptoms of depression for cognitively impaired persons.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14968" xmlns="http://purl.org/rss/1.0/"><title>Effect of a Community-Based Service Learning Experience in Geriatrics on Internal Medicine Residents and Community Participants</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14968</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effect of a Community-Based Service Learning Experience in Geriatrics on Internal Medicine Residents and Community Participants</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rachel K. Miller, Jennifer Michener, Phyllis Yang, Karen Goldstein, Jennine Groce-Martin, Gala True, Jerry Johnson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-22T04:10:37.832099-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14968</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14968</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14968</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Education and Training</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Community-based service learning (CBSL) provides an opportunity to teach internal medicine residents the social context of aging and clinical concepts. The objectives of the current study were to demonstrate the feasibility of a CBSL program targeting internal medicine residents and to assess its effect on medical residents and community participants. internal medicine residents participated in a CBSL experience for half a day during ambulatory blocks from 2011 to 2014. Residents attended a senior housing unit or center, delivered a presentation about a geriatric health topic, toured the facility, and received information about local older adult resources. Residents evaluated the experience. Postgraduate Year 3 internal medicine residents (n = 71) delivered 64 sessions. Residents felt that the experience increased their ability to communicate effectively with older adults (mean 3.91 ± 0.73 on a Likert scale with 5 = strongly agree), increased their knowledge of resources (4.09 ± 1.01), expanded their knowledge of a health topic pertinent to aging (3.48 ± 1.09), and contributed to their capacity to evaluate and care for older adults (3.84 ± 0.67). Free-text responses demonstrated that residents thought that this program would change their practice. Of 815 older adults surveyed from 36 discrete teaching sessions, 461 (56%) thought that the medical residents delivered health information clearly (4.55 ± 0.88) and that the health topics were relevant (4.26 ± 0.92). Free-text responses showed that the program helped them understand their health concerns. This CBSL program is a feasible and effective tool for teaching internal medicine residents and older adults.</p></div>
]]></content:encoded><description>
Community-based service learning (CBSL) provides an opportunity to teach internal medicine residents the social context of aging and clinical concepts. The objectives of the current study were to demonstrate the feasibility of a CBSL program targeting internal medicine residents and to assess its effect on medical residents and community participants. internal medicine residents participated in a CBSL experience for half a day during ambulatory blocks from 2011 to 2014. Residents attended a senior housing unit or center, delivered a presentation about a geriatric health topic, toured the facility, and received information about local older adult resources. Residents evaluated the experience. Postgraduate Year 3 internal medicine residents (n = 71) delivered 64 sessions. Residents felt that the experience increased their ability to communicate effectively with older adults (mean 3.91 ± 0.73 on a Likert scale with 5 = strongly agree), increased their knowledge of resources (4.09 ± 1.01), expanded their knowledge of a health topic pertinent to aging (3.48 ± 1.09), and contributed to their capacity to evaluate and care for older adults (3.84 ± 0.67). Free-text responses demonstrated that residents thought that this program would change their practice. Of 815 older adults surveyed from 36 discrete teaching sessions, 461 (56%) thought that the medical residents delivered health information clearly (4.55 ± 0.88) and that the health topics were relevant (4.26 ± 0.92). Free-text responses showed that the program helped them understand their health concerns. This CBSL program is a feasible and effective tool for teaching internal medicine residents and older adults.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14965" xmlns="http://purl.org/rss/1.0/"><title>ENabling Reduction of Low-grade Inflammation in SEniors Pilot Study: Concept, Rationale, and Design</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14965</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">ENabling Reduction of Low-grade Inflammation in SEniors Pilot Study: Concept, Rationale, and Design</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Todd M. Manini, Stephen D. Anton, Daniel P. Beavers, Jane A. Cauley, Mark A. Espeland, Roger A. Fielding, Stephen B. Kritchevsky, Christiaan Leeuwenburgh, Kristina H. Lewis, Christine Liu, Mary M. McDermott, Michael E. Miller, Russell P. Tracy, Jeremy D. Walston, Barbara Radziszewska, Jane Lu, Cindy Stowe, Samuel Wu, Anne B. Newman, Walter T. Ambrosius, Marco Pahor, </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-22T04:10:30.599746-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14965</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14965</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14965</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14965-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To test two interventions to reduce interleukin (IL)-6 levels, an indicator of low-grade chronic inflammation and an independent risk factor for impaired mobility and slow walking speed in older adults.</p></div></div>
<div class="section" id="jgs14965-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>The ENabling Reduction of low-Grade Inflammation in SEniors (ENRGISE) Pilot Study was a multicenter, double-blind, placebo-controlled randomized pilot trial of two interventions to reduce IL-6 levels.</p></div></div>
<div class="section" id="jgs14965-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Five university-based research centers.</p></div></div>
<div class="section" id="jgs14965-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Target enrollment was 300 men and women aged 70 and older with an average plasma IL-6 level between 2.5 and 30 pg/mL measured twice at least 1 week apart. Participants had low to moderate physical function, defined as self-reported difficulty walking one-quarter of a mile or climbing a flight of stairs and usual walk speed of less than 1 m/s on a 4-m usual-pace walk.</p></div></div>
<div class="section" id="jgs14965-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Intervention</h4><div class="para"><p>Participants were randomized to losartan, omega-3 fish oil (<em>ω</em>-3), combined losartan and <em>ω</em>-3, or placebo. Randomization was stratified depending on eligibility for each group. A titration schedule was implemented to reach a dose that was safe and effective for IL-6 reduction. Maximal doses were 100 mg/d for losartan and 2.8 g/d for <em>ω</em>-3.</p></div></div>
<div class="section" id="jgs14965-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>IL-6, walking speed over 400 m, physical function (Short Physical Performance Battery), other inflammatory markers, safety, tolerability, frailty domains, and maximal leg strength were measured.</p></div></div>
<div class="section" id="jgs14965-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Results from the ENRGISE Pilot Study will provide recruitment yields, feasibility, medication tolerance and adherence, and preliminary data to help justify a sample size for a more definitive randomized trial.</p></div></div>
<div class="section" id="jgs14965-sec-0008" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>The ENRGISE Pilot Study will inform a larger subsequent trial that is expected to have important clinical and public health implications for the growing population of older adults with low-grade chronic inflammation and mobility limitations.</p></div></div>
]]></content:encoded><description>

Objectives
To test two interventions to reduce interleukin (IL)-6 levels, an indicator of low-grade chronic inflammation and an independent risk factor for impaired mobility and slow walking speed in older adults.


Design
The ENabling Reduction of low-Grade Inflammation in SEniors (ENRGISE) Pilot Study was a multicenter, double-blind, placebo-controlled randomized pilot trial of two interventions to reduce IL-6 levels.


Setting
Five university-based research centers.


Participants
Target enrollment was 300 men and women aged 70 and older with an average plasma IL-6 level between 2.5 and 30 pg/mL measured twice at least 1 week apart. Participants had low to moderate physical function, defined as self-reported difficulty walking one-quarter of a mile or climbing a flight of stairs and usual walk speed of less than 1 m/s on a 4-m usual-pace walk.


Intervention
Participants were randomized to losartan, omega-3 fish oil (ω-3), combined losartan and ω-3, or placebo. Randomization was stratified depending on eligibility for each group. A titration schedule was implemented to reach a dose that was safe and effective for IL-6 reduction. Maximal doses were 100 mg/d for losartan and 2.8 g/d for ω-3.


Measurements
IL-6, walking speed over 400 m, physical function (Short Physical Performance Battery), other inflammatory markers, safety, tolerability, frailty domains, and maximal leg strength were measured.


Results
Results from the ENRGISE Pilot Study will provide recruitment yields, feasibility, medication tolerance and adherence, and preliminary data to help justify a sample size for a more definitive randomized trial.


Conclusion
The ENRGISE Pilot Study will inform a larger subsequent trial that is expected to have important clinical and public health implications for the growing population of older adults with low-grade chronic inflammation and mobility limitations.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14986" xmlns="http://purl.org/rss/1.0/"><title>Hearing Impairment and Incident Dementia: Findings from the English Longitudinal Study of Ageing</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14986</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Hearing Impairment and Incident Dementia: Findings from the English Longitudinal Study of Ageing</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hilary R. Davies, Dorina Cadar, Annie Herbert, Martin Orrell, Andrew Steptoe</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-22T04:10:23.390967-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14986</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14986</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14986</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Management of the Older Adult</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14986-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To determine whether hearing loss is associated with incident physician-diagnosed dementia in a representative sample.</p></div></div>
<div class="section" id="jgs14986-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Retrospective cohort study.</p></div></div>
<div class="section" id="jgs14986-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>English Longitudinal Study of Ageing.</p></div></div>
<div class="section" id="jgs14986-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Adults aged 50 and older.</p></div></div>
<div class="section" id="jgs14986-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Cross-sectional associations between self-reported (n = 7,865) and objective hearing measures (n = 6,902) and dementia were examined using multinomial-logistic regression. The longitudinal association between self-reported hearing at Wave 2 (2004/05) and cumulative physician-diagnosed dementia up to Wave 7 (2014/15) was modelled using Cox proportional hazards regression.</p></div></div>
<div class="section" id="jgs14986-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>After adjustment for potential confounders, in cross-sectional analysis, participants who had self-reported or objective moderate and poor hearing were more likely to have a dementia diagnosis than those with normal hearing (self-reported: odds ratio OR = 1.6, 95% CI = 1.1–2.4 moderate hearing; OR = 2.6, 95% CI = 1.7–3.9 poor hearing, objective: OR = 1.6, 95% CI = 1.0–2.8 moderate hearing; OR = 4.4, 95% CI = 1.9–9.9 poor hearing). Longitudinally, the hazard of developing dementia was 1.4 (95% CI = 1.0–1.9) times as high in individuals who reported moderate hearing and 1.6 (95% CI = 1.1–2.0) times as high in those who reported poor hearing.</p></div></div>
<div class="section" id="jgs14986-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Older adults with hearing loss are at greater risk of dementia than those with normal hearing. These findings are consistent with the rationale that correction of hearing loss could help delay the onset of dementia, or that hearing loss itself could serve as a risk indicator for cognitive decline.</p></div></div>
]]></content:encoded><description>

Objectives
To determine whether hearing loss is associated with incident physician-diagnosed dementia in a representative sample.


Design
Retrospective cohort study.


Setting
English Longitudinal Study of Ageing.


Participants
Adults aged 50 and older.


Measurements
Cross-sectional associations between self-reported (n = 7,865) and objective hearing measures (n = 6,902) and dementia were examined using multinomial-logistic regression. The longitudinal association between self-reported hearing at Wave 2 (2004/05) and cumulative physician-diagnosed dementia up to Wave 7 (2014/15) was modelled using Cox proportional hazards regression.


Results
After adjustment for potential confounders, in cross-sectional analysis, participants who had self-reported or objective moderate and poor hearing were more likely to have a dementia diagnosis than those with normal hearing (self-reported: odds ratio OR = 1.6, 95% CI = 1.1–2.4 moderate hearing; OR = 2.6, 95% CI = 1.7–3.9 poor hearing, objective: OR = 1.6, 95% CI = 1.0–2.8 moderate hearing; OR = 4.4, 95% CI = 1.9–9.9 poor hearing). Longitudinally, the hazard of developing dementia was 1.4 (95% CI = 1.0–1.9) times as high in individuals who reported moderate hearing and 1.6 (95% CI = 1.1–2.0) times as high in those who reported poor hearing.


Conclusion
Older adults with hearing loss are at greater risk of dementia than those with normal hearing. These findings are consistent with the rationale that correction of hearing loss could help delay the onset of dementia, or that hearing loss itself could serve as a risk indicator for cognitive decline.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14952" xmlns="http://purl.org/rss/1.0/"><title>Weight and Body Mass Index in Old Age: Do They Still Matter?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14952</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Weight and Body Mass Index in Old Age: Do They Still Matter?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tamara B. Harris</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-17T01:25:31.031522-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14952</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14952</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14952</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Editorial</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>This Editorial comments on the article by <a href="https://doi.org/10.1111/jgs.14790" rel="references:https://doi.org/10.1111/jgs.14790">Zhao Chen et al</a>.</p></div>
]]></content:encoded><description>
This Editorial comments on the article by Zhao Chen et al.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14999" xmlns="http://purl.org/rss/1.0/"><title>Reply to: Efficacy and Safety of Mechanical Thrombectomy in Older Adults with Acute Ischemic Stroke: Two Methodological Concerns</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14999</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Reply to: Efficacy and Safety of Mechanical Thrombectomy in Older Adults with Acute Ischemic Stroke: Two Methodological Concerns</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Caterina Motta, Giacomo Koch, Fabrizio Sallustio</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-17T01:10:19.009759-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14999</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14999</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14999</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>This letter comments on the Letter by <a href="https://doi.org/10.1111/jgs.14994" rel="references:https://doi.org/10.1111/jgs.14994">Safiri et al</a>.</p></div>
]]></content:encoded><description>
This letter comments on the Letter by Safiri et al.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14994" xmlns="http://purl.org/rss/1.0/"><title>Efficacy and Safety of Mechanical Thrombectomy in Older Adults with Acute Ischemic Stroke: Methodological Concerns</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14994</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Efficacy and Safety of Mechanical Thrombectomy in Older Adults with Acute Ischemic Stroke: Methodological Concerns</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Saeid Safiri, Mark J. M. Sullman, Erfan Ayubi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-17T01:10:17.8077-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14994</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14994</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14994</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>See the Reply by <a href="https://doi.org/10.1111/jgs.14999" rel="references:https://doi.org/10.1111/jgs.14999">Motta et al</a>.</p></div>
]]></content:encoded><description>
See the Reply by Motta et al.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14977" xmlns="http://purl.org/rss/1.0/"><title>The Birder</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14977</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The Birder</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Thomas J. Doyle</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-14T09:23:33.047649-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14977</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14977</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14977</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Old Lives Tale</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14984" xmlns="http://purl.org/rss/1.0/"><title>Reply to OverREACHing Conclusions</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14984</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Reply to OverREACHing Conclusions</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Linda O. Nichols, Jennifer Martindale-Adams, Carolyn W. Zhu, Erin K. Kaplan, Jeffrey K. Zuber, Jessica Lum, Teresa M. Waters</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-13T08:50:37.632199-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14984</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14984</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14984</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>This letter comments on the Letter by <a href="https://doi.org/10.1111/jgs.14949" rel="references:https://doi.org/10.1111/jgs.14949">William B. Weeks et al</a>.</p></div>
]]></content:encoded><description>
This letter comments on the Letter by William B. Weeks et al.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14949" xmlns="http://purl.org/rss/1.0/"><title>Over-REACHing Conclusions</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14949</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Over-REACHing Conclusions</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">William B. Weeks</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-13T08:50:33.545214-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14949</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14949</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14949</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>See the Reply by <a href="https://doi.org/10.1111/jgs.14984" rel="references:https://doi.org/10.1111/jgs.14984">Linda O. Nichols et al</a>.</p></div>
]]></content:encoded><description>
See the Reply by Linda O. Nichols et al.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14962" xmlns="http://purl.org/rss/1.0/"><title>Zika, Ebola, and Age: Global and Cellular Aging and Their Catalytic Effect on These Infections</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14962</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Zika, Ebola, and Age: Global and Cellular Aging and Their Catalytic Effect on These Infections</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Leslie S. Libow</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-13T08:50:19.302979-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14962</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14962</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14962</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14995" xmlns="http://purl.org/rss/1.0/"><title>The 2025 Big “G” Geriatrician: Defining Job Roles to Guide Fellowship Training</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14995</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The 2025 Big “G” Geriatrician: Defining Job Roles to Guide Fellowship Training</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Deborah Simpson, Rosanne M. Leipzig, Karen Sauvigné, </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-10T08:46:59.786486-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14995</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14995</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14995</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Education and Training</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Changes in health care that are already in progress, including value- and population-based care, use of new technologies for care, big data and machine learning, and the patient as consumer and decision maker, will determine the job description for geriatricians practicing in 2025. Informed by these future certainties, 115 geriatrics educators attending the 2016 Donald W. Reynolds Foundation Annual meeting identified five 2025 geriatrician job roles: complexivist; consultant; health system leader and innovator; functional preventionist; and educator for big “G” and little “g” providers. By identifying these job roles, geriatrics fellowship training can be preemptively redesigned.</p></div>
]]></content:encoded><description>
Changes in health care that are already in progress, including value- and population-based care, use of new technologies for care, big data and machine learning, and the patient as consumer and decision maker, will determine the job description for geriatricians practicing in 2025. Informed by these future certainties, 115 geriatrics educators attending the 2016 Donald W. Reynolds Foundation Annual meeting identified five 2025 geriatrician job roles: complexivist; consultant; health system leader and innovator; functional preventionist; and educator for big “G” and little “g” providers. By identifying these job roles, geriatrics fellowship training can be preemptively redesigned.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14996" xmlns="http://purl.org/rss/1.0/"><title>Big ‘G’ and Little ‘g’ Geriatrics Education for Physicians</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14996</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Big ‘G’ and Little ‘g’ Geriatrics Education for Physicians</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kathryn E. Callahan, Nina Tumosa, Rosanne M. Leipzig</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-10T08:40:21.960985-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14996</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14996</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14996</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Education and Training</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>In the July 2016 issue of this journal, Dr. Mary Tinetti proposed that geriatric medicine abandon attempts to increase the numbers of board-certified geriatricians and change focus to the development of a “small elite workforce.” What would be gained and what sacrificed by accepting this challenge? We agree that the best clinical use of a scarce resource, specialty trained geriatricians, is to care for frail, complex, severely ill elderly adults and to help design and study novel interventions in research, education, and care models to improve the care of all older adults, but for this to happen, all other providers must attain specific competency in the care of older adults. This article responds and discusses alternative pathways for teaching geriatrics care, training specialists, and geriatrics fellows.</p></div>
]]></content:encoded><description>
In the July 2016 issue of this journal, Dr. Mary Tinetti proposed that geriatric medicine abandon attempts to increase the numbers of board-certified geriatricians and change focus to the development of a “small elite workforce.” What would be gained and what sacrificed by accepting this challenge? We agree that the best clinical use of a scarce resource, specialty trained geriatricians, is to care for frail, complex, severely ill elderly adults and to help design and study novel interventions in research, education, and care models to improve the care of all older adults, but for this to happen, all other providers must attain specific competency in the care of older adults. This article responds and discusses alternative pathways for teaching geriatrics care, training specialists, and geriatrics fellows.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14934" xmlns="http://purl.org/rss/1.0/"><title>Robert L. Kane, MD (1940–2017)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14934</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Robert L. Kane, MD (1940–2017)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">James T. Pacala, Joseph G. Ouslander, Debra Saliba</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-07T22:00:45.246029-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14934</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14934</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14934</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Special Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14971" xmlns="http://purl.org/rss/1.0/"><title>Predictors of Independent Aging and Survival: A 16-Year Follow-Up Report in Octogenarian Men</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14971</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Predictors of Independent Aging and Survival: A 16-Year Follow-Up Report in Octogenarian Men</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kristin Franzon, Liisa Byberg, Per Sjögren, Björn Zethelius, Tommy Cederholm, Lena Kilander</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-07T01:01:00.532137-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14971</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14971</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14971</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14971-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To examine the longitudinal associations between aging with preserved functionality, i.e. independent aging and survival, and lifestyle variables, dietary pattern and cardiovascular risk factors.</p></div></div>
<div class="section" id="jgs14971-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Cohort study.</p></div></div>
<div class="section" id="jgs14971-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Uppsala Longitudinal Study of Adult Men, Sweden.</p></div></div>
<div class="section" id="jgs14971-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Swedish men (n = 1,104) at a mean age of 71 (range 69.4–74.1) were investigated, 369 of whom were evaluated for independent aging 16 years later, at a mean age of 87 (range 84.8–88.9).</p></div></div>
<div class="section" id="jgs14971-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>A questionnaire was used to obtain information on lifestyle, including education, living conditions, and physical activity. Adherence to a Mediterranean-like diet was assessed according to a modified Mediterranean Diet Score derived from 7-day food records. Cardiovascular risk factors were measured. Independent aging at a mean age of 87 was defined as lack of diagnosed dementia, a Mini-Mental State Examination score of 25 or greater, not institutionalized, independence in personal activities of daily living, and ability to walk outdoors alone. Complete survival data at age 85 were obtained from the Swedish Cause of Death Register.</p></div></div>
<div class="section" id="jgs14971-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Fifty-seven percent of the men survived to age 85, and 75% of the participants at a mean age of 87 displayed independent aging. Independent aging was associated with never smoking (vs current) (odds ratio (OR) = 2.20, 95% confidence interval (CI) = 1.05–4.60) and high (vs low) adherence to a Mediterranean-like diet (OR = 2.69, 95% CI = 1.14–6.80). Normal weight or overweight and waist circumference of 102 cm or less were also associated with independent aging. Similar associations were observed with survival.</p></div></div>
<div class="section" id="jgs14971-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Lifestyle factors such as never smoking, maintaining a healthy diet, and not being obese at age 71 were associated with survival and independent aging at age 85 and older in men.</p></div></div>
]]></content:encoded><description>

Objectives
To examine the longitudinal associations between aging with preserved functionality, i.e. independent aging and survival, and lifestyle variables, dietary pattern and cardiovascular risk factors.


Design
Cohort study.


Setting
Uppsala Longitudinal Study of Adult Men, Sweden.


Participants
Swedish men (n = 1,104) at a mean age of 71 (range 69.4–74.1) were investigated, 369 of whom were evaluated for independent aging 16 years later, at a mean age of 87 (range 84.8–88.9).


Measurements
A questionnaire was used to obtain information on lifestyle, including education, living conditions, and physical activity. Adherence to a Mediterranean-like diet was assessed according to a modified Mediterranean Diet Score derived from 7-day food records. Cardiovascular risk factors were measured. Independent aging at a mean age of 87 was defined as lack of diagnosed dementia, a Mini-Mental State Examination score of 25 or greater, not institutionalized, independence in personal activities of daily living, and ability to walk outdoors alone. Complete survival data at age 85 were obtained from the Swedish Cause of Death Register.


Results
Fifty-seven percent of the men survived to age 85, and 75% of the participants at a mean age of 87 displayed independent aging. Independent aging was associated with never smoking (vs current) (odds ratio (OR) = 2.20, 95% confidence interval (CI) = 1.05–4.60) and high (vs low) adherence to a Mediterranean-like diet (OR = 2.69, 95% CI = 1.14–6.80). Normal weight or overweight and waist circumference of 102 cm or less were also associated with independent aging. Similar associations were observed with survival.


Conclusion
Lifestyle factors such as never smoking, maintaining a healthy diet, and not being obese at age 71 were associated with survival and independent aging at age 85 and older in men.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14992" xmlns="http://purl.org/rss/1.0/"><title>The Past Is How We Live the Future</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14992</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The Past Is How We Live the Future</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Paul Rousseau</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-06T09:55:18.149724-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14992</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14992</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14992</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Old Lives Tale</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14954" xmlns="http://purl.org/rss/1.0/"><title>How Hospital Clinicians Select Patients for Skilled Nursing Facilities</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14954</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">How Hospital Clinicians Select Patients for Skilled Nursing Facilities</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Robert E. Burke, Emily Lawrence, Amy Ladebue, Roman Ayele, Brandi Lippmann, Ethan Cumbler, Rebecca Allyn, Jacqueline Jones</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-06T09:55:12.033092-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14954</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14954</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14954</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14954-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To understand how hospital-based clinicians evaluate older adults in the hospital and decide who will be transferred to a skilled nursing facility (SNF) for postacute care.</p></div></div>
<div class="section" id="jgs14954-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Semistructured interviews paired with a qualitative analytical approach informed by Social Constructivist theory.</p></div></div>
<div class="section" id="jgs14954-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Inpatient care units in three hospitals. Purposive sampling was used to maximize variability in hospitals, units within hospitals, and staff on those units.</p></div></div>
<div class="section" id="jgs14954-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Clinicians (hospitalists, nurses, therapists, social workers, case managers) involved in evaluation and decision-making regarding postacute care (N = 25).</p></div></div>
<div class="section" id="jgs14954-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Central themes related to clinician evaluation and discharge decision-making.</p></div></div>
<div class="section" id="jgs14954-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Clinicians described pressure to expedite evaluation and discharge decisions, resulting in the use of SNFs as a “safety net” for older adults being discharged from the hospital. The lack of hospital-based clinician knowledge of SNF care practices, quality, or patient outcomes resulted in lack of a standardized evaluation process or a clear primary decision-maker.</p></div></div>
<div class="section" id="jgs14954-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Hospital clinician evaluation and decision-making about postacute care in SNFs may be characterized as rushed, without a clear system or framework for making decisions and uninformed by knowledge of SNF or patient outcomes in those discharged to SNFs. This leads to SNFs being used as a “safety net” for many older adults. As hospitals and SNFs are increasingly held jointly accountable for outcomes of individuals transitioning between hospitals and SNFs, novel solutions for improving evaluation and decision-making are urgently needed.</p></div></div>
]]></content:encoded><description>

Objective
To understand how hospital-based clinicians evaluate older adults in the hospital and decide who will be transferred to a skilled nursing facility (SNF) for postacute care.


Design
Semistructured interviews paired with a qualitative analytical approach informed by Social Constructivist theory.


Setting
Inpatient care units in three hospitals. Purposive sampling was used to maximize variability in hospitals, units within hospitals, and staff on those units.


Participants
Clinicians (hospitalists, nurses, therapists, social workers, case managers) involved in evaluation and decision-making regarding postacute care (N = 25).


Measurements
Central themes related to clinician evaluation and discharge decision-making.


Results
Clinicians described pressure to expedite evaluation and discharge decisions, resulting in the use of SNFs as a “safety net” for older adults being discharged from the hospital. The lack of hospital-based clinician knowledge of SNF care practices, quality, or patient outcomes resulted in lack of a standardized evaluation process or a clear primary decision-maker.


Conclusion
Hospital clinician evaluation and decision-making about postacute care in SNFs may be characterized as rushed, without a clear system or framework for making decisions and uninformed by knowledge of SNF or patient outcomes in those discharged to SNFs. This leads to SNFs being used as a “safety net” for many older adults. As hospitals and SNFs are increasingly held jointly accountable for outcomes of individuals transitioning between hospitals and SNFs, novel solutions for improving evaluation and decision-making are urgently needed.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14988" xmlns="http://purl.org/rss/1.0/"><title>Selecting a Skilled Nursing Facility for Postacute Care: Individual and Family Perspectives</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14988</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Selecting a Skilled Nursing Facility for Postacute Care: Individual and Family Perspectives</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Emily A. Gadbois, Denise A. Tyler, Vincent Mor</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-06T09:54:45.364304-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14988</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14988</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14988</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14988-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To describe individuals' experiences during the hospital discharge planning and skilled nursing facility (SNF) selection process.</p></div></div>
<div class="section" id="jgs14988-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Semistructured interviews focusing on discharge planning and nursing facility selection, including how facilities were chosen, who was involved, and what factors were important in decision-making.</p></div></div>
<div class="section" id="jgs14988-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>14 SNFs in five cities across the United States.</p></div></div>
<div class="section" id="jgs14988-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Newly admitted, previously community-dwelling SNF residents (N = 98) and their family members.</p></div></div>
<div class="section" id="jgs14988-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurement</h4><div class="para"><p>Semistructured interviews were qualitatively coded to identify underlying themes.</p></div></div>
<div class="section" id="jgs14988-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Most respondents reported receiving only a list of SNF names and addresses from discharge planners and that hospital staff were minimally involved. Proximity to home and prior experience with the facility most often influenced choice of SNF. Most respondents reported being satisfied with their placement, although many stated that they would have been willing to travel further to another SNF were it recommended. Many reported feeling rushed and unprepared, stating that they did not know where or how to get help.</p></div></div>
<div class="section" id="jgs14988-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>SNF placement is a stressful transition, occurring when people are physically vulnerable and with limited guidance from discharge planners. Therefore, most people select a facility based on its location, perhaps because they are provided with no other information. Given Centers for Medicare and Medicaid Services' proposed changes to the discharge planning process, this research highlights the value of providing people and family caregivers with quality data and assistance in interpreting it.</p></div></div>
]]></content:encoded><description>

Objectives
To describe individuals' experiences during the hospital discharge planning and skilled nursing facility (SNF) selection process.


Design
Semistructured interviews focusing on discharge planning and nursing facility selection, including how facilities were chosen, who was involved, and what factors were important in decision-making.


Setting
14 SNFs in five cities across the United States.


Participants
Newly admitted, previously community-dwelling SNF residents (N = 98) and their family members.


Measurement
Semistructured interviews were qualitatively coded to identify underlying themes.


Results
Most respondents reported receiving only a list of SNF names and addresses from discharge planners and that hospital staff were minimally involved. Proximity to home and prior experience with the facility most often influenced choice of SNF. Most respondents reported being satisfied with their placement, although many stated that they would have been willing to travel further to another SNF were it recommended. Many reported feeling rushed and unprepared, stating that they did not know where or how to get help.


Conclusion
SNF placement is a stressful transition, occurring when people are physically vulnerable and with limited guidance from discharge planners. Therefore, most people select a facility based on its location, perhaps because they are provided with no other information. Given Centers for Medicare and Medicaid Services' proposed changes to the discharge planning process, this research highlights the value of providing people and family caregivers with quality data and assistance in interpreting it.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14989" xmlns="http://purl.org/rss/1.0/"><title>Need to Recalibrate Research Outcomes in Alzheimer's Disease: Focus on Neuropsychiatric Symptoms</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14989</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Need to Recalibrate Research Outcomes in Alzheimer's Disease: Focus on Neuropsychiatric Symptoms</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marco Canevelli, Matteo Cesari, Flaminia Lucchini, Martina Valletta, Michele Sabino, Eleonora Lacorte, Nicola Vanacore, Giuseppe Bruno</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-06T09:48:09.424378-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14989</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14989</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14989</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Brief Report</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14989-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To determine whether neuropsychiatric symptoms (NPSs) are adequately considered in clinical research on Alzheimer's disease (AD).</p></div></div>
<div class="section" id="jgs14989-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Systematic review.</p></div></div>
<div class="section" id="jgs14989-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Randomized controlled trials (RCTs) recruiting individuals with AD and published during the last 10 years in 16 major general medicine, neurology, psychiatry, and geriatric psychiatry journals and RCTs registered on clinicaltrials.gov and currently enrolling individuals with AD.</p></div></div>
<div class="section" id="jgs14989-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Individuals with AD.</p></div></div>
<div class="section" id="jgs14989-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Outcome measures adopted by the included studies.</p></div></div>
<div class="section" id="jgs14989-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Only 21.4% of the included studies identified through the bibliographic searches had measures of NPSs as a primary outcome. Only 17.7% of the studies retrieved on clinicaltrials.gov made a specific effort to test the effect of pharmacological or nonpharmacological interventions on NPSs.</p></div></div>
<div class="section" id="jgs14989-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>These findings show how rarely previous and current research on AD has considered NPSs as primary research targets. Although these symptoms are widely recognized as the most-stressful and -challenging manifestations of dementia, they are addressed much less often than other research targets.</p></div></div>
]]></content:encoded><description>

Objectives
To determine whether neuropsychiatric symptoms (NPSs) are adequately considered in clinical research on Alzheimer's disease (AD).


Design
Systematic review.


Setting
Randomized controlled trials (RCTs) recruiting individuals with AD and published during the last 10 years in 16 major general medicine, neurology, psychiatry, and geriatric psychiatry journals and RCTs registered on clinicaltrials.gov and currently enrolling individuals with AD.


Participants
Individuals with AD.


Measurements
Outcome measures adopted by the included studies.


Results
Only 21.4% of the included studies identified through the bibliographic searches had measures of NPSs as a primary outcome. Only 17.7% of the studies retrieved on clinicaltrials.gov made a specific effort to test the effect of pharmacological or nonpharmacological interventions on NPSs.


Conclusion
These findings show how rarely previous and current research on AD has considered NPSs as primary research targets. Although these symptoms are widely recognized as the most-stressful and -challenging manifestations of dementia, they are addressed much less often than other research targets.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14904" xmlns="http://purl.org/rss/1.0/"><title>Rates of Delirium Diagnosis Do Not Improve with Emergency Risk Screening: Results of the Emergency Department Delirium Initiative Trial</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14904</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Rates of Delirium Diagnosis Do Not Improve with Emergency Risk Screening: Results of the Emergency Department Delirium Initiative Trial</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Glenn Arendts, Jennefer Love, Yusuf Nagree, David Bruce, Malcolm Hare, Ian Dey</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-04T09:35:30.629593-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14904</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14904</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14904</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14904-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To determine whether a bundled risk screening and warning or action card system improves formal delirium diagnosis and person-centered outcomes in hospitalized older adults.</p></div></div>
<div class="section" id="jgs14904-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Prospective trial with sequential introduction of screening and interventional processes.</p></div></div>
<div class="section" id="jgs14904-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Two tertiary referral hospitals in Australia.</p></div></div>
<div class="section" id="jgs14904-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Individuals aged 65 and older presenting to the emergency department (ED) and not requiring immediate resuscitation (N = 3,905).</p></div></div>
<div class="section" id="jgs14904-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Intervention</h4><div class="para"><p>Formal ED delirium screening algorithm and use of a risk warning card with a recommended series of actions for the prevention and management of delirium during the subsequent admission</p></div></div>
<div class="section" id="jgs14904-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Delirium diagnosis at hospital discharge, proportion discharged to new assisted living arrangements, in-hospital complications (use of sedation, falls, aspiration pneumonia, death), hospital length of stay.</p></div></div>
<div class="section" id="jgs14904-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Participants with a positive risk screen were significantly more likely (relative risk = 6.0, 95% confidence interval = 4.9–7.3) to develop delirium, and the proportion of at-risk participants with a positive screen was constant across three study phases. Delirium detection rate in participants undergoing the final intervention (Phase 3) was 12.1% (a 2% absolute and 17% relative increase from the baseline rate) but this was not statistically significant (<em>P</em> = .29), and a similar relative increase was seen over time in participants not receiving the intervention</p></div></div>
<div class="section" id="jgs14904-sec-0008" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>A risk screening and warning or action card intervention in the ED did not significantly improve rates of delirium detection or other important outcomes.</p></div></div>
]]></content:encoded><description>

Objectives
To determine whether a bundled risk screening and warning or action card system improves formal delirium diagnosis and person-centered outcomes in hospitalized older adults.


Design
Prospective trial with sequential introduction of screening and interventional processes.


Setting
Two tertiary referral hospitals in Australia.


Participants
Individuals aged 65 and older presenting to the emergency department (ED) and not requiring immediate resuscitation (N = 3,905).


Intervention
Formal ED delirium screening algorithm and use of a risk warning card with a recommended series of actions for the prevention and management of delirium during the subsequent admission


Measurements
Delirium diagnosis at hospital discharge, proportion discharged to new assisted living arrangements, in-hospital complications (use of sedation, falls, aspiration pneumonia, death), hospital length of stay.


Results
Participants with a positive risk screen were significantly more likely (relative risk = 6.0, 95% confidence interval = 4.9–7.3) to develop delirium, and the proportion of at-risk participants with a positive screen was constant across three study phases. Delirium detection rate in participants undergoing the final intervention (Phase 3) was 12.1% (a 2% absolute and 17% relative increase from the baseline rate) but this was not statistically significant (P = .29), and a similar relative increase was seen over time in participants not receiving the intervention


Conclusion
A risk screening and warning or action card intervention in the ED did not significantly improve rates of delirium detection or other important outcomes.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14991" xmlns="http://purl.org/rss/1.0/"><title>Associations Between Self-Reported Physical Activity and Physical Performance Measures Over Time in Postmenopausal Women: The Women's Health Initiative</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14991</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Associations Between Self-Reported Physical Activity and Physical Performance Measures Over Time in Postmenopausal Women: The Women's Health Initiative</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Deepika R. Laddu, Betsy C. Wertheim, David O. Garcia, Robert Brunner, Erik Groessl, Aladdin H. Shadyab, Scott B. Going, Michael J. LaMonte, Brad Cannell, Meryl S. LeBoff, Jane A. Cauley, Cynthia A. Thomson, Marcia L. Stefanick</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-04T09:35:26.776441-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14991</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14991</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14991</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14991-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To examine prospective associations between changes in physical activity (PA) and changes in physical performance measures (PPMs) over 6 years in older women.</p></div></div>
<div class="section" id="jgs14991-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Prospective cohort study.</p></div></div>
<div class="section" id="jgs14991-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Forty clinical centers in the United States.</p></div></div>
<div class="section" id="jgs14991-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Women aged 65 and older (mean age 69.8) enrolled in the Women's Health Initiative Clinical Trials with gait speed, timed chair stand, grip strength, and self-reported recreational PA data assessed at baseline (1993–98) and follow-up Years 1, 3, and 6 (N = 5,092).</p></div></div>
<div class="section" id="jgs14991-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Mixed-effects linear regression models were used to determine the association between time-varying PA and change in each PPM. Potential interactions between time-varying PA and age (&lt;70, ≥70) were also tested.</p></div></div>
<div class="section" id="jgs14991-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Significan, dose-response associations between PA and improvements in all PPMs were observed over the 6 years of follow-up after adjusting for important covariates. High PA groups (≥1,200 metabolic equivalent (MET)-min/wk) had stronger grip strength (0.48 kg greater; <em>P</em> &lt; .01), more chair stands (0.35 more; <em>P</em> &lt; .001), and faster gait speeds (0.06 m/s faster; <em>P</em> &lt; .001) than sedentary women (&lt;100 MET-min/wk). Higher PA levels were associated with a greater increase in chair stands over time in women aged 70 and older (<em>P</em> &lt; .001) than in those younger than 70 (<em>P</em><sub>interaction for age</sub> = .01).</p></div></div>
<div class="section" id="jgs14991-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>In postmenopausal women, maintaining high PA levels over time is associated with better lower extremity function. These data support the view that regular PA plays an important role in maintaining functional status during aging in older women.</p></div></div>
]]></content:encoded><description>

Objectives
To examine prospective associations between changes in physical activity (PA) and changes in physical performance measures (PPMs) over 6 years in older women.


Design
Prospective cohort study.


Setting
Forty clinical centers in the United States.


Participants
Women aged 65 and older (mean age 69.8) enrolled in the Women's Health Initiative Clinical Trials with gait speed, timed chair stand, grip strength, and self-reported recreational PA data assessed at baseline (1993–98) and follow-up Years 1, 3, and 6 (N = 5,092).


Measurements
Mixed-effects linear regression models were used to determine the association between time-varying PA and change in each PPM. Potential interactions between time-varying PA and age (&lt;70, ≥70) were also tested.


Results
Significan, dose-response associations between PA and improvements in all PPMs were observed over the 6 years of follow-up after adjusting for important covariates. High PA groups (≥1,200 metabolic equivalent (MET)-min/wk) had stronger grip strength (0.48 kg greater; P &lt; .01), more chair stands (0.35 more; P &lt; .001), and faster gait speeds (0.06 m/s faster; P &lt; .001) than sedentary women (&lt;100 MET-min/wk). Higher PA levels were associated with a greater increase in chair stands over time in women aged 70 and older (P &lt; .001) than in those younger than 70 (Pinteraction for age = .01).


Conclusion
In postmenopausal women, maintaining high PA levels over time is associated with better lower extremity function. These data support the view that regular PA plays an important role in maintaining functional status during aging in older women.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14983" xmlns="http://purl.org/rss/1.0/"><title>A Cumulative Deficit Laboratory Test–based Frailty Index: Personal and Neighborhood Associations</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14983</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A Cumulative Deficit Laboratory Test–based Frailty Index: Personal and Neighborhood Associations</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Katherine E. King, Gerda G. Fillenbaum, Harvey J. Cohen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-30T08:00:20.354423-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14983</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14983</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14983</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14983-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To explore the association between a newly developed cumulative laboratory-based frailty index (FI) and intrinsic (personal) and extrinsic (social, environmental) characteristics.</p></div></div>
<div class="section" id="jgs14983-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Cross-sectional longitudinal study.</p></div></div>
<div class="section" id="jgs14983-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>The third and fourth waves of the community-representative, five-county, 10-year Duke Established Populations for Epidemiologic Studies of the Elderly study, carried out in a health service-rich area.</p></div></div>
<div class="section" id="jgs14983-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Cognitively intact survivors of the third wave (N = 1,740), who provided blood samples for standard laboratory work.</p></div></div>
<div class="section" id="jgs14983-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Biomarkers (n = 28) were measured to develop a cumulative deficit laboratory test–based FI (Duke FI) derived from standard laboratory tests: SMAC-24 chemistry panel, high-density lipoprotein cholesterol panel, and complete blood count. Information was gathered on scales assessing intrinsic characteristics (personal locus of control, life satisfaction, self-esteem, depressive symptomatology) and extrinsic characteristics (support received from and provided to family and friends, stressful life events, neighborhood disadvantage).</p></div></div>
<div class="section" id="jgs14983-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The newly developed Duke FI had content, construct, concurrent, and predictive validity. In addition to sex, race, and income, the Duke FI was associated at the intrinsic level with locus of control, self-esteem, life satisfaction, and depressive symptomatology (each <em>P</em> &lt; .01) and at the extrinsic level with provision (<em>P</em> &lt; .01) and with receipt of instrumental help (<em>P</em> &lt; .10), social stressors (<em>P</em> &lt; .03), and neighborhood disadvantage (<em>P</em> &lt; .01) in unadjusted analysis; race fully explained neighborhood disadvantage.</p></div></div>
<div class="section" id="jgs14983-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Intrinsic (personality) characteristics and personally close extrinsic characteristics (contacts with family and friends, personal stressors) are associated with laboratory test–based frailty, as is neighborhood disadvantage, although in this accessible, health service–rich environment, race fully explained association with neighborhood disadvantage, suggesting that interventions to reduce frailty in residents in such an environment should pay particular attention to characteristics that immediately affect the individual.</p></div></div>
]]></content:encoded><description>

Objectives
To explore the association between a newly developed cumulative laboratory-based frailty index (FI) and intrinsic (personal) and extrinsic (social, environmental) characteristics.


Design
Cross-sectional longitudinal study.


Setting
The third and fourth waves of the community-representative, five-county, 10-year Duke Established Populations for Epidemiologic Studies of the Elderly study, carried out in a health service-rich area.


Participants
Cognitively intact survivors of the third wave (N = 1,740), who provided blood samples for standard laboratory work.


Measurements
Biomarkers (n = 28) were measured to develop a cumulative deficit laboratory test–based FI (Duke FI) derived from standard laboratory tests: SMAC-24 chemistry panel, high-density lipoprotein cholesterol panel, and complete blood count. Information was gathered on scales assessing intrinsic characteristics (personal locus of control, life satisfaction, self-esteem, depressive symptomatology) and extrinsic characteristics (support received from and provided to family and friends, stressful life events, neighborhood disadvantage).


Results
The newly developed Duke FI had content, construct, concurrent, and predictive validity. In addition to sex, race, and income, the Duke FI was associated at the intrinsic level with locus of control, self-esteem, life satisfaction, and depressive symptomatology (each P &lt; .01) and at the extrinsic level with provision (P &lt; .01) and with receipt of instrumental help (P &lt; .10), social stressors (P &lt; .03), and neighborhood disadvantage (P &lt; .01) in unadjusted analysis; race fully explained neighborhood disadvantage.


Conclusion
Intrinsic (personality) characteristics and personally close extrinsic characteristics (contacts with family and friends, personal stressors) are associated with laboratory test–based frailty, as is neighborhood disadvantage, although in this accessible, health service–rich environment, race fully explained association with neighborhood disadvantage, suggesting that interventions to reduce frailty in residents in such an environment should pay particular attention to characteristics that immediately affect the individual.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14927" xmlns="http://purl.org/rss/1.0/"><title>Treatment of Sarcopenia with Bimagrumab: Results from a Phase II, Randomized, Controlled, Proof-of-Concept Study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14927</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Treatment of Sarcopenia with Bimagrumab: Results from a Phase II, Randomized, Controlled, Proof-of-Concept Study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Daniel Rooks, Jens Praestgaard, Sam Hariry, Didier Laurent, Olivier Petricoul, Robert G. Perry, Estelle Lach-Trifilieff, Ronenn Roubenoff</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-27T01:07:45.501944-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14927</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14927</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14927</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14927-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To assess the effects of bimagrumab on skeletal muscle mass and function in older adults with sarcopenia and mobility limitations.</p></div></div>
<div class="section" id="jgs14927-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>A 24-week, randomized, double-blind, placebo-controlled, parallel-arm, proof-of-concept study.</p></div></div>
<div class="section" id="jgs14927-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Five centers in the United States.</p></div></div>
<div class="section" id="jgs14927-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Community-dwelling adults (N = 40) aged 65 and older with gait speed between 0.4 and 1.0 m/s over 4 m and an appendicular skeletal muscle index of 7.25 kg/m<sup>2</sup> or less for men and 5.67 kg/m<sup>2</sup> or less for women.</p></div></div>
<div class="section" id="jgs14927-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Intervention</h4><div class="para"><p>Intravenous bimagrumab 30 mg/kg (n = 19) or placebo (n = 21).</p></div></div>
<div class="section" id="jgs14927-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Change from baseline in thigh muscle volume (TMV), subcutaneous and intermuscular fat, appendicular and total lean body mass, grip strength, gait speed, and 6-minute walk distance (6MWD).</p></div></div>
<div class="section" id="jgs14927-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Thirty-two (80%) participants completed the study. TMV increased by Week 2, was sustained throughout the treatment period, and remained above baseline at the end of study in bimagrumab-treated participants, whereas there was no change with placebo treatment (Week 2: 5.15 ± 2.19% vs −0.34 ± 2.59%, <em>P</em> &lt; .001; Week 4: 6.12 ± 2.56% vs 0.16 ± 3.42%, <em>P</em> &lt; .001; Week 8: 8.01 ± 3.70% vs 0.35 ± 3.32%, <em>P</em> &lt; .001; Week 16: 7.72 ± 5.31% vs 0.42 ± 5.14%, <em>P</em> &lt; .001; Week 24: 4.80 ± 5.81% vs −1.01 ± 4.43%, <em>P</em> = .002). Participants with slower walking speed at baseline receiving bimagrumab had clinically meaningful and statistically significantly greater improvements in gait speed (mean 0.15 m/s, <em>P</em> = .009) and 6MWD (mean 82 m, <em>P</em> = .022) than those receiving placebo at Week 16. Adverse events in the bimagrumab group included muscle-related symptoms, acne, and diarrhea, most of which were mild in severity and resolved by the end of study.</p></div></div>
<div class="section" id="jgs14927-sec-0008" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Treatment with bimagrumab over 16 weeks increased muscle mass and strength in older adults with sarcopenia and improved mobility in those with slow walking speed.</p></div></div>
]]></content:encoded><description>

Objectives
To assess the effects of bimagrumab on skeletal muscle mass and function in older adults with sarcopenia and mobility limitations.


Design
A 24-week, randomized, double-blind, placebo-controlled, parallel-arm, proof-of-concept study.


Setting
Five centers in the United States.


Participants
Community-dwelling adults (N = 40) aged 65 and older with gait speed between 0.4 and 1.0 m/s over 4 m and an appendicular skeletal muscle index of 7.25 kg/m2 or less for men and 5.67 kg/m2 or less for women.


Intervention
Intravenous bimagrumab 30 mg/kg (n = 19) or placebo (n = 21).


Measurements
Change from baseline in thigh muscle volume (TMV), subcutaneous and intermuscular fat, appendicular and total lean body mass, grip strength, gait speed, and 6-minute walk distance (6MWD).


Results
Thirty-two (80%) participants completed the study. TMV increased by Week 2, was sustained throughout the treatment period, and remained above baseline at the end of study in bimagrumab-treated participants, whereas there was no change with placebo treatment (Week 2: 5.15 ± 2.19% vs −0.34 ± 2.59%, P &lt; .001; Week 4: 6.12 ± 2.56% vs 0.16 ± 3.42%, P &lt; .001; Week 8: 8.01 ± 3.70% vs 0.35 ± 3.32%, P &lt; .001; Week 16: 7.72 ± 5.31% vs 0.42 ± 5.14%, P &lt; .001; Week 24: 4.80 ± 5.81% vs −1.01 ± 4.43%, P = .002). Participants with slower walking speed at baseline receiving bimagrumab had clinically meaningful and statistically significantly greater improvements in gait speed (mean 0.15 m/s, P = .009) and 6MWD (mean 82 m, P = .022) than those receiving placebo at Week 16. Adverse events in the bimagrumab group included muscle-related symptoms, acne, and diarrhea, most of which were mild in severity and resolved by the end of study.


Conclusion
Treatment with bimagrumab over 16 weeks increased muscle mass and strength in older adults with sarcopenia and improved mobility in those with slow walking speed.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14961" xmlns="http://purl.org/rss/1.0/"><title>Improving Management of Urinary Tract Infections in Older Adults: A Paradigm Shift or Therapeutic Nihilism?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14961</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Improving Management of Urinary Tract Infections in Older Adults: A Paradigm Shift or Therapeutic Nihilism?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christopher J. Crnich, Robin L. Jump, David A. Nace</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-27T01:07:39.869279-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14961</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14961</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14961</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Editorial</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14957" xmlns="http://purl.org/rss/1.0/"><title>Polypharmacy and Gait Performance in Community–dwelling Older Adults</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14957</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Polypharmacy and Gait Performance in Community–dwelling Older Adults</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Claudene George, Joe Verghese</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-26T01:01:00.901448-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14957</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14957</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14957</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Drugs &amp; Pharmacology</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14957-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To examine the relationship between polypharmacy and gait performance during simple (normal walk (NW)) and complex (walking while talking (WWT)) locomotion.</p></div></div>
<div class="section" id="jgs14957-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Cross-sectional.</p></div></div>
<div class="section" id="jgs14957-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Community.</p></div></div>
<div class="section" id="jgs14957-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Community-dwelling older adults (N = 482).</p></div></div>
<div class="section" id="jgs14957-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Polypharmacy, defined as use of five or more medications and a cohort-specific alternate definition of eight or more medications, was examined. Velocity (cm/s) measured quantitatively during NW and WWT conditions.</p></div></div>
<div class="section" id="jgs14957-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The 164 participants (34%) with polypharmacy of five or more medications were older (77.0 ± 6.6 vs 76.0 ± 6.4) and more likely to have hypertension, congestive heart failure, diabetes mellitus, myocardial infarction, and higher body mass index (BMI) and to have fallen within the last year than the remaining 318 without polypharmacy and walked 6 cm/s slower (<em>P</em> = .004) during NW and 4 cm/s slower during WWT (<em>P</em> = .07), adjusting for age, sex, and education. Group differences were not statistically significant after adjusting for comorbidities. Prevalence of polypharmacy of eight or more medications was 10%. This group walked 11 cm/s slower during NW (<em>P</em> &lt; .001) and 8.6 cm/s slower during WWT (<em>P</em> = .01) than those without polypharmacy, adjusted for age, sex, and education. Participants taking eight or more medications had slower NW (8.5 cm/s; <em>P</em> = .01), and WWT (6.9 cm/s; <em>P</em> = .07), compared to those without polypharmacy, adjusting for comorbidities. Adjustments for BMI, high-risk drugs, falls, and comorbidities yielded slower NW (9.4 cm/s, <em>P</em> = .005) and WWT (7.9 cm/s, <em>P</em> = .04 among those with polypharmacy compared to those without polypharmacy).</p></div></div>
<div class="section" id="jgs14957-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>These results suggest an association between polypharmacy and locomotion that medical comorbidities only partly explained.</p></div></div>
]]></content:encoded><description>

Objectives
To examine the relationship between polypharmacy and gait performance during simple (normal walk (NW)) and complex (walking while talking (WWT)) locomotion.


Design
Cross-sectional.


Setting
Community.


Participants
Community-dwelling older adults (N = 482).


Measurements
Polypharmacy, defined as use of five or more medications and a cohort-specific alternate definition of eight or more medications, was examined. Velocity (cm/s) measured quantitatively during NW and WWT conditions.


Results
The 164 participants (34%) with polypharmacy of five or more medications were older (77.0 ± 6.6 vs 76.0 ± 6.4) and more likely to have hypertension, congestive heart failure, diabetes mellitus, myocardial infarction, and higher body mass index (BMI) and to have fallen within the last year than the remaining 318 without polypharmacy and walked 6 cm/s slower (P = .004) during NW and 4 cm/s slower during WWT (P = .07), adjusting for age, sex, and education. Group differences were not statistically significant after adjusting for comorbidities. Prevalence of polypharmacy of eight or more medications was 10%. This group walked 11 cm/s slower during NW (P &lt; .001) and 8.6 cm/s slower during WWT (P = .01) than those without polypharmacy, adjusted for age, sex, and education. Participants taking eight or more medications had slower NW (8.5 cm/s; P = .01), and WWT (6.9 cm/s; P = .07), compared to those without polypharmacy, adjusting for comorbidities. Adjustments for BMI, high-risk drugs, falls, and comorbidities yielded slower NW (9.4 cm/s, P = .005) and WWT (7.9 cm/s, P = .04 among those with polypharmacy compared to those without polypharmacy).


Conclusion
These results suggest an association between polypharmacy and locomotion that medical comorbidities only partly explained.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14938" xmlns="http://purl.org/rss/1.0/"><title>StaRI Aims to Overcome Knowledge Translation Inertia: The Standards for Reporting Implementation Studies Guidelines</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14938</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">StaRI Aims to Overcome Knowledge Translation Inertia: The Standards for Reporting Implementation Studies Guidelines</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christopher R. Carpenter, Hilary Pinnock</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-26T00:58:34.430902-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14938</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14938</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14938</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Editorial</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14917" xmlns="http://purl.org/rss/1.0/"><title>Comment On: Geriatricians: The Super Specialist</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14917</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comment On: Geriatricians: The Super Specialist</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Benny Katz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-23T09:40:18.696785-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14917</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14917</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14917</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14980" xmlns="http://purl.org/rss/1.0/"><title>Catechol-O-Methyltransferase Genotype and Gait Speed Changes over 10 Years in Older Adults</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14980</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Catechol-O-Methyltransferase Genotype and Gait Speed Changes over 10 Years in Older Adults</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Andrea L. Metti, Caterina Rosano, Robert Boudreau, Robyn Massa, Kristine Yaffe, Suzanne Satterfield, Tamara Harris, Andrea L. Rosso</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-22T09:08:07.706904-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14980</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14980</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14980</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14980-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To determine the association between catechol-O-methyltransferase (COMT) genotype and 6-m walk time and to determine whether these associations are quadratic in nature, similar to previously reported U-shaped associations between dopamine and gait and cognition.</p></div></div>
<div class="section" id="jgs14980-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Prospective cohort study.</p></div></div>
<div class="section" id="jgs14980-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Health, Aging and Body Composition Study.</p></div></div>
<div class="section" id="jgs14980-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Black (n = 850) and white (n = 1,352) men and women with a mean age of 73.5 ± 2.85 at baseline.</p></div></div>
<div class="section" id="jgs14980-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Mixed models were used to assess the association between the COMT genotype and 6-m walk time, cross-sectionally and longitudinally over 10 years. Models were assessed unstratified and stratified according to race because allele distributions were different between white and black participants.</p></div></div>
<div class="section" id="jgs14980-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>There was a significant U-shaped association between COMT genotype and 6-m walk time: those with higher (Val/Val) and lower (Met/Met) dopamine slowed more over 10 years (0.22 ± 0.02 seconds per visit and 0.23 ± 0.02 seconds per visit, respectively) than those with the intermediate (Met/Val) dopamine (0.20 ± 0.02 seconds per visit) (<em>P</em> = .005). Stratified results showed a significant relationship in black (<em>P</em> = .01) but not white (<em>P</em> = .15) participants.</p></div></div>
<div class="section" id="jgs14980-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>These findings indicate a role of dopaminergic regulation of gait speed in community-dwelling older adults and of prefrontal cortex involvement in gait performance. Future work should investigate the molecular integrity of dopaminergic networks and gait changes over time and structural changes in the brain with COMT and gait decline in older adults.</p></div></div>
]]></content:encoded><description>

Objectives
To determine the association between catechol-O-methyltransferase (COMT) genotype and 6-m walk time and to determine whether these associations are quadratic in nature, similar to previously reported U-shaped associations between dopamine and gait and cognition.


Design
Prospective cohort study.


Setting
Health, Aging and Body Composition Study.


Participants
Black (n = 850) and white (n = 1,352) men and women with a mean age of 73.5 ± 2.85 at baseline.


Measurements
Mixed models were used to assess the association between the COMT genotype and 6-m walk time, cross-sectionally and longitudinally over 10 years. Models were assessed unstratified and stratified according to race because allele distributions were different between white and black participants.


Results
There was a significant U-shaped association between COMT genotype and 6-m walk time: those with higher (Val/Val) and lower (Met/Met) dopamine slowed more over 10 years (0.22 ± 0.02 seconds per visit and 0.23 ± 0.02 seconds per visit, respectively) than those with the intermediate (Met/Val) dopamine (0.20 ± 0.02 seconds per visit) (P = .005). Stratified results showed a significant relationship in black (P = .01) but not white (P = .15) participants.


Conclusion
These findings indicate a role of dopaminergic regulation of gait speed in community-dwelling older adults and of prefrontal cortex involvement in gait performance. Future work should investigate the molecular integrity of dopaminergic networks and gait changes over time and structural changes in the brain with COMT and gait decline in older adults.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14955" xmlns="http://purl.org/rss/1.0/"><title>Functional Impairment: An Unmeasured Marker of Medicare Costs for Postacute Care of Older Adults</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14955</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Functional Impairment: An Unmeasured Marker of Medicare Costs for Postacute Care of Older Adults</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. Ryan Greysen, Irena Stijacic Cenzer, W. John Boscardin, Kenneth E. Covinsky</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-21T09:30:33.534685-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14955</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14955</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14955</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14955-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To assess the effects of preadmission functional impairment on Medicare costs of postacute care up to 365 days after hospital discharge.</p></div></div>
<div class="section" id="jgs14955-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Longitudinal cohort study.</p></div></div>
<div class="section" id="jgs14955-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Health and Retirement Study (HRS).</p></div></div>
<div class="section" id="jgs14955-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Nationally representative sample of 16,673 Medicare hospitalizations of 8,559 community-dwelling older adults from 2000 to 2012.</p></div></div>
<div class="section" id="jgs14955-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>The main outcome was total Medicare costs in the year after hospital discharge, assessed according to Medicare claims data. The main predictor was functional impairment (level of difficulty or dependence in activities of daily living (ADLs)), determined from HRS interview preceding hospitalization. Multivariable linear regression was performed, adjusted for age, race, sex, income, net worth, and comorbidities, with clustering at the individual level to characterize the association between functional impairment and costs of postacute care.</p></div></div>
<div class="section" id="jgs14955-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Unadjusted mean Medicare costs for 1 year after discharge increased with severity of impairment in a dose-response fashion (<em>P</em> &lt; .001 for trend); 68% had no functional impairment ($25,931), 17% had difficulty with one ADL ($32,501), 7% had dependency in one ADL ($39,928), and 8% had dependency in two or more ADLs ($45,895). The most severely impaired participants cost 77% more than those with no impairment; adjusted analyses showed attenuated effect size (33% more) but no change in trend. Considering costs attributable to comorbidities, only three conditions were more expensive than severe functional impairment (lymphoma, metastatic cancer, paralysis).</p></div></div>
<div class="section" id="jgs14955-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Functional impairment is associated with greater Medicare costs for postacute care and may be an unmeasured but important marker of long-term costs that cuts across conditions.</p></div></div>
]]></content:encoded><description>

Objectives
To assess the effects of preadmission functional impairment on Medicare costs of postacute care up to 365 days after hospital discharge.


Design
Longitudinal cohort study.


Setting
Health and Retirement Study (HRS).


Participants
Nationally representative sample of 16,673 Medicare hospitalizations of 8,559 community-dwelling older adults from 2000 to 2012.


Measurements
The main outcome was total Medicare costs in the year after hospital discharge, assessed according to Medicare claims data. The main predictor was functional impairment (level of difficulty or dependence in activities of daily living (ADLs)), determined from HRS interview preceding hospitalization. Multivariable linear regression was performed, adjusted for age, race, sex, income, net worth, and comorbidities, with clustering at the individual level to characterize the association between functional impairment and costs of postacute care.


Results
Unadjusted mean Medicare costs for 1 year after discharge increased with severity of impairment in a dose-response fashion (P &lt; .001 for trend); 68% had no functional impairment ($25,931), 17% had difficulty with one ADL ($32,501), 7% had dependency in one ADL ($39,928), and 8% had dependency in two or more ADLs ($45,895). The most severely impaired participants cost 77% more than those with no impairment; adjusted analyses showed attenuated effect size (33% more) but no change in trend. Considering costs attributable to comorbidities, only three conditions were more expensive than severe functional impairment (lymphoma, metastatic cancer, paralysis).


Conclusion
Functional impairment is associated with greater Medicare costs for postacute care and may be an unmeasured but important marker of long-term costs that cuts across conditions.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14982" xmlns="http://purl.org/rss/1.0/"><title>Using Chief Complaint in Addition to Diagnosis Codes to Identify Falls in the Emergency Department</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14982</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Using Chief Complaint in Addition to Diagnosis Codes to Identify Falls in the Emergency Department</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Brian W. Patterson, Maureen A. Smith, Michael D. Repplinger, Michael S. Pulia, James E. Svenson, Michael K. Kim, Manish N. Shah</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-21T04:56:42.196635-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14982</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14982</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14982</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Geriatric Emergency Medicine</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14982-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To compare incidence of falls in an emergency department (ED) cohort using a traditional <em>International Classification of Diseases, Ninth Revision</em> (ICD-9) code–based scheme and an expanded definition that included chief complaint information and to examine the clinical characteristics of visits “missed” in the ICD-9-based scheme.</p></div></div>
<div class="section" id="jgs14982-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Retrospective electronic record review.</p></div></div>
<div class="section" id="jgs14982-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Academic medical center ED.</p></div></div>
<div class="section" id="jgs14982-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Individuals aged 65 and older seen in the ED between January 1, 2013, and September 30, 2015.</p></div></div>
<div class="section" id="jgs14982-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Two fall definitions were applied (individually and together) to the cohort: an ICD-9-based definition and a chief complaint definition. Admission rates and 30-day mortality (per encounter) were measured for each definition.</p></div></div>
<div class="section" id="jgs14982-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Twenty-three thousand eight hundred eighty older adult visits occurred during the study period. Using the most-inclusive definition (ICD-9 code or chief complaint indicating a fall), 4,363 visits (18%) were fall related. Of these visits, 3,506 (80%) met the ICD-9 definition for a fall-related visit, and 2,664 (61%) met the chief complaint definition. Of visits meeting the chief complaint definition, 857 (19.6%) were missed when applying the ICD-9 definition alone. Encounters missed using the ICD-9 definition were less likely to lead to an admission (42.9%, 95% confidence interval (CI) = 39.7–46.3%) than those identified (54.4%, 95% CI = 52.7–56.0%).</p></div></div>
<div class="section" id="jgs14982-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Identifying individuals in the ED who have fallen based on diagnosis codes underestimates the true burden of falls. Individuals missed according to the code-based definition were less likely to have been admitted than those who were captured. These findings call attention to the value of using chief complaint information to identify individuals who have fallen in the ED—for research, clinical care, or policy reasons.</p></div></div>
]]></content:encoded><description>

Objectives
To compare incidence of falls in an emergency department (ED) cohort using a traditional International Classification of Diseases, Ninth Revision (ICD-9) code–based scheme and an expanded definition that included chief complaint information and to examine the clinical characteristics of visits “missed” in the ICD-9-based scheme.


Design
Retrospective electronic record review.


Setting
Academic medical center ED.


Participants
Individuals aged 65 and older seen in the ED between January 1, 2013, and September 30, 2015.


Measurements
Two fall definitions were applied (individually and together) to the cohort: an ICD-9-based definition and a chief complaint definition. Admission rates and 30-day mortality (per encounter) were measured for each definition.


Results
Twenty-three thousand eight hundred eighty older adult visits occurred during the study period. Using the most-inclusive definition (ICD-9 code or chief complaint indicating a fall), 4,363 visits (18%) were fall related. Of these visits, 3,506 (80%) met the ICD-9 definition for a fall-related visit, and 2,664 (61%) met the chief complaint definition. Of visits meeting the chief complaint definition, 857 (19.6%) were missed when applying the ICD-9 definition alone. Encounters missed using the ICD-9 definition were less likely to lead to an admission (42.9%, 95% confidence interval (CI) = 39.7–46.3%) than those identified (54.4%, 95% CI = 52.7–56.0%).


Conclusion
Identifying individuals in the ED who have fallen based on diagnosis codes underestimates the true burden of falls. Individuals missed according to the code-based definition were less likely to have been admitted than those who were captured. These findings call attention to the value of using chief complaint information to identify individuals who have fallen in the ED—for research, clinical care, or policy reasons.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14973" xmlns="http://purl.org/rss/1.0/"><title>Reply To: Higher Intelligence and Later Maternal Age: Which Way Does the Causal Direction Go?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14973</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Reply To: Higher Intelligence and Later Maternal Age: Which Way Does the Causal Direction Go?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wendy J. Mack, Roksana Karim</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-21T01:45:25.232483-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14973</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14973</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14973</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14924" xmlns="http://purl.org/rss/1.0/"><title>Higher Intelligence and Later Maternal Age: Which Way Does the Causal Direction Go?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14924</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Higher Intelligence and Later Maternal Age: Which Way Does the Causal Direction Go?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Satoshi Kanazawa</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-20T02:25:21.76248-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14924</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14924</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14924</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14942" xmlns="http://purl.org/rss/1.0/"><title>Network for Investigation of Delirium across the U.S.: Advancing the Field of Delirium with a New Interdisciplinary Research Network</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14942</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Network for Investigation of Delirium across the U.S.: Advancing the Field of Delirium with a New Interdisciplinary Research Network</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Donna M. Fick, Andrew D. Auerbach, Michael S. Avidan, Jan Busby-Whitehead, E. Wesley Ely, Richard N. Jones, Edward R. Marcantonio, Dale M. Needham, Pratik Pandharipande, Thomas N. Robinson, Eva M. Schmitt, Thomas G. Travison, Sharon K. Inouye, </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-20T01:28:13.588676-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14942</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14942</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14942</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Editorial</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14958" xmlns="http://purl.org/rss/1.0/"><title>A Typology of Interprofessional Teamwork in Acute Geriatric Care: A Study in 55 units in Belgium</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14958</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A Typology of Interprofessional Teamwork in Acute Geriatric Care: A Study in 55 units in Belgium</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ruth D. Piers, Karen J. J. Versluys, Johan Devoghel, Sophie Lambrecht, André Vyt, Nele J. Van Den Noortgate</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-20T01:27:42.440458-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14958</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14958</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14958</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Brief Report</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14958-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To explore the quality of interprofessional teamwork in acute geriatric care and to build a model of team types.</p></div></div>
<div class="section" id="jgs14958-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Cross-sectional multicenter study.</p></div></div>
<div class="section" id="jgs14958-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Acute geriatric units in Belgium.</p></div></div>
<div class="section" id="jgs14958-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Team members of different professional backgrounds.</p></div></div>
<div class="section" id="jgs14958-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Perceptions of interprofessional teamwork among team members of 55 acute geriatric units in Belgium were measured using a survey covering collaborative practice and experience, managerial coaching and open team culture, shared reflection and decision-making, patient files facilitating teamwork, members’ belief in the power of teamwork, and members’ comfort in reporting incidents. Cluster analysis was used to determine types of interprofessional teamwork. Professions and clusters were compared using analysis of variance.</p></div></div>
<div class="section" id="jgs14958-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The overall response rate was 60%. Of the 890 respondents, 71% were nursing professionals, 20% other allied health professionals, 5% physicians, and 4% logistic and administrative staff. More than 70% of respondents scored highly on interprofessional teamwork competencies, consultation, experiences, meetings, management, and results. Fewer than 55% scored highly on items about shared reflection and decision-making, reporting incidents from a colleague, and patient files facilitating interprofessional teamwork. Nurses in this study rated shared reflection and decision-making lower than physicians on the same acute geriatric units (<em>P</em> &lt; .001). Using the mean score on each of the six areas, four clusters that differed significantly in all areas were identified using hierarchical cluster analysis and scree plot analysis (<em>P</em> &lt; .001).</p></div></div>
<div class="section" id="jgs14958-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Interprofessional teamwork in acute geriatric units is satisfactory, but shared reflection and decision-making needs improvement. Four types of interprofessional teamwork are identified and can be used to benchmark the teamwork of individual teams.</p></div></div>
]]></content:encoded><description>

Objectives
To explore the quality of interprofessional teamwork in acute geriatric care and to build a model of team types.


Design
Cross-sectional multicenter study.


Setting
Acute geriatric units in Belgium.


Participants
Team members of different professional backgrounds.


Measurements
Perceptions of interprofessional teamwork among team members of 55 acute geriatric units in Belgium were measured using a survey covering collaborative practice and experience, managerial coaching and open team culture, shared reflection and decision-making, patient files facilitating teamwork, members’ belief in the power of teamwork, and members’ comfort in reporting incidents. Cluster analysis was used to determine types of interprofessional teamwork. Professions and clusters were compared using analysis of variance.


Results
The overall response rate was 60%. Of the 890 respondents, 71% were nursing professionals, 20% other allied health professionals, 5% physicians, and 4% logistic and administrative staff. More than 70% of respondents scored highly on interprofessional teamwork competencies, consultation, experiences, meetings, management, and results. Fewer than 55% scored highly on items about shared reflection and decision-making, reporting incidents from a colleague, and patient files facilitating interprofessional teamwork. Nurses in this study rated shared reflection and decision-making lower than physicians on the same acute geriatric units (P &lt; .001). Using the mean score on each of the six areas, four clusters that differed significantly in all areas were identified using hierarchical cluster analysis and scree plot analysis (P &lt; .001).


Conclusion
Interprofessional teamwork in acute geriatric units is satisfactory, but shared reflection and decision-making needs improvement. Four types of interprofessional teamwork are identified and can be used to benchmark the teamwork of individual teams.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14985" xmlns="http://purl.org/rss/1.0/"><title>Discharge Against Medical Advice of Elderly Inpatients in the United States</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14985</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Discharge Against Medical Advice of Elderly Inpatients in the United States</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Carlijn Lelieveld, Rosanne Leipzig, Licia K. Gaber-Baylis, Madhu Mazumdar, Stavros G. Memtsoudis, Nicole Zubizarreta, Jashvant Poeran</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-19T02:40:27.803203-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14985</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14985</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14985</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Ethics, Public Policy &amp; Economics</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Discharge against medical advice (DAMA) is associated with greater risk of hospital readmission and higher morbidity, mortality, and costs, but with a rapidly increasing elderly inpatient population, there is a lack of national data on DAMA in this subgroup. The National Inpatient Sample (2003–2013 for trends, 2013 for multivariable analysis, n = 29,290,852) was used to describe trends in DAMA in elderly inpatients, to study diagnosis codes associated with admission, and to assess factors associated with DAMA using multivariable logistic regression. Odds ratios (ORs) and 95% confidence intervals (CIs) are reported for risk factors of interest. Although DAMA rates in individuals aged 65 and older were one fourth of those found in individuals aged 18 to 64, an increasing trend was found in both groups. From 2003 to 2013, rates increased in individuals aged 18 to 64 (from 1.44% to 1.78%) and in those aged 65 and older (from 0.37% to 0.42% (both <em>P</em> &lt; .001). In both age groups, individuals admitted for mental illness had the highest risk of DAMA. Factors associated with higher adjusted odds of DAMA were generally similar between age groups, although risk of DAMA was higher in elderly adults than in those aged 18 to 64 for blacks (OR 1.65, 95% CI 1.49–1.82 vs OR 1.16, 95% CI 1.12–1.20), Hispanics (OR 1.58, 95% CI 1.41–1.77 vs OR 0.83, 95% CI 0.79–0.87), and those in the lowest income quartile (OR 1.57, 95% CI 1.43–1.72 vs OR 1.12, 95% CI 1.08–1.17), suggesting that race/ethnicity and poverty are more pronounced as risk factors for DAMA in elderly inpatients.</p></div>
]]></content:encoded><description>
Discharge against medical advice (DAMA) is associated with greater risk of hospital readmission and higher morbidity, mortality, and costs, but with a rapidly increasing elderly inpatient population, there is a lack of national data on DAMA in this subgroup. The National Inpatient Sample (2003–2013 for trends, 2013 for multivariable analysis, n = 29,290,852) was used to describe trends in DAMA in elderly inpatients, to study diagnosis codes associated with admission, and to assess factors associated with DAMA using multivariable logistic regression. Odds ratios (ORs) and 95% confidence intervals (CIs) are reported for risk factors of interest. Although DAMA rates in individuals aged 65 and older were one fourth of those found in individuals aged 18 to 64, an increasing trend was found in both groups. From 2003 to 2013, rates increased in individuals aged 18 to 64 (from 1.44% to 1.78%) and in those aged 65 and older (from 0.37% to 0.42% (both P &lt; .001). In both age groups, individuals admitted for mental illness had the highest risk of DAMA. Factors associated with higher adjusted odds of DAMA were generally similar between age groups, although risk of DAMA was higher in elderly adults than in those aged 18 to 64 for blacks (OR 1.65, 95% CI 1.49–1.82 vs OR 1.16, 95% CI 1.12–1.20), Hispanics (OR 1.58, 95% CI 1.41–1.77 vs OR 0.83, 95% CI 0.79–0.87), and those in the lowest income quartile (OR 1.57, 95% CI 1.43–1.72 vs OR 1.12, 95% CI 1.08–1.17), suggesting that race/ethnicity and poverty are more pronounced as risk factors for DAMA in elderly inpatients.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14972" xmlns="http://purl.org/rss/1.0/"><title>Dietary Pattern Associated with Frailty: Results from Nutrition and Health Survey in Taiwan</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14972</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Dietary Pattern Associated with Frailty: Results from Nutrition and Health Survey in Taiwan</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yen-Li Lo, Yao-Te Hsieh, Li-Lin Hsu, Shao-Yuan Chuang, Hsing-Yi Chang, Chih-Cheng Hsu, Ching-Yu Chen, Wen-Harn Pan</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-12T01:01:02.51897-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14972</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14972</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14972</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14972-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To investigate whether dietary patterns are associated with frailty phenotypes in an elderly Taiwanese population.</p></div></div>
<div class="section" id="jgs14972-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Cross-sectional.</p></div></div>
<div class="section" id="jgs14972-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Nutrition and Health Survey in Taiwan (NAHSIT), 2014–2016.</p></div></div>
<div class="section" id="jgs14972-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Noninstitutionalized Taiwanese nationals aged 65 years and older enrolled in the NAHSIT (N = 923).</p></div></div>
<div class="section" id="jgs14972-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Dietary intake was assessed using a 79-item food-frequency questionnaire (FFQ). Presence of 5 frailty phenotypes was determined using modified Fried criteria and are summed into a frailty score. Using data from the NAHSIT (2014–15), reduced rank regression was used to find a dietary pattern that explained maximal degree of variation of the frailty scores. Logistic regression models were used to estimate the association between frailty and dietary pattern. The findings were validated with data from 2016.</p></div></div>
<div class="section" id="jgs14972-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The derived dietary pattern was characterized with a high consumption of fruit, nuts and seeds, tea, vegetables, whole grains, shellfish, milk, and fish. The prevalence of frailty was 7.8% and of prefrailty was 50.8%, defined using the modified Fried criteria. Using data from the NAHSIT (2014–15), the dietary pattern score showed an inverse dose-response relationship with prevalence of frailty and pre-frailty. Individuals in the second dietary pattern tertile were one-third as likely to be frail as those in the first tertile (adjusted odds ratio (aOR) = 0.32, 95% confidence interval (CI) = 0.12−0.85), and those in the third tertile were 4% as likely to be frail as those in the first tertile (aOR = 0.04, 95% CI = 0.01−0.18). The dietary pattern score estimated using FFQ data from the NAHSIT 2016 was also significantly and inversely associated with frailty.</p></div></div>
<div class="section" id="jgs14972-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Individuals with a dietary pattern with more phytonutrient-rich plant foods, tea, omega-3-rich deep-sea fish, and other protein-rich foods such as shellfish and milk had a reduced prevalence of frailty. Further research is necessary to confirm these findings and investigate whether related dietary interventions can reduce frailty in older adults.</p></div></div>
]]></content:encoded><description>

Objectives
To investigate whether dietary patterns are associated with frailty phenotypes in an elderly Taiwanese population.


Design
Cross-sectional.


Setting
Nutrition and Health Survey in Taiwan (NAHSIT), 2014–2016.


Participants
Noninstitutionalized Taiwanese nationals aged 65 years and older enrolled in the NAHSIT (N = 923).


Measurements
Dietary intake was assessed using a 79-item food-frequency questionnaire (FFQ). Presence of 5 frailty phenotypes was determined using modified Fried criteria and are summed into a frailty score. Using data from the NAHSIT (2014–15), reduced rank regression was used to find a dietary pattern that explained maximal degree of variation of the frailty scores. Logistic regression models were used to estimate the association between frailty and dietary pattern. The findings were validated with data from 2016.


Results
The derived dietary pattern was characterized with a high consumption of fruit, nuts and seeds, tea, vegetables, whole grains, shellfish, milk, and fish. The prevalence of frailty was 7.8% and of prefrailty was 50.8%, defined using the modified Fried criteria. Using data from the NAHSIT (2014–15), the dietary pattern score showed an inverse dose-response relationship with prevalence of frailty and pre-frailty. Individuals in the second dietary pattern tertile were one-third as likely to be frail as those in the first tertile (adjusted odds ratio (aOR) = 0.32, 95% confidence interval (CI) = 0.12−0.85), and those in the third tertile were 4% as likely to be frail as those in the first tertile (aOR = 0.04, 95% CI = 0.01−0.18). The dietary pattern score estimated using FFQ data from the NAHSIT 2016 was also significantly and inversely associated with frailty.


Conclusion
Individuals with a dietary pattern with more phytonutrient-rich plant foods, tea, omega-3-rich deep-sea fish, and other protein-rich foods such as shellfish and milk had a reduced prevalence of frailty. Further research is necessary to confirm these findings and investigate whether related dietary interventions can reduce frailty in older adults.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14970" xmlns="http://purl.org/rss/1.0/"><title>The Geriatrician Circa 2030</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14970</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The Geriatrician Circa 2030</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">John E. Morley</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-09T08:14:23.179152-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14970</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14970</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14970</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Perspectives of Geriatrics by Pioneers in Aging</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14944" xmlns="http://purl.org/rss/1.0/"><title>Periodontal Disease Associated with Higher Risk of Dementia: Population-Based Cohort Study in Taiwan</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14944</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Periodontal Disease Associated with Higher Risk of Dementia: Population-Based Cohort Study in Taiwan</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ya-Ling Lee, Hsiao-Yun Hu, Li-Ying Huang, Pesus Chou, Dachen Chu</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-09T07:50:28.003936-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14944</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14944</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14944</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14944-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To determine the magnitude and temporal aspect of the effect of poor dental health and periodontal disease (PD) on dementia.</p></div></div>
<div class="section" id="jgs14944-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Retrospective cohort study</p></div></div>
<div class="section" id="jgs14944-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Taiwan National Health Insurance Research Database.</p></div></div>
<div class="section" id="jgs14944-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Individuals with newly diagnosed PD (N = 182,747)</p></div></div>
<div class="section" id="jgs14944-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Participants were followed from January 1, 2000, to December 31, 2010. Participants were assigned to dental prophylaxis, intensive periodontal treatment, tooth extraction, or no treatment, according to International Classification of Diseases codes and PD treatment codes. The incidence rate of dementia of the groups was compared. The association between PD and dementia was analyzed using Cox regression, with adjustments for age, sex, monthly income, residential urbanicity, and comorbidities.</p></div></div>
<div class="section" id="jgs14944-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The incidence of dementia was significantly higher in the group with PD that did not receive treatment (0.76% per year) and in the group that had teeth extracted (0.57% per year) than in the group that underwent intensive PD treatment (0.35% per year) and the group that received dental prophylaxis (0.39% per year) (<em>P</em> &lt; .001). After adjusting for confounders, the Cox proportional hazards model revealed a higher risk of dementia in the group with PD who did not undergo treatment (hazard ratio (HR) = 1.14, 95% confidence interval (CI) = 1.04–1.24) and the group that had teeth extracted (HR = 1.10, 95% CI = 1.04–1.16) than in the group that received dental prophylaxis.</p></div></div>
<div class="section" id="jgs14944-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Subjects who had more severe PD or did not receive periodontal treatment were at greater risk of developing dementia.</p></div></div>
]]></content:encoded><description>

Objectives
To determine the magnitude and temporal aspect of the effect of poor dental health and periodontal disease (PD) on dementia.


Design
Retrospective cohort study


Setting
Taiwan National Health Insurance Research Database.


Participants
Individuals with newly diagnosed PD (N = 182,747)


Measurements
Participants were followed from January 1, 2000, to December 31, 2010. Participants were assigned to dental prophylaxis, intensive periodontal treatment, tooth extraction, or no treatment, according to International Classification of Diseases codes and PD treatment codes. The incidence rate of dementia of the groups was compared. The association between PD and dementia was analyzed using Cox regression, with adjustments for age, sex, monthly income, residential urbanicity, and comorbidities.


Results
The incidence of dementia was significantly higher in the group with PD that did not receive treatment (0.76% per year) and in the group that had teeth extracted (0.57% per year) than in the group that underwent intensive PD treatment (0.35% per year) and the group that received dental prophylaxis (0.39% per year) (P &lt; .001). After adjusting for confounders, the Cox proportional hazards model revealed a higher risk of dementia in the group with PD who did not undergo treatment (hazard ratio (HR) = 1.14, 95% confidence interval (CI) = 1.04–1.24) and the group that had teeth extracted (HR = 1.10, 95% CI = 1.04–1.16) than in the group that received dental prophylaxis.


Conclusion
Subjects who had more severe PD or did not receive periodontal treatment were at greater risk of developing dementia.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14964" xmlns="http://purl.org/rss/1.0/"><title>Functional Impairment and Risk of Venous Thrombosis in Older Adults</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14964</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Functional Impairment and Risk of Venous Thrombosis in Older Adults</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marissa J. Engbers, Jeanet W. Blom, Mary Cushman, Frits R. Rosendaal, Astrid Hylckama Vlieg</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-09T07:50:20.86722-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14964</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14964</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14964</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14964-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To determine the role of age-specific risk factors for thrombosis in older age, such as functional impairment.</p></div></div>
<div class="section" id="jgs14964-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Case-control study.</p></div></div>
<div class="section" id="jgs14964-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>The Age and Thrombosis—Acquired and Genetic risk factors in the Elderly Study, a two-center study conducted in the Netherlands and the United States from 2008 to 2011.</p></div></div>
<div class="section" id="jgs14964-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Individuals aged 70 and older with a first-time deep venous thrombosis in the leg or pulmonary embolism (n = 401) and controls aged 70 and older (n = 431) without a history of thrombosis. Exclusion criteria were active malignancy and severe cognitive disorders.</p></div></div>
<div class="section" id="jgs14964-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>The thrombotic risk associated with functional impairment, defined as impairment in two or more activities of daily living (ADLs), impaired mobility (inability to walk outside), sedentary lifestyle (≥20 h/d sleeping or sitting), and low handgrip strength (&lt;15th percentile), was assessed. Odds ratios (ORs) adjusted for age, sex, and study center with 95% confidence intervals (95% CI) and population attributable risks (PAR) were calculated.</p></div></div>
<div class="section" id="jgs14964-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Risk of venous thrombosis was 2.9 times greater (OR = 2.9, 95% CI = 1.6–5.3) in individuals with impairment in ADLs, three times as great (OR = 3.0, 95% CI = 1.9–4.7) in those with impaired mobility, four times as great (OR = 4.0, 95% CI = 2.5–6.3) in those with a sedentary life style, and 2.3 times as great (OR = 2.3, 95% CI = 1.5–3.4) in those with weak handgrip strength. PARs were 8% for ADL disability, 13% for inability to walk outside for 15 minutes, 29% for sedentary lifestyle, and 13% for weak hand grip strength.</p></div></div>
<div class="section" id="jgs14964-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>In individuals aged 70 and older, functional impairments are a major risk factor for venous thrombosis. These findings may help providers caring for older people be more aware of venous thrombosis risk.</p></div></div>
]]></content:encoded><description>

Objectives
To determine the role of age-specific risk factors for thrombosis in older age, such as functional impairment.


Design
Case-control study.


Setting
The Age and Thrombosis—Acquired and Genetic risk factors in the Elderly Study, a two-center study conducted in the Netherlands and the United States from 2008 to 2011.


Participants
Individuals aged 70 and older with a first-time deep venous thrombosis in the leg or pulmonary embolism (n = 401) and controls aged 70 and older (n = 431) without a history of thrombosis. Exclusion criteria were active malignancy and severe cognitive disorders.


Measurements
The thrombotic risk associated with functional impairment, defined as impairment in two or more activities of daily living (ADLs), impaired mobility (inability to walk outside), sedentary lifestyle (≥20 h/d sleeping or sitting), and low handgrip strength (&lt;15th percentile), was assessed. Odds ratios (ORs) adjusted for age, sex, and study center with 95% confidence intervals (95% CI) and population attributable risks (PAR) were calculated.


Results
Risk of venous thrombosis was 2.9 times greater (OR = 2.9, 95% CI = 1.6–5.3) in individuals with impairment in ADLs, three times as great (OR = 3.0, 95% CI = 1.9–4.7) in those with impaired mobility, four times as great (OR = 4.0, 95% CI = 2.5–6.3) in those with a sedentary life style, and 2.3 times as great (OR = 2.3, 95% CI = 1.5–3.4) in those with weak handgrip strength. PARs were 8% for ADL disability, 13% for inability to walk outside for 15 minutes, 29% for sedentary lifestyle, and 13% for weak hand grip strength.


Conclusion
In individuals aged 70 and older, functional impairments are a major risk factor for venous thrombosis. These findings may help providers caring for older people be more aware of venous thrombosis risk.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14956" xmlns="http://purl.org/rss/1.0/"><title>Proton Pump Inhibitors and Risk of Mild Cognitive Impairment and Dementia</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14956</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Proton Pump Inhibitors and Risk of Mild Cognitive Impairment and Dementia</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Felicia C. Goldstein, Kyle Steenland, Liping Zhao, Whitney Wharton, Allan I. Levey, Ihab Hajjar</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-07T04:55:23.084485-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14956</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14956</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14956</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14956-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To examine the risk associated with the use of proton pump inhibitors (PPIs) of conversion to mild cognitive impairment (MCI), dementia, and specifically Alzheimer's disease (AD).</p></div></div>
<div class="section" id="jgs14956-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Observational, longitudinal study.</p></div></div>
<div class="section" id="jgs14956-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Tertiary academic Alzheimer's Disease Centers funded by the National Institute on Aging.</p></div></div>
<div class="section" id="jgs14956-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Research volunteers aged 50 and older with two to six annual visits; 884 were taking PPIs at every visit, 1,925 took PPIs intermittently, and 7,677 never reported taking PPIs. All had baseline normal cognition or MCI.</p></div></div>
<div class="section" id="jgs14956-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Multivariable Cox regression analyses evaluated the association between PPI use and annual conversion of baseline normal cognition to MCI or dementia or annual conversion of baseline MCI to dementia, controlling for demographic characteristics, vascular comorbidities, mood, and use of anticholinergics and histamine-2 receptor antagonists.</p></div></div>
<div class="section" id="jgs14956-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Continuous (always vs never) PPI use was associated with lower risk of decline in cognitive function (hazard ratio (HR) = 0.78, 95% confidence interval (CI) =0.66–0.93, <em>P</em> = .005) and lower risk of conversion to MCI or AD (HR = 0.82, 95% CI = 0.69–0.98, <em>P</em> = .03). Intermittent use was also associated with lower risk of decline in cognitive function (HR = 0.84, 95% CI = 0.76–0.93, <em>P</em> = .001) and risk of conversion to MCI or AD (HR = 0.82, 95% CI = 0.74–0.91, <em>P</em> = .001). This lower risk was found for persons with normal cognition or MCI.</p></div></div>
<div class="section" id="jgs14956-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Proton pump inhibitors were not associated with greater risk of dementia or of AD, in contrast to recent reports. Study limitations include reliance on self-reported PPI use and lack of dispensing data. Prospective studies are needed to confirm these results to guide empirically based clinical treatment recommendations.</p></div></div>
]]></content:encoded><description>

Objectives
To examine the risk associated with the use of proton pump inhibitors (PPIs) of conversion to mild cognitive impairment (MCI), dementia, and specifically Alzheimer's disease (AD).


Design
Observational, longitudinal study.


Setting
Tertiary academic Alzheimer's Disease Centers funded by the National Institute on Aging.


Participants
Research volunteers aged 50 and older with two to six annual visits; 884 were taking PPIs at every visit, 1,925 took PPIs intermittently, and 7,677 never reported taking PPIs. All had baseline normal cognition or MCI.


Measurements
Multivariable Cox regression analyses evaluated the association between PPI use and annual conversion of baseline normal cognition to MCI or dementia or annual conversion of baseline MCI to dementia, controlling for demographic characteristics, vascular comorbidities, mood, and use of anticholinergics and histamine-2 receptor antagonists.


Results
Continuous (always vs never) PPI use was associated with lower risk of decline in cognitive function (hazard ratio (HR) = 0.78, 95% confidence interval (CI) =0.66–0.93, P = .005) and lower risk of conversion to MCI or AD (HR = 0.82, 95% CI = 0.69–0.98, P = .03). Intermittent use was also associated with lower risk of decline in cognitive function (HR = 0.84, 95% CI = 0.76–0.93, P = .001) and risk of conversion to MCI or AD (HR = 0.82, 95% CI = 0.74–0.91, P = .001). This lower risk was found for persons with normal cognition or MCI.


Conclusion
Proton pump inhibitors were not associated with greater risk of dementia or of AD, in contrast to recent reports. Study limitations include reliance on self-reported PPI use and lack of dispensing data. Prospective studies are needed to confirm these results to guide empirically based clinical treatment recommendations.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14976" xmlns="http://purl.org/rss/1.0/"><title>Reply to: Estimating the Full Value of the High-Dose Influenza Vaccine</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14976</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Reply to: Estimating the Full Value of the High-Dose Influenza Vaccine</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jonathan M. Raviotta, Kenneth J. Smith, Jay DePasse, Shawn T. Brown, Eunha Shim, Mary Patricia Nowalk, Richard K. Zimmerman</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-06T07:30:27.734767-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14976</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14976</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14976</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14950" xmlns="http://purl.org/rss/1.0/"><title>Estimating the Full Value of High-Dose Influenza Vaccine</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14950</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Estimating the Full Value of High-Dose Influenza Vaccine</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Brennan Ertmer, Ayman Chit</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-06T07:30:25.577044-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14950</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14950</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14950</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14978" xmlns="http://purl.org/rss/1.0/"><title>Male Centenarians: How and Why Are They Different from Their Female Counterparts?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14978</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Male Centenarians: How and Why Are They Different from Their Female Counterparts?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Thomas T. Perls</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-06T07:30:23.233386-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14978</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14978</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14978</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Editorial</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14979" xmlns="http://purl.org/rss/1.0/"><title>The Geriatrics 5M's: A new way of communicating what we do</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14979</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The Geriatrics 5M's: A new way of communicating what we do</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mary Tinetti, Allen Huang, Frank Molnar</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-06T07:30:20.211523-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14979</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14979</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14979</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14974" xmlns="http://purl.org/rss/1.0/"><title>Seventeen Hours</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14974</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Seventeen Hours</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Alyson E. Dobracki</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-06T07:25:19.57593-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14974</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14974</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14974</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Old Lives Tale</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14935" xmlns="http://purl.org/rss/1.0/"><title>Influence of Hospital Type on Outcomes of Individuals Aged 80 and Older with Stroke Treated Using Intravenous Thrombolysis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14935</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Influence of Hospital Type on Outcomes of Individuals Aged 80 and Older with Stroke Treated Using Intravenous Thrombolysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Francisco Purroy, Ana Vena, David Cánovas, Pere Cardona, Dolores Cocho, Elisa Cuadrado-Godia, Angel Chamorro, Antonio Dávalos, Moisés Garcés, Meritxell Gomis, Jerzy Krupinski, Ernest Palomeras, Marc Ribó, Jaume Roquer, Marta Rubiera, Jordi Sanahuja, Júlia Saura, Joaquín Serena, Xavier Ustrell, Martha Vargas, Ikram Benabdelhak, Sonia Abilleira, Miquel Gallofré, </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-02T09:15:25.416412-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14935</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14935</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14935</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14935-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>The aim of the study was to confirm the safety and effectiveness of using intravenous thrombolysis (IVT) with individuals aged 80 and older in routine practice in different hospital settings.</p></div></div>
<div class="section" id="jgs14935-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Observasional registry.</p></div></div>
<div class="section" id="jgs14935-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Prospective multicenter population-based registry of acute stroke patients treated with reperfusion therapies in Catalonia, Spain (Sistema Online d'Informació de l'Ictus Agut).</p></div></div>
<div class="section" id="jgs14935-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Individuals treated only with IVT (N = 3,231; 1,189 (36.8%) aged ≥80).</p></div></div>
<div class="section" id="jgs14935-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Symptomatic intracranial hemorrhage, mortality, and favorable outcome (modified Rankin Scale (mRS) score = 0–2) at 3 months were evaluated according to hospital characteristics. Treating hospitals were classified in three categories: comprehensive stroke centers (CSCs), primary stroke centers (PSCs), and community hospitals operating a telestroke system (TS). First individuals aged 80 and older were compared with those younger than 80, and then participants aged 80 and older were focused on.</p></div></div>
<div class="section" id="jgs14935-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Participants aged 80 and older had significantly higher baseline National Institute of Health Stroke Scale (NIHSS) scores, longer onset to treatment times, and worse outcomes than younger participants. For participants aged 80 and older, 90-day mortality was 23.2%, with 38.7% having favorable outcomes at 3 months. Symptomatic intracranial hemorrhage (SICH; Safe Implementation of Thrombolysis in Stroke-MOnitoring STudy definition) was observed in 4.7% of subjects. None of the risk factors differed significantly between participants treated in different types of hospitals. Basal stroke severity measured according to NIHSS score was not significantly different either. The three different types of hospitals achieved similar outcomes, although the TS and PSC hospitals had significantly higher proportions of SICH (6.3% and 6.3%, respectively) than the CSC (3.2%).</p></div></div>
<div class="section" id="jgs14935-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Older adults with acute stroke treated with IVT had similar outcomes regardless of hospital characteristics.</p></div></div>
]]></content:encoded><description>

Objectives
The aim of the study was to confirm the safety and effectiveness of using intravenous thrombolysis (IVT) with individuals aged 80 and older in routine practice in different hospital settings.


Design
Observasional registry.


Setting
Prospective multicenter population-based registry of acute stroke patients treated with reperfusion therapies in Catalonia, Spain (Sistema Online d'Informació de l'Ictus Agut).


Participants
Individuals treated only with IVT (N = 3,231; 1,189 (36.8%) aged ≥80).


Measurements
Symptomatic intracranial hemorrhage, mortality, and favorable outcome (modified Rankin Scale (mRS) score = 0–2) at 3 months were evaluated according to hospital characteristics. Treating hospitals were classified in three categories: comprehensive stroke centers (CSCs), primary stroke centers (PSCs), and community hospitals operating a telestroke system (TS). First individuals aged 80 and older were compared with those younger than 80, and then participants aged 80 and older were focused on.


Results
Participants aged 80 and older had significantly higher baseline National Institute of Health Stroke Scale (NIHSS) scores, longer onset to treatment times, and worse outcomes than younger participants. For participants aged 80 and older, 90-day mortality was 23.2%, with 38.7% having favorable outcomes at 3 months. Symptomatic intracranial hemorrhage (SICH; Safe Implementation of Thrombolysis in Stroke-MOnitoring STudy definition) was observed in 4.7% of subjects. None of the risk factors differed significantly between participants treated in different types of hospitals. Basal stroke severity measured according to NIHSS score was not significantly different either. The three different types of hospitals achieved similar outcomes, although the TS and PSC hospitals had significantly higher proportions of SICH (6.3% and 6.3%, respectively) than the CSC (3.2%).


Conclusion
Older adults with acute stroke treated with IVT had similar outcomes regardless of hospital characteristics.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14959" xmlns="http://purl.org/rss/1.0/"><title>Hemoglobin Concentration Influences N-Terminal Pro B-Type Natriuretic Peptide Levels in Hospitalized Older Adults with and without Heart Failure</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14959</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Hemoglobin Concentration Influences N-Terminal Pro B-Type Natriuretic Peptide Levels in Hospitalized Older Adults with and without Heart Failure</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Diana Lelli, Raffaele Antonelli Incalzi, Claudio Pedone</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-05-29T08:50:26.819715-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14959</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14959</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14959</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14959-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To investigate the relationship between hemoglobin and N-terminal pro B-type natriuretic peptide (NT-proBNP) concentration in hospitalized older adults with or without a diagnosis of heart failure (HF).</p></div></div>
<div class="section" id="jgs14959-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Cross-sectional study based on retrospective hospital records review.</p></div></div>
<div class="section" id="jgs14959-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Geriatric acute care ward.</p></div></div>
<div class="section" id="jgs14959-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Individuals aged 65 and older (N = 226; mean age 81.1), with (n = 104) and without (n = 122) a diagnosis of HF.</p></div></div>
<div class="section" id="jgs14959-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Information was collected on demographic characteristics, comorbidities, and laboratory and echocardiographic data. The relationship between hemoglobin and NT-proBNP was evaluated using linear regression models adjusted for potential confounders.</p></div></div>
<div class="section" id="jgs14959-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>A negative association was found between NT-proBNP and hemoglobin (β<em> </em>= −0.226, <em>P</em> &lt; .001). The regression coefficient was −0.114 (<em>P</em> = .04) in the subsample with HF and −0.191 (<em>P</em> &lt; .001) in the subsample without HF. After adjustment for potential confounders, the inverse association between hemoglobin and NT-proBNP was confirmed in the whole sample (β<em> </em>= −0.182, <em>P</em> &lt; .001), in those with HF (β<em> </em>= −0.136, <em>P</em> = .007), and in those without HF (β<em> </em>= −0.165, <em>P</em> = .003).</p></div></div>
<div class="section" id="jgs14959-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Hemoglobin concentration should be taken into account in the interpretation of NT-proBNP in hospitalized older adults, especially those without HF.</p></div></div>
]]></content:encoded><description>

Objectives
To investigate the relationship between hemoglobin and N-terminal pro B-type natriuretic peptide (NT-proBNP) concentration in hospitalized older adults with or without a diagnosis of heart failure (HF).


Design
Cross-sectional study based on retrospective hospital records review.


Setting
Geriatric acute care ward.


Participants
Individuals aged 65 and older (N = 226; mean age 81.1), with (n = 104) and without (n = 122) a diagnosis of HF.


Measurements
Information was collected on demographic characteristics, comorbidities, and laboratory and echocardiographic data. The relationship between hemoglobin and NT-proBNP was evaluated using linear regression models adjusted for potential confounders.


Results
A negative association was found between NT-proBNP and hemoglobin (β = −0.226, P &lt; .001). The regression coefficient was −0.114 (P = .04) in the subsample with HF and −0.191 (P &lt; .001) in the subsample without HF. After adjustment for potential confounders, the inverse association between hemoglobin and NT-proBNP was confirmed in the whole sample (β = −0.182, P &lt; .001), in those with HF (β = −0.136, P = .007), and in those without HF (β = −0.165, P = .003).


Conclusion
Hemoglobin concentration should be taken into account in the interpretation of NT-proBNP in hospitalized older adults, especially those without HF.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14937" xmlns="http://purl.org/rss/1.0/"><title>Seeking Value in Healthcare: The Importance of Generalists as Primary Care Physicians</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14937</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Seeking Value in Healthcare: The Importance of Generalists as Primary Care Physicians</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Samuel T. Edwards, Bruce E. Landon</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-05-29T01:01:01.965192-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14937</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14937</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14937</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Editorial</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14911" xmlns="http://purl.org/rss/1.0/"><title>Long-Term Oral Bisphosphonate Therapy and Fractures in Older Women: The Women's Health Initiative</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14911</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Long-Term Oral Bisphosphonate Therapy and Fractures in Older Women: The Women's Health Initiative</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rebecca L. Drieling, Andrea Z. LaCroix, Shirley A. A. Beresford, Denise M. Boudreau, Charles Kooperberg, Rowan T. Chlebowski, Marcia G. Ko, Susan R. Heckbert</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-05-29T00:05:33.512875-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14911</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14911</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14911</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14911-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To examine the association between long-term bisphosphonate use and fracture in older women at high risk of fracture.</p></div></div>
<div class="section" id="jgs14911-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Retrospective cohort.</p></div></div>
<div class="section" id="jgs14911-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Women's Health Initiative.</p></div></div>
<div class="section" id="jgs14911-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Older women who reported at least 2 years of bisphosphonate use in 2008–09 (N = 5,120).</p></div></div>
<div class="section" id="jgs14911-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Exposure data were from a current medications inventory. Outcomes (hip, clinical vertebral, wrist or forearm, any clinical fracture) were ascertained annually. Using multivariate Cox proportional hazards models, the association between duration of bisphosphonate use (3–5, 6–9, 10–13 years) and fracture was estimated, using 2 years as the referent group.</p></div></div>
<div class="section" id="jgs14911-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>On average participants were 80 years old and were followed for 3.7 ± 1.2 years. There were 127 hip, 159 wrist or forearm, 235 clinical vertebral, and 1,313 clinical fractures. In multivariate-adjusted analysis, 10 to 13 years of bisphosphonate use was associated with higher risk of any clinical fracture than 2 years of use (hazard ratio (HR) = 1.29, 95% confidence interval (CI) = 1.07–1.57). This association persisted in analyses limited to women with a prior fracture (HR = 1.30, 95% CI = 1.01–1.67) and women with no history of cancer (HR = 1.36, 95% CI = 1.10–1.68). The association of 10 to 13 years of use, compared with 2 years of use, was not statistically significant for hip (HR = 1.66, 95% CI = 0.81–3.40), clinical vertebral (HR = 1.65, 95% CI = 0.99–2.76), or wrist fracture (HR = 1.16, 95% CI = 0.67–2.00).</p></div></div>
<div class="section" id="jgs14911-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>In older women at high risk of fracture, 10 to 13 years of bisphosphonate use was associated with higher risk of any clinical fracture than 2 years of use. These results add to concerns about the benefit of very long-term bisphosphonate use.</p></div></div>
]]></content:encoded><description>

Objectives
To examine the association between long-term bisphosphonate use and fracture in older women at high risk of fracture.


Design
Retrospective cohort.


Setting
Women's Health Initiative.


Participants
Older women who reported at least 2 years of bisphosphonate use in 2008–09 (N = 5,120).


Measurements
Exposure data were from a current medications inventory. Outcomes (hip, clinical vertebral, wrist or forearm, any clinical fracture) were ascertained annually. Using multivariate Cox proportional hazards models, the association between duration of bisphosphonate use (3–5, 6–9, 10–13 years) and fracture was estimated, using 2 years as the referent group.


Results
On average participants were 80 years old and were followed for 3.7 ± 1.2 years. There were 127 hip, 159 wrist or forearm, 235 clinical vertebral, and 1,313 clinical fractures. In multivariate-adjusted analysis, 10 to 13 years of bisphosphonate use was associated with higher risk of any clinical fracture than 2 years of use (hazard ratio (HR) = 1.29, 95% confidence interval (CI) = 1.07–1.57). This association persisted in analyses limited to women with a prior fracture (HR = 1.30, 95% CI = 1.01–1.67) and women with no history of cancer (HR = 1.36, 95% CI = 1.10–1.68). The association of 10 to 13 years of use, compared with 2 years of use, was not statistically significant for hip (HR = 1.66, 95% CI = 0.81–3.40), clinical vertebral (HR = 1.65, 95% CI = 0.99–2.76), or wrist fracture (HR = 1.16, 95% CI = 0.67–2.00).


Conclusion
In older women at high risk of fracture, 10 to 13 years of bisphosphonate use was associated with higher risk of any clinical fracture than 2 years of use. These results add to concerns about the benefit of very long-term bisphosphonate use.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14948" xmlns="http://purl.org/rss/1.0/"><title>Have We Learned How to Use Bisphosphonates Yet?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14948</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Have We Learned How to Use Bisphosphonates Yet?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kenneth W. Lyles</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-05-29T00:05:25.680034-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14948</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14948</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14948</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Editorial</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14913" xmlns="http://purl.org/rss/1.0/"><title>High C-Reactive Protein Predicts Delirium Incidence, Duration, and Feature Severity After Major Noncardiac Surgery</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14913</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">High C-Reactive Protein Predicts Delirium Incidence, Duration, and Feature Severity After Major Noncardiac Surgery</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sarinnapha M. Vasunilashorn, Simon T. Dillon, Sharon K. Inouye, Long H. Ngo, Tamara G. Fong, Richard N. Jones, Thomas G. Travison, Eva M. Schmitt, David C. Alsop, Steven D. Freedman, Steven E. Arnold, Eran D. Metzger, Towia A. Libermann, Edward R. Marcantonio</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-05-26T14:40:30.18597-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14913</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14913</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14913</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14913-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To examine associations between the inflammatory marker C-reactive protein (CRP) measured preoperatively and on postoperative day 2 (POD2) and delirium incidence, duration, and feature severity.</p></div></div>
<div class="section" id="jgs14913-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Prospective cohort study.</p></div></div>
<div class="section" id="jgs14913-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Two academic medical centers.</p></div></div>
<div class="section" id="jgs14913-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Adults aged 70 and older undergoing major noncardiac surgery (N = 560).</p></div></div>
<div class="section" id="jgs14913-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Plasma CRP was measured using enzyme-linked immunosorbent assay. Delirium was assessed from Confusion Assessment Method (CAM) interviews and chart review. Delirium duration was measured according to number of hospital days with delirium. Delirium feature severity was defined as the sum of CAM-Severity (CAM-S) scores on all postoperative hospital days. Generalized linear models were used to examine independent associations between CRP (preoperatively and POD2 separately) and delirium incidence, duration, and feature severity; prolonged hospital length of stay (LOS, &gt;5 days); and discharge disposition.</p></div></div>
<div class="section" id="jgs14913-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Postoperative delirium occurred in 24% of participants, 12% had 2 or more delirium days, and the mean ± standard deviation sum CAM-S was 9.3 ± 11.4. After adjusting for age, sex, surgery type, anesthesia route, medical comorbidities, and postoperative infectious complications, participants with preoperative CRP of 3 mg/L or greater had a risk of delirium that was 1.5 times as great (95% confidence interval (CI) = 1.1–2.1) as that of those with CRP less than 3 mg/L, 0.4 more delirium days (<em>P</em> &lt; .001), more-severe delirium (3.6 CAM-S points higher, <em>P</em> &lt; .001), and a risk of prolonged LOS that was 1.4 times as great (95% CI = 1.1–1.8). Using POD2 CRP, participants in the highest quartile (≥235.73 mg/L) were 1.5 times as likely to develop delirium (95% CI = 1.0–2.4) as those in the lowest quartile (≤127.53 mg/L), had 0.2 more delirium days (<em>P</em> &lt; .05), and had more severe delirium (4.5 CAM-S points higher, <em>P</em> &lt; .001).</p></div></div>
<div class="section" id="jgs14913-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>High preoperative and POD2 CRP were independently associated with delirium incidence, duration, and feature severity. CRP may be useful to identify individuals who are at risk of developing delirium.</p></div></div>
]]></content:encoded><description>

Objectives
To examine associations between the inflammatory marker C-reactive protein (CRP) measured preoperatively and on postoperative day 2 (POD2) and delirium incidence, duration, and feature severity.


Design
Prospective cohort study.


Setting
Two academic medical centers.


Participants
Adults aged 70 and older undergoing major noncardiac surgery (N = 560).


Measurements
Plasma CRP was measured using enzyme-linked immunosorbent assay. Delirium was assessed from Confusion Assessment Method (CAM) interviews and chart review. Delirium duration was measured according to number of hospital days with delirium. Delirium feature severity was defined as the sum of CAM-Severity (CAM-S) scores on all postoperative hospital days. Generalized linear models were used to examine independent associations between CRP (preoperatively and POD2 separately) and delirium incidence, duration, and feature severity; prolonged hospital length of stay (LOS, &gt;5 days); and discharge disposition.


Results
Postoperative delirium occurred in 24% of participants, 12% had 2 or more delirium days, and the mean ± standard deviation sum CAM-S was 9.3 ± 11.4. After adjusting for age, sex, surgery type, anesthesia route, medical comorbidities, and postoperative infectious complications, participants with preoperative CRP of 3 mg/L or greater had a risk of delirium that was 1.5 times as great (95% confidence interval (CI) = 1.1–2.1) as that of those with CRP less than 3 mg/L, 0.4 more delirium days (P &lt; .001), more-severe delirium (3.6 CAM-S points higher, P &lt; .001), and a risk of prolonged LOS that was 1.4 times as great (95% CI = 1.1–1.8). Using POD2 CRP, participants in the highest quartile (≥235.73 mg/L) were 1.5 times as likely to develop delirium (95% CI = 1.0–2.4) as those in the lowest quartile (≤127.53 mg/L), had 0.2 more delirium days (P &lt; .05), and had more severe delirium (4.5 CAM-S points higher, P &lt; .001).


Conclusion
High preoperative and POD2 CRP were independently associated with delirium incidence, duration, and feature severity. CRP may be useful to identify individuals who are at risk of developing delirium.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14936" xmlns="http://purl.org/rss/1.0/"><title>Bone Turnover with Venlafaxine Treatment in Older Adults with Depression</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14936</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Bone Turnover with Venlafaxine Treatment in Older Adults with Depression</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kerri S. Rawson, David Dixon, Roberto Civitelli, Tim R. Peterson, Benoit H. Mulsant, Charles F. Reynolds, Eric J. Lenze</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-05-26T14:40:27.483137-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14936</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14936</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14936</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Brief Report</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14936-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>Epidemiologic data suggest older adults receiving serotonergic antidepressants may have accelerated bone loss. We examined bone turnover marker changes and patient-level variables associated with these changes in older adults receiving protocolized antidepressant treatment.</p></div></div>
<div class="section" id="jgs14936-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Open-label, protocolized treatment study.</p></div></div>
<div class="section" id="jgs14936-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Medical centers in Pittsburgh, St Louis, and Toronto.</p></div></div>
<div class="section" id="jgs14936-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Older adults with major depression (N = 168).</p></div></div>
<div class="section" id="jgs14936-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Serum levels of the bone resorption marker C-terminal cross-linking telopeptide of type 1 collagen (CTX) and the bone formation marker procollagen type 1 N propeptide (P1NP) were assayed before and after 12 weeks of treatment with venlafaxine. Whether CTX and P1NP changes were associated with depression remission and duration of depression and genetic polymorphisms in the serotonin transporter (5HTTLPR) and 1B receptor (HTR1B) were also examined.</p></div></div>
<div class="section" id="jgs14936-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>CTX increased and P1NP decreased during venlafaxine treatment, a profile consistent with accelerated bone loss. Two individual-level clinical variables were correlated with bone turnover; participants whose depression did not go into remission had higher CTX levels, and those with chronic depression had lower P1NP levels. HTR1B genotype predicted P1NP change, whereas 5HTTLPR genotype was unrelated to either biomarker.</p></div></div>
<div class="section" id="jgs14936-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Bone turnover markers change with antidepressant treatment in a pattern that suggests accelerated bone loss, although the clinical significance of these changes is unclear. These data are preliminary and argue for a larger, controlled study to confirm whether antidepressants are harmful to bone metabolism and whether certain individuals might be at increased risk.</p></div></div>
]]></content:encoded><description>

Objectives
Epidemiologic data suggest older adults receiving serotonergic antidepressants may have accelerated bone loss. We examined bone turnover marker changes and patient-level variables associated with these changes in older adults receiving protocolized antidepressant treatment.


Design
Open-label, protocolized treatment study.


Setting
Medical centers in Pittsburgh, St Louis, and Toronto.


Participants
Older adults with major depression (N = 168).


Measurements
Serum levels of the bone resorption marker C-terminal cross-linking telopeptide of type 1 collagen (CTX) and the bone formation marker procollagen type 1 N propeptide (P1NP) were assayed before and after 12 weeks of treatment with venlafaxine. Whether CTX and P1NP changes were associated with depression remission and duration of depression and genetic polymorphisms in the serotonin transporter (5HTTLPR) and 1B receptor (HTR1B) were also examined.


Results
CTX increased and P1NP decreased during venlafaxine treatment, a profile consistent with accelerated bone loss. Two individual-level clinical variables were correlated with bone turnover; participants whose depression did not go into remission had higher CTX levels, and those with chronic depression had lower P1NP levels. HTR1B genotype predicted P1NP change, whereas 5HTTLPR genotype was unrelated to either biomarker.


Conclusion
Bone turnover markers change with antidepressant treatment in a pattern that suggests accelerated bone loss, although the clinical significance of these changes is unclear. These data are preliminary and argue for a larger, controlled study to confirm whether antidepressants are harmful to bone metabolism and whether certain individuals might be at increased risk.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14625" xmlns="http://purl.org/rss/1.0/"><title>Cover</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14625</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Cover</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-12T06:32:30.490803-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14625</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14625</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14625</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Cover</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">C1</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">C1</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14627" xmlns="http://purl.org/rss/1.0/"><title>Issue Information</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14627</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Issue Information</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-12T06:32:23.29008-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14627</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14627</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14627</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Issue Information</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1373</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1385</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14941" xmlns="http://purl.org/rss/1.0/"><title>When It Comes to Older Adults, Language Matters: Journal of the American Geriatrics Society Adopts Modified American Medical Association Style</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14941</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">When It Comes to Older Adults, Language Matters: Journal of the American Geriatrics Society Adopts Modified American Medical Association Style</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nancy E. Lundebjerg, Daniel E. Trucil, Emily C. Hammond, William B. Applegate</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-06-01T00:01:02.387942-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14941</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14941</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14941</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Editorial</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1386</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1388</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14842" xmlns="http://purl.org/rss/1.0/"><title>Evolution of Geriatric Medicine: Midcareer Faculty Continuing the Dialogue</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14842</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Evolution of Geriatric Medicine: Midcareer Faculty Continuing the Dialogue</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lona Mody, Malaz Boustani, Ursula K Braun, Catherine Sarkisian</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-04-10T09:35:24.804363-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14842</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14842</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14842</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Editorial</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1389</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1391</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14881" xmlns="http://purl.org/rss/1.0/"><title>Finding the Distribution Channels for Effective Transitional Care Services</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14881</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Finding the Distribution Channels for Effective Transitional Care Services</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Babar A. Khan, Catherine A. Alder, Malaz A. Boustani</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-29T12:18:04.592255-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14881</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14881</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14881</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Editorial</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1392</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1393</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14916" xmlns="http://purl.org/rss/1.0/"><title>A Moving Target—Medicare Beneficiaries Coming to the End of Long Lives</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14916</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A Moving Target—Medicare Beneficiaries Coming to the End of Long Lives</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Joanne Lynn</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-05-09T00:01:02.069474-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14916</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14916</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14916</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Editorial</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1394</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1395</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14852" xmlns="http://purl.org/rss/1.0/"><title>John A. Hartford Foundation Centers of Excellence Program: History, Impact, and Legacy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14852</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">John A. Hartford Foundation Centers of Excellence Program: History, Impact, and Legacy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">David B. Reuben, Daniel B. Kaplan, Odette Willik, Nora O Brien-Suric</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-17T10:35:30.772863-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14852</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14852</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14852</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Special Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1396</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1400</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>The John A. Hartford Foundation (JAHF) created the Centers of Excellence in Geriatric Medicine and Geriatric Psychiatry in 1988 with the goal of establishing academic training environments to increase geriatrics-trained faculty. The initiative identified medical schools with the necessary components for training academic geriatricians. JAHF grants provided the resources to create a cadre of physicians whose research, teaching and practice leads to substantial contributions in geriatrics. Results from two evaluations show that the program has successfully increased geriatrics-prepared faculty who have achieved promotion and institutional retention, success in winning competitive research grants, and positions of leadership. The initiative strengthened the national network of geriatrics programs and served as a major driver of increased prestige for the fields of geriatric medicine and psychiatry.</p></div>
]]></content:encoded><description>
The John A. Hartford Foundation (JAHF) created the Centers of Excellence in Geriatric Medicine and Geriatric Psychiatry in 1988 with the goal of establishing academic training environments to increase geriatrics-trained faculty. The initiative identified medical schools with the necessary components for training academic geriatricians. JAHF grants provided the resources to create a cadre of physicians whose research, teaching and practice leads to substantial contributions in geriatrics. Results from two evaluations show that the program has successfully increased geriatrics-prepared faculty who have achieved promotion and institutional retention, success in winning competitive research grants, and positions of leadership. The initiative strengthened the national network of geriatrics programs and served as a major driver of increased prestige for the fields of geriatric medicine and psychiatry.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14887" xmlns="http://purl.org/rss/1.0/"><title>Recent Literature Update on Medication Risk in Older Adults, 2015–2016</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14887</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Recent Literature Update on Medication Risk in Older Adults, 2015–2016</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michael J. Koronkowski, Todd P. Semla, Kenneth E. Schmader, Joseph T. Hanlon</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-28T09:35:31.580727-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14887</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14887</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14887</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Special Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1401</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1405</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Medications can pose considerable risk in older adults. This article annotates four articles addressing this concern from 2016. The first provides national data on the use of specific prescription, over-the-counter and dietary supplements in older adults and their change over time. The second discusses the opportunity of deprescribing ineffective/unnecessary stool softeners (i.e., docusate) routinely given to older hospital patients. The third national study examines common adverse drug events in older emergency room patients. Finally, a study published demonstrating a potential association between melatonin and fractures is discussed. This manuscript is intended to provide a narrative review of key publications in medication safety for clinicians and researchers committed to improving medication safety in older adults.</p></div>
]]></content:encoded><description>
Medications can pose considerable risk in older adults. This article annotates four articles addressing this concern from 2016. The first provides national data on the use of specific prescription, over-the-counter and dietary supplements in older adults and their change over time. The second discusses the opportunity of deprescribing ineffective/unnecessary stool softeners (i.e., docusate) routinely given to older hospital patients. The third national study examines common adverse drug events in older emergency room patients. Finally, a study published demonstrating a potential association between melatonin and fractures is discussed. This manuscript is intended to provide a narrative review of key publications in medication safety for clinicians and researchers committed to improving medication safety in older adults.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14891" xmlns="http://purl.org/rss/1.0/"><title>End-of-Life Care Transition Patterns of Medicare Beneficiaries</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14891</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">End-of-Life Care Transition Patterns of Medicare Beneficiaries</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Shi-Yi Wang, Melissa D. Aldridge, Cary P. Gross, Maureen Canavan, Emily Cherlin, Elizabeth Bradley</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-04-03T10:10:37.493644-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14891</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14891</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14891</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1406</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1413</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14891-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To characterize the patterns of transitions in care and factors associated with multiple transitions in the last 6 months of life of U.S. decedents (N = 660,132).</p></div></div>
<div class="section" id="jgs14891-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Retrospective study.</p></div></div>
<div class="section" id="jgs14891-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>United States.</p></div></div>
<div class="section" id="jgs14891-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Medicare beneficiaries aged 66 and older who died from July to December 2011.</p></div></div>
<div class="section" id="jgs14891-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Transitions between healthcare settings (e.g., hospital, skilled nursing facility, inpatient hospice, home hospice, home without hospice) in the last 6 months of life. A count variable for number of transitions was summarized, and Sankey diagrams were produced to illustrate the sequences of healthcare transitions. Multivariable analyses were used to identify factors associated with likelihood of having four or more transitions.</p></div></div>
<div class="section" id="jgs14891-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>More than 80% decedents (n = 556,437) had at least one transition within the last 6 months of life; 218,731 had four or more transitions within the last 6 months of life. The most-frequent transition pattern (19.3% of all decedents; n = 127,435) was home to hospital, back to home or skilled nursing facility, to hospital again, and then to settings other than hospital, ending with four or more transitions. The average number of transitions in the last 6 months of life varied substantially across states, ranging from 1.8 in Alaska to 3.1 in New Jersey. Transitions became more intensive for decedents approaching death. In multivariable analyses, women, blacks, individuals younger than 85, and individuals without dementia were more likely to have four or more transitions (all <em>P</em> &lt; .05).</p></div></div>
<div class="section" id="jgs14891-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Approximately one-third of the Medicare beneficiaries who died in 2011 had four or more transitions within their last 6 months of life. Identifying interventions that can facilitate care transitions consistent with beneficiaries’ preferences is warranted.</p></div></div>
]]></content:encoded><description>

Objectives
To characterize the patterns of transitions in care and factors associated with multiple transitions in the last 6 months of life of U.S. decedents (N = 660,132).


Design
Retrospective study.


Setting
United States.


Participants
Medicare beneficiaries aged 66 and older who died from July to December 2011.


Measurements
Transitions between healthcare settings (e.g., hospital, skilled nursing facility, inpatient hospice, home hospice, home without hospice) in the last 6 months of life. A count variable for number of transitions was summarized, and Sankey diagrams were produced to illustrate the sequences of healthcare transitions. Multivariable analyses were used to identify factors associated with likelihood of having four or more transitions.


Results
More than 80% decedents (n = 556,437) had at least one transition within the last 6 months of life; 218,731 had four or more transitions within the last 6 months of life. The most-frequent transition pattern (19.3% of all decedents; n = 127,435) was home to hospital, back to home or skilled nursing facility, to hospital again, and then to settings other than hospital, ending with four or more transitions. The average number of transitions in the last 6 months of life varied substantially across states, ranging from 1.8 in Alaska to 3.1 in New Jersey. Transitions became more intensive for decedents approaching death. In multivariable analyses, women, blacks, individuals younger than 85, and individuals without dementia were more likely to have four or more transitions (all P &lt; .05).


Conclusion
Approximately one-third of the Medicare beneficiaries who died in 2011 had four or more transitions within their last 6 months of life. Identifying interventions that can facilitate care transitions consistent with beneficiaries’ preferences is warranted.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14795" xmlns="http://purl.org/rss/1.0/"><title>Falls and Frailty in Prostate Cancer Survivors: Current, Past, and Never Users of Androgen Deprivation Therapy</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14795</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Falls and Frailty in Prostate Cancer Survivors: Current, Past, and Never Users of Androgen Deprivation Therapy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kerri M. Winters-Stone, Esther Moe, Julie N. Graff, Nathan F. Dieckmann, Sydnee Stoyles, Carolyn Borsch, Joshi J. Alumkal, Christopher L. Amling, Tomasz M. Beer</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-06T10:30:44.317045-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14795</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14795</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14795</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1414</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1419</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14795-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To compare the prevalence of and association between falls and frailty of prostate cancer survivors (PCSs) who were current, past or never users of androgen deprivation therapy (ADT).</p></div></div>
<div class="section" id="jgs14795-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Cross-sectional.</p></div></div>
<div class="section" id="jgs14795-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Mail and electronic survey.</p></div></div>
<div class="section" id="jgs14795-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>PCSs (N = 280; mean age 72 ± 8).</p></div></div>
<div class="section" id="jgs14795-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Cancer history, falls, and frailty status (robust, prefrail, frail) using traditionally defined and obese phenotypes.</p></div></div>
<div class="section" id="jgs14795-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Current (37%) or past (34%) ADT users were more than twice as likely to have fallen in the previous year as never users (15%) (<em>P</em> = .002). ADT users had twice as many recurrent falls (<em>P</em> &lt; .001) and more fall-related injuries than unexposed men (<em>P</em> = .01). Current (43%) or past (40%) ADT users were more likely to be classified as prefrail or frail than never users (15%) (<em>P</em> &lt; .001), and the prevalence of combined obese frailty + prefrailty was even greater in current (59%) or past (62%) ADT users than never users (25%) (<em>P</em> &lt; .001). Traditional and obese frailty significantly increased the likelihood of reporting falls in the previous year (odds ratio (OR) = 2.15, 95% CI = 1.18–3.94 and OR = 2.97, 95% CI = 1.62–5.58, respectively) and was also associated with greater risk of recurrent falls (OR = 3.10, 95% CI = 1.48–6.5 and OR = 3.99, 95% CI = 1.79–8.89, respectively).</p></div></div>
<div class="section" id="jgs14795-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Current and past exposure to ADT is linked to higher risk of falls and frailty than no treatment. PCSs should be appropriately counseled on fall prevention strategies, and approaches to reduce frailty should be considered.</p></div></div>
]]></content:encoded><description>

Objectives
To compare the prevalence of and association between falls and frailty of prostate cancer survivors (PCSs) who were current, past or never users of androgen deprivation therapy (ADT).


Design
Cross-sectional.


Setting
Mail and electronic survey.


Participants
PCSs (N = 280; mean age 72 ± 8).


Measurements
Cancer history, falls, and frailty status (robust, prefrail, frail) using traditionally defined and obese phenotypes.


Results
Current (37%) or past (34%) ADT users were more than twice as likely to have fallen in the previous year as never users (15%) (P = .002). ADT users had twice as many recurrent falls (P &lt; .001) and more fall-related injuries than unexposed men (P = .01). Current (43%) or past (40%) ADT users were more likely to be classified as prefrail or frail than never users (15%) (P &lt; .001), and the prevalence of combined obese frailty + prefrailty was even greater in current (59%) or past (62%) ADT users than never users (25%) (P &lt; .001). Traditional and obese frailty significantly increased the likelihood of reporting falls in the previous year (odds ratio (OR) = 2.15, 95% CI = 1.18–3.94 and OR = 2.97, 95% CI = 1.62–5.58, respectively) and was also associated with greater risk of recurrent falls (OR = 3.10, 95% CI = 1.48–6.5 and OR = 3.99, 95% CI = 1.79–8.89, respectively).


Conclusions
Current and past exposure to ADT is linked to higher risk of falls and frailty than no treatment. PCSs should be appropriately counseled on fall prevention strategies, and approaches to reduce frailty should be considered.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14794" xmlns="http://purl.org/rss/1.0/"><title>Physical Abuse of Elderly Adults: Victim Characteristics and Determinants of Revictimization</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14794</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Physical Abuse of Elderly Adults: Victim Characteristics and Determinants of Revictimization</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lee S. Friedman, Susan Avila, Tazeen Rizvi, Renee Partida, Daniel Friedman</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-05-09T07:00:01.393971-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14794</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14794</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14794</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1420</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1426</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14794-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To describe victim characteristics and determinants of recurrent physical abuse of elderly.</p></div></div>
<div class="section" id="jgs14794-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Multicenter retrospective analysis of multiple data systems to study victims of elder mistreatment in the greater Chicago metropolitan area.</p></div></div>
<div class="section" id="jgs14794-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Five teaching hospitals with Level 1 trauma centers.</p></div></div>
<div class="section" id="jgs14794-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Individuals aged 60 and older treated for physical and sexual abuse between 2000 and 2011.</p></div></div>
<div class="section" id="jgs14794-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>History of revictimization was based on hospital admission histories, Adult Protective Services records, and self-report. Death records were also linked to participant files.</p></div></div>
<div class="section" id="jgs14794-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Fifty-eight individuals (52.3%) out of 111 cases suffering physical abuse had documented histories of revictimization. Based on multivariable models, individuals who were female, widowed, diagnosed with dementia, and returning to the home where the perpetrator lived or visited were substantially more likely to be revictimized. Revictimized individuals were more likely to be assaulted through unarmed force by a proximal relative, in particular a husband, boyfriend, child, or child-in-law. Based on hospital records, only 57% of community-dwelling cases had their abuse reported to Adult Protective Services or the police, and only 26.6% had Adult Protective Services investigations on record.</p></div></div>
<div class="section" id="jgs14794-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Better screening that connects victims of abuse with community services, police action, and alternative residential options is important in reducing the risk of revictimization and connecting individuals with resources that can improve their safety at home, regardless of whether it is in the community or a residential facility.</p></div></div>
]]></content:encoded><description>

Objectives
To describe victim characteristics and determinants of recurrent physical abuse of elderly.


Design
Multicenter retrospective analysis of multiple data systems to study victims of elder mistreatment in the greater Chicago metropolitan area.


Setting
Five teaching hospitals with Level 1 trauma centers.


Participants
Individuals aged 60 and older treated for physical and sexual abuse between 2000 and 2011.


Measurements
History of revictimization was based on hospital admission histories, Adult Protective Services records, and self-report. Death records were also linked to participant files.


Results
Fifty-eight individuals (52.3%) out of 111 cases suffering physical abuse had documented histories of revictimization. Based on multivariable models, individuals who were female, widowed, diagnosed with dementia, and returning to the home where the perpetrator lived or visited were substantially more likely to be revictimized. Revictimized individuals were more likely to be assaulted through unarmed force by a proximal relative, in particular a husband, boyfriend, child, or child-in-law. Based on hospital records, only 57% of community-dwelling cases had their abuse reported to Adult Protective Services or the police, and only 26.6% had Adult Protective Services investigations on record.


Conclusion
Better screening that connects victims of abuse with community services, police action, and alternative residential options is important in reducing the risk of revictimization and connecting individuals with resources that can improve their safety at home, regardless of whether it is in the community or a residential facility.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14804" xmlns="http://purl.org/rss/1.0/"><title>Effect of Physical Activity versus Health Education on Physical Function, Grip Strength and Mobility</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14804</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effect of Physical Activity versus Health Education on Physical Function, Grip Strength and Mobility</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Adam J. Santanasto, Nancy W. Glynn, Laura C. Lovato, Steven N. Blair, Roger A. Fielding, Thomas M. Gill, Jack M. Guralnik, Fang-Chi Hsu, Abby C. King, Elsa S. Strotmeyer, Todd M. Manini, Anthony P. Marsh, Mary M. McDermott, Bret H. Goodpaster, Marco Pahor, Anne B. Newman, </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-02-21T10:51:09.099906-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14804</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14804</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14804</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1427</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1433</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14804-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Background</h4><div class="para"><p>Physical activity (PA) reduces the rate of mobility disability, compared with health education (HE), in at risk older adults. It is important to understand aspects of performance contributing to this benefit.</p></div></div>
<div class="section" id="jgs14804-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To evaluate intervention effects on tertiary physical performance outcomes.</p></div></div>
<div class="section" id="jgs14804-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>The Lifestyle Interventions and Independence for Elders (LIFE) was a multi-centered, single-blind randomized trial of older adults.</p></div></div>
<div class="section" id="jgs14804-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Eight field centers throughout the United States.</p></div></div>
<div class="section" id="jgs14804-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>1635 adults aged 78.9 ± 5.2 years, 67.2% women at risk for mobility disability (Short Physical Performance Battery [SPPB] &lt;10).</p></div></div>
<div class="section" id="jgs14804-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Interventions</h4><div class="para"><p>Moderate PA including walking, resistance and balance training compared with HE consisting of topics relevant to older adults.</p></div></div>
<div class="section" id="jgs14804-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Outcomes</h4><div class="para"><p>Grip strength, SPPB score and its components (balance, 4 m gait speed, and chair-stands), as well as 400 m walking speed.</p></div></div>
<div class="section" id="jgs14804-sec-0008" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Total SPPB score was higher in PA versus HE across all follow-up times (overall <em>P</em> = .04) as was the chair-stand component (overall <em>P</em> &lt; .001). No intervention effects were observed for balance (overall <em>P</em> = .12), 4 m gait speed (overall <em>P</em> = .78), or grip strength (overall <em>P</em> = .62). However, 400 m walking speed was faster in PA versus HE group (overall <em>P</em> =&lt;.001). In separate models, 29% of the rate reduction of major mobility disability in the PA versus HE group was explained by change in SPPB score, while 39% was explained by change in the chair stand component.</p></div></div>
<div class="section" id="jgs14804-sec-0009" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Lower extremity performance (SPPB) was significantly higher in the PA compared with HE group. Changes in chair-stand score explained a considerable portion of the effect of PA on the reduction of major mobility disability–consistent with the idea that preserving muscle strength/power may be important for the prevention of major mobility disability.</p></div></div>
]]></content:encoded><description>

Background
Physical activity (PA) reduces the rate of mobility disability, compared with health education (HE), in at risk older adults. It is important to understand aspects of performance contributing to this benefit.


Objective
To evaluate intervention effects on tertiary physical performance outcomes.


Design
The Lifestyle Interventions and Independence for Elders (LIFE) was a multi-centered, single-blind randomized trial of older adults.


Setting
Eight field centers throughout the United States.


Participants
1635 adults aged 78.9 ± 5.2 years, 67.2% women at risk for mobility disability (Short Physical Performance Battery [SPPB] &lt;10).


Interventions
Moderate PA including walking, resistance and balance training compared with HE consisting of topics relevant to older adults.


Outcomes
Grip strength, SPPB score and its components (balance, 4 m gait speed, and chair-stands), as well as 400 m walking speed.


Results
Total SPPB score was higher in PA versus HE across all follow-up times (overall P = .04) as was the chair-stand component (overall P &lt; .001). No intervention effects were observed for balance (overall P = .12), 4 m gait speed (overall P = .78), or grip strength (overall P = .62). However, 400 m walking speed was faster in PA versus HE group (overall P =&lt;.001). In separate models, 29% of the rate reduction of major mobility disability in the PA versus HE group was explained by change in SPPB score, while 39% was explained by change in the chair stand component.


Conclusion
Lower extremity performance (SPPB) was significantly higher in the PA compared with HE group. Changes in chair-stand score explained a considerable portion of the effect of PA on the reduction of major mobility disability–consistent with the idea that preserving muscle strength/power may be important for the prevention of major mobility disability.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14811" xmlns="http://purl.org/rss/1.0/"><title>National Trends and Geographic Variation in Availability of Home Health Care: 2002–2015</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14811</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">National Trends and Geographic Variation in Availability of Home Health Care: 2002–2015</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yun Wang, Erica C. Leifheit-Limson, Jonathan Fine, Michelle M. Pandolfi, Yan Gao, Fanglin Liu, Sheila Eckenrode, Judith H. Lichtman</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-21T07:06:06.350684-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14811</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14811</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14811</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1434</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1440</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14811-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To evaluate national trends and geographic variation in the availability of home health care from 2002 to 2015 and identify county-specific characteristics associated with home health care.</p></div></div>
<div class="section" id="jgs14811-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Observational study.</p></div></div>
<div class="section" id="jgs14811-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>All counties in the United States.</p></div></div>
<div class="section" id="jgs14811-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>All Medicare-certified home health agencies included in the Centers for Medicare &amp; Medicaid Services Home Health Compare system.</p></div></div>
<div class="section" id="jgs14811-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>County-specific availability of home health care, defined as the number of available home health agencies that provided services to a given county per 100,000 population aged ≥18 years.</p></div></div>
<div class="section" id="jgs14811-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The study included 15,184 Medicare-certified home health agencies that served 97% of U.S. ZIP codes. Between 2002–2003 and 2014–2015, the county-specific number of available home health agencies per 100,000 population aged ≥18 years increased from 14.7 to 21.8 and the median (inter-quartile range) population that was serviced by at least one home health agency increased from 403,605 (890,329) to 455,488 (1,039,328). Considerable geographic variation in the availability of home health care was observed. The West, North East, and South Atlantic regions had lower home health care availability than the Central regions, and this pattern persisted over the study period. Counties with higher median income, a larger senior population, higher rates of households without a car and low access to stores, more obesity, greater inactivity, and higher proportions of non-Hispanic white, non-Hispanic black, and Hispanic populations were more likely to have higher availability of home health care.</p></div></div>
<div class="section" id="jgs14811-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>The availability of home health care increased nationwide during the study period, but there was much geographic variation.</p></div></div>
]]></content:encoded><description>

Objectives
To evaluate national trends and geographic variation in the availability of home health care from 2002 to 2015 and identify county-specific characteristics associated with home health care.


Design
Observational study.


Setting
All counties in the United States.


Participants
All Medicare-certified home health agencies included in the Centers for Medicare &amp; Medicaid Services Home Health Compare system.


Measurements
County-specific availability of home health care, defined as the number of available home health agencies that provided services to a given county per 100,000 population aged ≥18 years.


Results
The study included 15,184 Medicare-certified home health agencies that served 97% of U.S. ZIP codes. Between 2002–2003 and 2014–2015, the county-specific number of available home health agencies per 100,000 population aged ≥18 years increased from 14.7 to 21.8 and the median (inter-quartile range) population that was serviced by at least one home health agency increased from 403,605 (890,329) to 455,488 (1,039,328). Considerable geographic variation in the availability of home health care was observed. The West, North East, and South Atlantic regions had lower home health care availability than the Central regions, and this pattern persisted over the study period. Counties with higher median income, a larger senior population, higher rates of households without a car and low access to stores, more obesity, greater inactivity, and higher proportions of non-Hispanic white, non-Hispanic black, and Hispanic populations were more likely to have higher availability of home health care.


Conclusion
The availability of home health care increased nationwide during the study period, but there was much geographic variation.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14813" xmlns="http://purl.org/rss/1.0/"><title>Association of Proton Pump Inhibitors Usage with Risk of Pneumonia in Dementia Patients</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14813</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Association of Proton Pump Inhibitors Usage with Risk of Pneumonia in Dementia Patients</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sai-Wai Ho, Ying-Hock Teng, Shun-Fa Yang, Han-Wei Yeh, Yu-Hsun Wang, Ming-Chih Chou, Chao-Bin Yeh</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-21T00:01:02.458984-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14813</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14813</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14813</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1441</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1447</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14813-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To determine the association between usages of proton pump inhibitors (PPIs) and subsequent risk of pneumonia in dementia patients.</p></div></div>
<div class="section" id="jgs14813-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Retrospective cohort study.</p></div></div>
<div class="section" id="jgs14813-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Taiwanese National Health Insurance Research Database.</p></div></div>
<div class="section" id="jgs14813-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>The study cohort consisted of 786 dementia patients with new PPI usage and 786 matched dementia patients without PPI usage.</p></div></div>
<div class="section" id="jgs14813-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>The study endpoint was defined as the occurrence of pneumonia. The Cox proportional hazard model was used to estimate the pneumonia risk. Defined daily dose methodology was applied to evaluate the cumulative and dose-response relationships of PPI.</p></div></div>
<div class="section" id="jgs14813-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Incidence of pneumonia was higher among patients with PPI usage (adjusted hazard ratio (HR) = 1.89; 95% CI = 1.51–2.37). Cox model analysis also demonstrated that age (adjusted HR = 1.05; 95% CI = 1.03–1.06), male gender (adjusted HR = 1.57; 95% CI = 1.25–1.98), underlying cerebrovascular disease (adjusted HR = 1.30; 95% CI = 1.04–1.62), chronic pulmonary disease (adjusted HR = 1.39; 95% CI = 1.09–1.76), congestive heart failure (adjusted HR = 1.54; 95% CI = 1.11–2.13), diabetes mellitus (adjusted HR = 1.54; 95% CI = 1.22–1.95), and usage of antipsychotics (adjusted HR = 1.29; 95% CI = 1.03–1.61) were independent risk factors for pneumonia. However, usage of cholinesterase inhibitors and histamine receptor-2 antagonists were shown to decrease pneumonia risk.</p></div></div>
<div class="section" id="jgs14813-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>PPI usage in dementia patients is associated with an 89% increased risk of pneumonia.</p></div></div>
]]></content:encoded><description>

Objectives
To determine the association between usages of proton pump inhibitors (PPIs) and subsequent risk of pneumonia in dementia patients.


Design
Retrospective cohort study.


Setting
Taiwanese National Health Insurance Research Database.


Participants
The study cohort consisted of 786 dementia patients with new PPI usage and 786 matched dementia patients without PPI usage.


Measurements
The study endpoint was defined as the occurrence of pneumonia. The Cox proportional hazard model was used to estimate the pneumonia risk. Defined daily dose methodology was applied to evaluate the cumulative and dose-response relationships of PPI.


Results
Incidence of pneumonia was higher among patients with PPI usage (adjusted hazard ratio (HR) = 1.89; 95% CI = 1.51–2.37). Cox model analysis also demonstrated that age (adjusted HR = 1.05; 95% CI = 1.03–1.06), male gender (adjusted HR = 1.57; 95% CI = 1.25–1.98), underlying cerebrovascular disease (adjusted HR = 1.30; 95% CI = 1.04–1.62), chronic pulmonary disease (adjusted HR = 1.39; 95% CI = 1.09–1.76), congestive heart failure (adjusted HR = 1.54; 95% CI = 1.11–2.13), diabetes mellitus (adjusted HR = 1.54; 95% CI = 1.22–1.95), and usage of antipsychotics (adjusted HR = 1.29; 95% CI = 1.03–1.61) were independent risk factors for pneumonia. However, usage of cholinesterase inhibitors and histamine receptor-2 antagonists were shown to decrease pneumonia risk.


Conclusion
PPI usage in dementia patients is associated with an 89% increased risk of pneumonia.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14818" xmlns="http://purl.org/rss/1.0/"><title>Changes in Emergency Department Geriatric Services in Quebec and Correlates of These Changes</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14818</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Changes in Emergency Department Geriatric Services in Quebec and Correlates of These Changes</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jane McCusker, Alain Vadeboncoeur, Sylvie Cossette, Nathalie Veillette, Francine Ducharme, Thien Tuong Minh Vu, Antonio Ciampi, Deniz Cetin-Sahin, Eric Belzile</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-06T10:40:27.75794-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14818</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14818</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14818</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1448</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1454</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14818-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Background/Objectives</h4><div class="para"><p>To describe changes in geriatric emergency department (ED) services from 2006 (T1) to 2013/14 (T2), associated factors, and outcomes.</p></div></div>
<div class="section" id="jgs14818-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Two-wave survey design.</p></div></div>
<div class="section" id="jgs14818-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Province of Quebec, Canada.</p></div></div>
<div class="section" id="jgs14818-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Lead nurses and physicians at 57 EDs that participated in both the T1 and T2 surveys.</p></div></div>
<div class="section" id="jgs14818-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Intervention</h4><div class="para"><p>Changes over time in ED geriatric services, observed naturalistically.</p></div></div>
<div class="section" id="jgs14818-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Survey questionnaires assessed: ED geriatric services (11 items) and nursing and geriatric staffing resources. Key administrative data indicators for ED bed visits for T1 and T2 for ages 75 and over included: volume of ED visits; length of ED stay; admission rate; and 30-day return visits.</p></div></div>
<div class="section" id="jgs14818-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>There was a significant overall increase in the number ED geriatric services, from mean 2.8 (SD 2.2) at T1 to mean 6.0 (SD 2.0) at T2. EDs were clustered into 3 groups based on their T1 and T2 geriatric service scores: “early adopters” (n = 12); “late adopters” (n = 27); “non-adopters” (n = 18). Group membership was associated with three T1 variables: availability of a geriatric nurse clinician, a lower ratio of nurses to ED beds, and longer ED stays. There were significant overall increases between T1 and T2 in number of ED bed visits and ED length of stay among those aged 75 and over, decreases in hospitalization rates, but no change in ED return visits. There were no differential changes in the key indicators among the three ED clusters.</p></div></div>
<div class="section" id="jgs14818-sec-0008" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Overall, ED geriatric services improved in Quebec from 2006 to 2013/14. EDs with a geriatric nurse clinician, relatively fewer nursing resources, and longer ED stays improved more quickly.</p></div></div>
]]></content:encoded><description>

Background/Objectives
To describe changes in geriatric emergency department (ED) services from 2006 (T1) to 2013/14 (T2), associated factors, and outcomes.


Design
Two-wave survey design.


Setting
Province of Quebec, Canada.


Participants
Lead nurses and physicians at 57 EDs that participated in both the T1 and T2 surveys.


Intervention
Changes over time in ED geriatric services, observed naturalistically.


Measurements
Survey questionnaires assessed: ED geriatric services (11 items) and nursing and geriatric staffing resources. Key administrative data indicators for ED bed visits for T1 and T2 for ages 75 and over included: volume of ED visits; length of ED stay; admission rate; and 30-day return visits.


Results
There was a significant overall increase in the number ED geriatric services, from mean 2.8 (SD 2.2) at T1 to mean 6.0 (SD 2.0) at T2. EDs were clustered into 3 groups based on their T1 and T2 geriatric service scores: “early adopters” (n = 12); “late adopters” (n = 27); “non-adopters” (n = 18). Group membership was associated with three T1 variables: availability of a geriatric nurse clinician, a lower ratio of nurses to ED beds, and longer ED stays. There were significant overall increases between T1 and T2 in number of ED bed visits and ED length of stay among those aged 75 and over, decreases in hospitalization rates, but no change in ED return visits. There were no differential changes in the key indicators among the three ED clusters.


Conclusions
Overall, ED geriatric services improved in Quebec from 2006 to 2013/14. EDs with a geriatric nurse clinician, relatively fewer nursing resources, and longer ED stays improved more quickly.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14819" xmlns="http://purl.org/rss/1.0/"><title>Difficulty Managing Medications and Finances in Older Adults: A 10-year Cohort Study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14819</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Difficulty Managing Medications and Finances in Older Adults: A 10-year Cohort Study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nienke Bleijenberg, Alexander K. Smith, Sei J. Lee, Irena Stijacic Cenzer, John W. Boscardin, Kenneth E. Covinsky</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-04-05T00:01:06.33803-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14819</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14819</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14819</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1455</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1461</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14819-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Background</h4><div class="para"><p>Difficulty managing medicines and finances becomes increasingly common with advanced age, and compromises the ability to live safely and independently. Remarkably little is known how often this occurs.</p></div></div>
<div class="section" id="jgs14819-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To provide population-based estimates of the risk of developing incident difficulty managing medications and finances in older adults.</p></div></div>
<div class="section" id="jgs14819-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>A prospective cohort study.</p></div></div>
<div class="section" id="jgs14819-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>The Health and Retirement Study (HRS), a nationally representative study of older adults.</p></div></div>
<div class="section" id="jgs14819-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>9,434 participants aged 65 and older who did not need help in managing medications or managing finances in 2002. Follow-up assessments occurred every 2 years until 2012.</p></div></div>
<div class="section" id="jgs14819-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>The primary outcomes were time to difficulty managing medications and time to difficulty managing finances. Risk factors such as demographics, comorbidities, functional status, and cognitive status were assessed at baseline. Hazard models that considered the competing risk of death were used to estimate both the cumulative incidence of developing difficulty managing medications and finances and to identify potential risk factors. Analyses were adjusted for age, gender, race, marital status, wealth and education.</p></div></div>
<div class="section" id="jgs14819-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The 10 years incidence of difficulty increased markedly with age, ranging from 10.3% (95% CI 9.3–11.6) for managing medications and 23.1% (95% CI 21.6–24.7) for managing finances in those aged 65–69, to 38.2% (95% CI 33.4–43.5) for medicines and 69% (95% CI 63.7–74.3) for finances in those over age 85. Women had a higher probability of developing difficulty managing medications and managing finances than men.</p></div></div>
<div class="section" id="jgs14819-sec-0008" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>This study highlights the importance of preparing older adults for the likelihood they will need assistance with managing their medicines and finances as the risk for having difficulty with these activities over time is substantial.</p></div></div>
]]></content:encoded><description>

Background
Difficulty managing medicines and finances becomes increasingly common with advanced age, and compromises the ability to live safely and independently. Remarkably little is known how often this occurs.


Objectives
To provide population-based estimates of the risk of developing incident difficulty managing medications and finances in older adults.


Design
A prospective cohort study.


Setting
The Health and Retirement Study (HRS), a nationally representative study of older adults.


Participants
9,434 participants aged 65 and older who did not need help in managing medications or managing finances in 2002. Follow-up assessments occurred every 2 years until 2012.


Measurements
The primary outcomes were time to difficulty managing medications and time to difficulty managing finances. Risk factors such as demographics, comorbidities, functional status, and cognitive status were assessed at baseline. Hazard models that considered the competing risk of death were used to estimate both the cumulative incidence of developing difficulty managing medications and finances and to identify potential risk factors. Analyses were adjusted for age, gender, race, marital status, wealth and education.


Results
The 10 years incidence of difficulty increased markedly with age, ranging from 10.3% (95% CI 9.3–11.6) for managing medications and 23.1% (95% CI 21.6–24.7) for managing finances in those aged 65–69, to 38.2% (95% CI 33.4–43.5) for medicines and 69% (95% CI 63.7–74.3) for finances in those over age 85. Women had a higher probability of developing difficulty managing medications and managing finances than men.


Conclusion
This study highlights the importance of preparing older adults for the likelihood they will need assistance with managing their medicines and finances as the risk for having difficulty with these activities over time is substantial.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14812" xmlns="http://purl.org/rss/1.0/"><title>Mushroom Consumption and Incident Dementia in Elderly Japanese: The Ohsaki Cohort 2006 Study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14812</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Mushroom Consumption and Incident Dementia in Elderly Japanese: The Ohsaki Cohort 2006 Study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Shu Zhang, Yasutake Tomata, Kemmyo Sugiyama, Yumi Sugawara, Ichiro Tsuji</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-13T10:25:24.671245-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14812</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14812</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14812</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1462</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1469</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14812-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Background</h4><div class="para"><p>Both <em>in vivo</em> and <em>in vitro</em> studies have indicated that edible mushrooms may have preventive effects against cognitive impairment. However, few cohort studies have yet examined the relationship between mushroom consumption and incident dementia.</p></div></div>
<div class="section" id="jgs14812-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>We examined the relationship between mushroom consumption and incident dementia in a population of elderly Japanese subjects.</p></div></div>
<div class="section" id="jgs14812-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Prospective cohort study.</p></div></div>
<div class="section" id="jgs14812-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Ohsaki Cohort 2006 Study.</p></div></div>
<div class="section" id="jgs14812-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>13,230 individuals aged ≥65 years living in Ohsaki City, northeastern Japan.</p></div></div>
<div class="section" id="jgs14812-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Daily mushroom consumption, other lifestyle factors, and dementia incidence.</p></div></div>
<div class="section" id="jgs14812-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The 5.7 years incidence of dementia was 8.7%. In comparison with participants who consumed mushrooms &lt;1 time/wk, the multi-adjusted HRs (95% CI) for incident dementia among those did so 1–2 times/week and ≥3 times/week were 0.95 (0.81, 1.10) and 0.81 (0.69, 0.95), respectively (<em>P</em>-trend &lt;.01). The inverse association persisted after excluding participants whose dementia event occurred in the first 2 years of follow-up and whose baseline cognitive function was lower. The inverse association did not differ statistically in terms of vegetable consumption (<em>P</em>-interaction = .10).</p></div></div>
<div class="section" id="jgs14812-sec-0008" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>This cohort study suggests that frequent mushroom consumption is significantly associated with a lower risk of incident dementia, even after adjustment for possible confounding factors.</p></div></div>
]]></content:encoded><description>

Background
Both in vivo and in vitro studies have indicated that edible mushrooms may have preventive effects against cognitive impairment. However, few cohort studies have yet examined the relationship between mushroom consumption and incident dementia.


Objective
We examined the relationship between mushroom consumption and incident dementia in a population of elderly Japanese subjects.


Design
Prospective cohort study.


Setting
Ohsaki Cohort 2006 Study.


Participants
13,230 individuals aged ≥65 years living in Ohsaki City, northeastern Japan.


Measurements
Daily mushroom consumption, other lifestyle factors, and dementia incidence.


Results
The 5.7 years incidence of dementia was 8.7%. In comparison with participants who consumed mushrooms &lt;1 time/wk, the multi-adjusted HRs (95% CI) for incident dementia among those did so 1–2 times/week and ≥3 times/week were 0.95 (0.81, 1.10) and 0.81 (0.69, 0.95), respectively (P-trend &lt;.01). The inverse association persisted after excluding participants whose dementia event occurred in the first 2 years of follow-up and whose baseline cognitive function was lower. The inverse association did not differ statistically in terms of vegetable consumption (P-interaction = .10).


Conclusions
This cohort study suggests that frequent mushroom consumption is significantly associated with a lower risk of incident dementia, even after adjustment for possible confounding factors.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14823" xmlns="http://purl.org/rss/1.0/"><title>Delirium During Postacute Nursing Home Admission and Risk for Adverse Outcomes</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14823</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Delirium During Postacute Nursing Home Admission and Risk for Adverse Outcomes</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Cyrus M. Kosar, Kali S. Thomas, Sharon K. Inouye, Vincent Mor</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-24T07:15:50.128799-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14823</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14823</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14823</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1470</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1475</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14823-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To identify the rate of delirium present during admission to postacute care (PAC) in the nursing home setting and to determine whether patients with delirium had higher risk for adverse outcomes.</p></div></div>
<div class="section" id="jgs14823-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Retrospective cohort study.</p></div></div>
<div class="section" id="jgs14823-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>US Medicare- and Medicaid-certified nursing homes, 2011 to 2014.</p></div></div>
<div class="section" id="jgs14823-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Individuals admitted to all US nursing homes for PAC, aged ≥65 years, and without prior history of nursing home residence (n = 5,588,702).</p></div></div>
<div class="section" id="jgs14823-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Minimum Data Set (MDS) 3.0 admission assessments identified delirium based upon Confusion Assessment Method (CAM) items. Robust Poisson regression was used to calculate adjusted relative risks (aRRs) with 95% confidence intervals (CIs) for death following PAC admission, and for 30-day discharge outcomes including re-hospitalization from PAC, discharge home, and functional improvement.</p></div></div>
<div class="section" id="jgs14823-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Delirium was identified in 4.3% of new postacute nursing home admissions. Mortality within 30 days of PAC admission was observed in 16.3% of patients with delirium and 5.8% of patients without delirium (aRR = 2.27, CI = 2.24–2.30). The rate of 30-day readmission from PAC was 21.3% for patients with delirium compared with 15.1% among patients without delirium (aRR = 1.42, 95% CI = 1.40, 1.43). 26.9% of patients with delirium were discharged home within 30 days of admission compared to 52.5% of patients without delirium (aRR = 0.57, 95% CI = 0.57, 0.58). 48.9% of patients with delirium showed functional improvement at discharge compared to 59.9% of patients without delirium (aRR = 0.83, 95% CI = 0.82, 0.83).</p></div></div>
<div class="section" id="jgs14823-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>Patients with delirium present upon PAC admission were at high risk for mortality and 30-day re-hospitalization and were less likely to have timely discharge to home or to improve in physical function at discharge. Early identification and care planning for individuals with delirium at PAC admission may be essential to improve outcomes.</p></div></div>
]]></content:encoded><description>

Objectives
To identify the rate of delirium present during admission to postacute care (PAC) in the nursing home setting and to determine whether patients with delirium had higher risk for adverse outcomes.


Design
Retrospective cohort study.


Setting
US Medicare- and Medicaid-certified nursing homes, 2011 to 2014.


Participants
Individuals admitted to all US nursing homes for PAC, aged ≥65 years, and without prior history of nursing home residence (n = 5,588,702).


Measurements
Minimum Data Set (MDS) 3.0 admission assessments identified delirium based upon Confusion Assessment Method (CAM) items. Robust Poisson regression was used to calculate adjusted relative risks (aRRs) with 95% confidence intervals (CIs) for death following PAC admission, and for 30-day discharge outcomes including re-hospitalization from PAC, discharge home, and functional improvement.


Results
Delirium was identified in 4.3% of new postacute nursing home admissions. Mortality within 30 days of PAC admission was observed in 16.3% of patients with delirium and 5.8% of patients without delirium (aRR = 2.27, CI = 2.24–2.30). The rate of 30-day readmission from PAC was 21.3% for patients with delirium compared with 15.1% among patients without delirium (aRR = 1.42, 95% CI = 1.40, 1.43). 26.9% of patients with delirium were discharged home within 30 days of admission compared to 52.5% of patients without delirium (aRR = 0.57, 95% CI = 0.57, 0.58). 48.9% of patients with delirium showed functional improvement at discharge compared to 59.9% of patients without delirium (aRR = 0.83, 95% CI = 0.82, 0.83).


Conclusions
Patients with delirium present upon PAC admission were at high risk for mortality and 30-day re-hospitalization and were less likely to have timely discharge to home or to improve in physical function at discharge. Early identification and care planning for individuals with delirium at PAC admission may be essential to improve outcomes.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14810" xmlns="http://purl.org/rss/1.0/"><title>Diffuse Idiopathic Skeletal Hyperostosis (DISH) and Impaired Physical Function: The Rancho Bernardo Study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14810</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Diffuse Idiopathic Skeletal Hyperostosis (DISH) and Impaired Physical Function: The Rancho Bernardo Study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wendy B. Katzman, Mei-Hua Huang, Donna Kritz-Silverstein, Elizabeth Barrett-Connor, Deborah M. Kado</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-29T12:18:05.817339-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14810</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14810</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14810</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1476</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1481</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14810-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>Investigate associations of diffuse idiopathic skeletal hyperostosis (DISH) with self-reported and measured physical function in older adults.</p></div></div>
<div class="section" id="jgs14810-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Cross-sectional analyses of data collected in 1992–96 from a longitudinal cohort. Setting: Research clinic within a community.</p></div></div>
<div class="section" id="jgs14810-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Community-dwelling men (n = 630) and women (n = 961), mean age 71.5 years (SD = 10.8), from the Rancho Bernardo Study.</p></div></div>
<div class="section" id="jgs14810-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>DISH assessed from lateral thoracic and lumbar spine radiographs; self-reported difficulty bending over to the floor, walking 2–3 level blocks, or climbing 1 flight of stairs; performance-based measures of grip strength and chair-stand testing (ability to stand up and sit down in a chair 5 times without using chair arms).</p></div></div>
<div class="section" id="jgs14810-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>DISH was present in 25.6% of men and 5.5% of women. In age and sex-adjusted models, those with DISH had 1.72-fold increased odds (95% CI: 1.13, 2.62) of self-reported difficulty bending; this remained significant after further adjustment for Cobb angle, weight, stroke, arthritis, and exercise, OR = 1.69, (95% CI: 1.07, 2.66). In fully adjusted multivariate models, those with DISH had worse grip strength, −1.08 kg, <em>P</em> = .01, but did not differ from those without DISH on walking or climbing stairs. In sex-stratified, fully adjusted models, among men only, those with DISH were 2.17-times (95% CI: 1.04, 4.52) more likely to be unable to complete 5 chair stands without using their arms.</p></div></div>
<div class="section" id="jgs14810-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>DISH was less prevalent in women but affected almost one-quarter of older white men. People with DISH are more likely to experience physical functional impairment, suggesting that DISH has clinical correlations and is not an incidental radiographic finding.</p></div></div>
]]></content:encoded><description>

Objectives
Investigate associations of diffuse idiopathic skeletal hyperostosis (DISH) with self-reported and measured physical function in older adults.


Design
Cross-sectional analyses of data collected in 1992–96 from a longitudinal cohort. Setting: Research clinic within a community.


Participants
Community-dwelling men (n = 630) and women (n = 961), mean age 71.5 years (SD = 10.8), from the Rancho Bernardo Study.


Measurements
DISH assessed from lateral thoracic and lumbar spine radiographs; self-reported difficulty bending over to the floor, walking 2–3 level blocks, or climbing 1 flight of stairs; performance-based measures of grip strength and chair-stand testing (ability to stand up and sit down in a chair 5 times without using chair arms).


Results
DISH was present in 25.6% of men and 5.5% of women. In age and sex-adjusted models, those with DISH had 1.72-fold increased odds (95% CI: 1.13, 2.62) of self-reported difficulty bending; this remained significant after further adjustment for Cobb angle, weight, stroke, arthritis, and exercise, OR = 1.69, (95% CI: 1.07, 2.66). In fully adjusted multivariate models, those with DISH had worse grip strength, −1.08 kg, P = .01, but did not differ from those without DISH on walking or climbing stairs. In sex-stratified, fully adjusted models, among men only, those with DISH were 2.17-times (95% CI: 1.04, 4.52) more likely to be unable to complete 5 chair stands without using their arms.


Conclusions
DISH was less prevalent in women but affected almost one-quarter of older white men. People with DISH are more likely to experience physical functional impairment, suggesting that DISH has clinical correlations and is not an incidental radiographic finding.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14816" xmlns="http://purl.org/rss/1.0/"><title>Functional Status Modifies the Association of Blood Pressure with Death in Elders: Health and Retirement Study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14816</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Functional Status Modifies the Association of Blood Pressure with Death in Elders: Health and Retirement Study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Chenkai Wu, Ellen Smit, Carmen A. Peralta, Harini Sarathy, Michelle C. Odden</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-17T10:35:29.574057-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14816</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14816</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14816</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1482</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1489</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14816-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objective</h4><div class="para"><p>To examine whether grip strength, gait speed, and the combination of the two physical functioning measures modified the association of systolic BP (SBP) and diastolic BP (DBP) with mortality.</p></div></div>
<div class="section" id="jgs14816-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Nationally representative cohort study.</p></div></div>
<div class="section" id="jgs14816-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Health and Retirement Study.</p></div></div>
<div class="section" id="jgs14816-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>7,492 U.S. adults aged ≥65 years.</p></div></div>
<div class="section" id="jgs14816-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Grip strength was measured by a hand dynamometer and classified as normal (≥16 kg for female; ≥26 kg for male) and weak. Gait speed was assessed over a 98.5-inch walk and classified as non-slow (≥0.60 m/s for female; ≥0.52 m/s for male) and slow.</p></div></div>
<div class="section" id="jgs14816-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Over an average follow-up time of 6.0 years, 1,870 (25.0%) participants died. After adjustment for socio-demographic, behavioral, and clinical measures, elevated SBP (≥150 mmHg) and DBP (≥90 mmHg) was associated with a 24% (95% CI, 7–43%) and 25% (95% CI, 5–49%) higher mortality among participants with normal grip strength. In contrast, elevated SBP and DBP was associated with a 6% (95% CI, 31 to −27%) and a 16% (95% CI, 46 to −26%) lower mortality among those with weak grip strength (<em>P-</em>values of interactions: both=.07). The inverse relations between BP with death were most pronounced among slow walkers with weak grip strength. The HRs of elevated SBP and DBP for death was 0.85 (95% CI, 0.56–1.29) and 0.53 (95% CI, 0.30–0.96), respectively, and was substantially different from non-slow walkers with normal grip strength (HR = 1.24 and 1.15, respectively; <em>P-</em>values of interactions: both &lt;.001). Therefore, associations of BP with death varied modestly by gait speed.</p></div></div>
<div class="section" id="jgs14816-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Grip strength modified the association of BP with death. Combination of grip strength and gait speed has incremental value for modifying the association of BP with death.</p></div></div>
]]></content:encoded><description>

Objective
To examine whether grip strength, gait speed, and the combination of the two physical functioning measures modified the association of systolic BP (SBP) and diastolic BP (DBP) with mortality.


Design
Nationally representative cohort study.


Setting
Health and Retirement Study.


Participants
7,492 U.S. adults aged ≥65 years.


Measurements
Grip strength was measured by a hand dynamometer and classified as normal (≥16 kg for female; ≥26 kg for male) and weak. Gait speed was assessed over a 98.5-inch walk and classified as non-slow (≥0.60 m/s for female; ≥0.52 m/s for male) and slow.


Results
Over an average follow-up time of 6.0 years, 1,870 (25.0%) participants died. After adjustment for socio-demographic, behavioral, and clinical measures, elevated SBP (≥150 mmHg) and DBP (≥90 mmHg) was associated with a 24% (95% CI, 7–43%) and 25% (95% CI, 5–49%) higher mortality among participants with normal grip strength. In contrast, elevated SBP and DBP was associated with a 6% (95% CI, 31 to −27%) and a 16% (95% CI, 46 to −26%) lower mortality among those with weak grip strength (P-values of interactions: both=.07). The inverse relations between BP with death were most pronounced among slow walkers with weak grip strength. The HRs of elevated SBP and DBP for death was 0.85 (95% CI, 0.56–1.29) and 0.53 (95% CI, 0.30–0.96), respectively, and was substantially different from non-slow walkers with normal grip strength (HR = 1.24 and 1.15, respectively; P-values of interactions: both &lt;.001). Therefore, associations of BP with death varied modestly by gait speed.


Conclusion
Grip strength modified the association of BP with death. Combination of grip strength and gait speed has incremental value for modifying the association of BP with death.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14826" xmlns="http://purl.org/rss/1.0/"><title>Variation in Hospice Services by Location of Care: Nursing Home Versus Assisted Living Facility Versus Home</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14826</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Variation in Hospice Services by Location of Care: Nursing Home Versus Assisted Living Facility Versus Home</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kathleen T. Unroe, Brittany Bernard, Timothy E. Stump, Wanzhu Tu, Christopher M. Callahan</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-14T00:01:00.999849-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14826</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14826</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14826</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1490</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1496</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14826-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To describe differences in hospice services for patients living at home, in nursing homes or in assisted living facilities, including the overall number and duration of visits by different hospice care providers across varying lengths of stay.</p></div></div>
<div class="section" id="jgs14826-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Retrospective cohort study using hospice patient electronic medical record data.</p></div></div>
<div class="section" id="jgs14826-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Large, national hospice provider.</p></div></div>
<div class="section" id="jgs14826-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Data from 32,605 hospice patients who received routine hospice care from 2009 to 2014 were analyzed.</p></div></div>
<div class="section" id="jgs14826-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Descriptive statistics were calculated for utilization measures for each type of provider and by location of care. Frequency and duration of service contacts were standardized to a 1 week period and pairwise comparisons were used to detect differences in care provided between the three settings.</p></div></div>
<div class="section" id="jgs14826-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Minimal differences were found in overall intensity of service contacts across settings, however, the mix of services were different for patients living at home versus nursing home versus assisted living facility. Overall, more nurse care was provided at the beginning and end of the hospice episode; intensity of aide care services was higher in the middle portion of the hospice episode. Nearly 43% of the sample had hospice stays less than 2 weeks and up to 20% had stays greater than 6 months.</p></div></div>
<div class="section" id="jgs14826-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>There are significant differences between characteristics of hospice patients in different settings, as well as the mix of services they receive. Medicare hospice payment methodology was revised starting in 2016. While the new payment structure is in greater alignment with the U shape distribution of services, it will be important to evaluate the impact of the new payment methodology on length of stay and mix of services by different providers across settings of care.</p></div></div>
]]></content:encoded><description>

Objectives
To describe differences in hospice services for patients living at home, in nursing homes or in assisted living facilities, including the overall number and duration of visits by different hospice care providers across varying lengths of stay.


Design
Retrospective cohort study using hospice patient electronic medical record data.


Setting
Large, national hospice provider.


Participants
Data from 32,605 hospice patients who received routine hospice care from 2009 to 2014 were analyzed.


Measurements
Descriptive statistics were calculated for utilization measures for each type of provider and by location of care. Frequency and duration of service contacts were standardized to a 1 week period and pairwise comparisons were used to detect differences in care provided between the three settings.


Results
Minimal differences were found in overall intensity of service contacts across settings, however, the mix of services were different for patients living at home versus nursing home versus assisted living facility. Overall, more nurse care was provided at the beginning and end of the hospice episode; intensity of aide care services was higher in the middle portion of the hospice episode. Nearly 43% of the sample had hospice stays less than 2 weeks and up to 20% had stays greater than 6 months.


Conclusion
There are significant differences between characteristics of hospice patients in different settings, as well as the mix of services they receive. Medicare hospice payment methodology was revised starting in 2016. While the new payment structure is in greater alignment with the U shape distribution of services, it will be important to evaluate the impact of the new payment methodology on length of stay and mix of services by different providers across settings of care.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14827" xmlns="http://purl.org/rss/1.0/"><title>Adherence and Tolerability of Alzheimer's Disease Medications: A Pragmatic Randomized Trial</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14827</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Adherence and Tolerability of Alzheimer's Disease Medications: A Pragmatic Randomized Trial</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Noll L. Campbell, Anthony J. Perkins, Sujuan Gao, Todd C. Skaar, Lang Li, Hugh C. Hendrie, Nicole Fowler, Christopher M. Callahan, Malaz A. Boustani</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-14T10:50:28.327542-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14827</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14827</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14827</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1497</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1504</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14827-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Background/Objectives</h4><div class="para"><p>Post-marketing comparative trials describe medication use patterns in diverse, real-world populations. Our objective was to determine if differences in rates of adherence and tolerability exist among new users to acetylcholinesterase inhibitors (AChEI's).</p></div></div>
<div class="section" id="jgs14827-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Pragmatic randomized, open label comparative trial of AChEI's currently available in the United States.</p></div></div>
<div class="section" id="jgs14827-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Four memory care practices within four healthcare systems in the greater Indianapolis area.</p></div></div>
<div class="section" id="jgs14827-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Eligibility criteria included older adults with a diagnosis of possible or probable Alzheimer's disease (AD) who were initiating treatment with an AChEI. Participants were required to have a caregiver to complete assessments, access to a telephone, and be able to understand English. Exclusion criteria consisted of a prior severe adverse event from AChEIs.</p></div></div>
<div class="section" id="jgs14827-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Intervention</h4><div class="para"><p>Participants were randomized to one of three AChEIs in a 1:1:1 ratio and followed for 18 weeks.</p></div></div>
<div class="section" id="jgs14827-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Caregiver-reported adherence, defined as taking or not taking study medication, and caregiver-reported adverse events, defined as the presence of an adverse event.</p></div></div>
<div class="section" id="jgs14827-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>196 participants were included with 74.0% female, 30.6% African Americans, and 72.9% who completed at least twelfth grade. Discontinuation rates after 18 weeks were 38.8% for donepezil, 53.0% for galantamine, and 58.7% for rivastigmine (<em>P</em> = .063) in the intent to treat analysis. Adverse events and cost explained 73.1% and 25.4% of discontinuation. No participants discontinued donepezil due to cost. Adverse events were reported by 81.2% of all participants; no between-group differences in total adverse events were statistically significant.</p></div></div>
<div class="section" id="jgs14827-sec-0008" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>This pragmatic comparative trial showed high rates of adverse events and cost-related non-adherence with AChEIs. Interventions improving adherence and persistence to AChEIs may improve AD management. Trial Registration: Clinicaltrials.gov: NCT01362686 (<!--TODO: clickthrough URL--><a href="https://clinicaltrials.gov/ct2/show/NCT01362686" title="Link to external resource: https://clinicaltrials.gov/ct2/show/NCT01362686">https://clinicaltrials.gov/ct2/show/NCT01362686</a>).</p></div></div>
]]></content:encoded><description>

Background/Objectives
Post-marketing comparative trials describe medication use patterns in diverse, real-world populations. Our objective was to determine if differences in rates of adherence and tolerability exist among new users to acetylcholinesterase inhibitors (AChEI's).


Design
Pragmatic randomized, open label comparative trial of AChEI's currently available in the United States.


Setting
Four memory care practices within four healthcare systems in the greater Indianapolis area.


Participants
Eligibility criteria included older adults with a diagnosis of possible or probable Alzheimer's disease (AD) who were initiating treatment with an AChEI. Participants were required to have a caregiver to complete assessments, access to a telephone, and be able to understand English. Exclusion criteria consisted of a prior severe adverse event from AChEIs.


Intervention
Participants were randomized to one of three AChEIs in a 1:1:1 ratio and followed for 18 weeks.


Measurements
Caregiver-reported adherence, defined as taking or not taking study medication, and caregiver-reported adverse events, defined as the presence of an adverse event.


Results
196 participants were included with 74.0% female, 30.6% African Americans, and 72.9% who completed at least twelfth grade. Discontinuation rates after 18 weeks were 38.8% for donepezil, 53.0% for galantamine, and 58.7% for rivastigmine (P = .063) in the intent to treat analysis. Adverse events and cost explained 73.1% and 25.4% of discontinuation. No participants discontinued donepezil due to cost. Adverse events were reported by 81.2% of all participants; no between-group differences in total adverse events were statistically significant.


Conclusions
This pragmatic comparative trial showed high rates of adverse events and cost-related non-adherence with AChEIs. Interventions improving adherence and persistence to AChEIs may improve AD management. Trial Registration: Clinicaltrials.gov: NCT01362686 (https://clinicaltrials.gov/ct2/show/NCT01362686).

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14834" xmlns="http://purl.org/rss/1.0/"><title>Determinants of Dropout and Nonadherence in a Dementia Prevention Randomized Controlled Trial: The Prevention of Dementia by Intensive Vascular Care Trial</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14834</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Determinants of Dropout and Nonadherence in a Dementia Prevention Randomized Controlled Trial: The Prevention of Dementia by Intensive Vascular Care Trial</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Cathrien R. L. Beishuizen, Nicola Coley, Eric P. Moll van Charante, Willem A. Gool, Edo Richard, Sandrine Andrieu</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-06T10:40:35.115461-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14834</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14834</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14834</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1505</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1513</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14834-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To explore and compare sociodemographic, clinical, and neuropsychiatric determinants of dropout and nonadherence in older people participating in an open-label cluster-randomized controlled trial—the Prevention of Dementia by Intensive Vascular care (preDIVA) trial—over 6 years.</p></div></div>
<div class="section" id="jgs14834-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Secondary analysis.</p></div></div>
<div class="section" id="jgs14834-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>One hundred sixteen general practices in the Netherlands.</p></div></div>
<div class="section" id="jgs14834-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Community-dwelling individuals aged 70 to 78 (N = 2,994).</p></div></div>
<div class="section" id="jgs14834-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Intervention</h4><div class="para"><p>Nurse-led multidomain intervention targeting cardiovascular risk factors to prevent dementia.</p></div></div>
<div class="section" id="jgs14834-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>The associations between participant baseline sociodemographic (age, sex, education), clinical (medical history, disability, cardiovascular risk), neuropsychiatric (depressive symptoms (Geriatric Depression Scale-15), and cognitive (Mini-Mental State Examination)) characteristics and dropout from the trial and nonadherence to the trial intervention were explored using multilevel logistic regression models.</p></div></div>
<div class="section" id="jgs14834-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Older age, poorer cognitive function, more symptoms of depression, and greater disability were the most important determinants of dropout of older people. The presence of cardiovascular risk factors was not associated with dropout but was associated with nonadherence. Being overweight was a risk factor for nonadherence, whereas people with high blood pressure or a low level of physical exercise adhered better to the intervention. The association between poorer cognitive function and symptoms of depression and dropout was stronger in the control group than in the intervention group, and vice versa for increased disability.</p></div></div>
<div class="section" id="jgs14834-sec-0008" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>In a large dementia prevention trial with 6-year follow-up, dropout was associated with older age, poorer cognitive function, symptoms of depression, and disability at baseline. These findings can help to guide the design of future dementia prevention trials in older adults. The associations found between cardiovascular risk factors and nonadherence need to be confirmed in other older populations receiving cardiovascular prevention interventions.</p></div></div>
]]></content:encoded><description>

Objectives
To explore and compare sociodemographic, clinical, and neuropsychiatric determinants of dropout and nonadherence in older people participating in an open-label cluster-randomized controlled trial—the Prevention of Dementia by Intensive Vascular care (preDIVA) trial—over 6 years.


Design
Secondary analysis.


Setting
One hundred sixteen general practices in the Netherlands.


Participants
Community-dwelling individuals aged 70 to 78 (N = 2,994).


Intervention
Nurse-led multidomain intervention targeting cardiovascular risk factors to prevent dementia.


Measurements
The associations between participant baseline sociodemographic (age, sex, education), clinical (medical history, disability, cardiovascular risk), neuropsychiatric (depressive symptoms (Geriatric Depression Scale-15), and cognitive (Mini-Mental State Examination)) characteristics and dropout from the trial and nonadherence to the trial intervention were explored using multilevel logistic regression models.


Results
Older age, poorer cognitive function, more symptoms of depression, and greater disability were the most important determinants of dropout of older people. The presence of cardiovascular risk factors was not associated with dropout but was associated with nonadherence. Being overweight was a risk factor for nonadherence, whereas people with high blood pressure or a low level of physical exercise adhered better to the intervention. The association between poorer cognitive function and symptoms of depression and dropout was stronger in the control group than in the intervention group, and vice versa for increased disability.


Conclusion
In a large dementia prevention trial with 6-year follow-up, dropout was associated with older age, poorer cognitive function, symptoms of depression, and disability at baseline. These findings can help to guide the design of future dementia prevention trials in older adults. The associations found between cardiovascular risk factors and nonadherence need to be confirmed in other older populations receiving cardiovascular prevention interventions.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14829" xmlns="http://purl.org/rss/1.0/"><title>Life-Space Mobility and Cognitive Decline Among Mexican Americans Aged 75 Years and Older</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14829</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Life-Space Mobility and Cognitive Decline Among Mexican Americans Aged 75 Years and Older</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Seraina Silberschmidt, Amit Kumar, Mukaila M. Raji, Kyriakos Markides, Kenneth J. Ottenbacher, Soham Al Snih</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-09T00:40:30.385859-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14829</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14829</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14829</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1514</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1520</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14829-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To examine the association between life-space mobility and cognitive decline over a five-year period among older Mexican Americans.</p></div></div>
<div class="section" id="jgs14829-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Longitudinal study.</p></div></div>
<div class="section" id="jgs14829-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Hispanic Established Population for the Epidemiologic Study of the Elderly survey conducted in the southwestern of United States (Texas, Colorado, Arizona, New Mexico, and California).</p></div></div>
<div class="section" id="jgs14829-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Four hundred thirty-two Mexican Americans aged 75 and older with normal or high cognitive function at baseline.</p></div></div>
<div class="section" id="jgs14829-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Socio-demographic factors, living arrangement, type of household, social support, financial strain, self-reported medical conditions, Mini-Mental State Examination (MMSE), depressive symptoms, activities of daily living (ADLs), and Short Physical Performance Battery. Life-space assessment (LSA) during the past 4 weeks was assessed during in-home interview. Scores ranged from 0 (daily restriction to the bedroom) to 120 (daily trips outside of their own town without assistance) and categorized as 0 to 20, 21 to 40, 41 to 60, 61 to 80, and 81 to 120. Because of the small sample size in the category of 81 to 120, the two highest categories were combined into a single group.</p></div></div>
<div class="section" id="jgs14829-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The mean LSA score and MMSE score of participants at baseline was 44.6 (Standard Deviation [SD], 20.7) and 25.7 (SD, 3.2), respectively. Mixed Model analyses showed that participants in the highest life-space category (≥61) experienced slower rates of cognitive decline over time compared to participants in the lowest category (0 to 20) (<em>β</em> = 1.03, Standard Error [SE] = 0.29, <em>P</em> = 0.0004), after adjusting for all covariates.</p></div></div>
<div class="section" id="jgs14829-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Greater life-space mobility at baseline was predictor of slower rates of cognitive decline over 5 years in older Mexican Americans.</p></div></div>
]]></content:encoded><description>

Objectives
To examine the association between life-space mobility and cognitive decline over a five-year period among older Mexican Americans.


Design
Longitudinal study.


Setting
Hispanic Established Population for the Epidemiologic Study of the Elderly survey conducted in the southwestern of United States (Texas, Colorado, Arizona, New Mexico, and California).


Participants
Four hundred thirty-two Mexican Americans aged 75 and older with normal or high cognitive function at baseline.


Measurements
Socio-demographic factors, living arrangement, type of household, social support, financial strain, self-reported medical conditions, Mini-Mental State Examination (MMSE), depressive symptoms, activities of daily living (ADLs), and Short Physical Performance Battery. Life-space assessment (LSA) during the past 4 weeks was assessed during in-home interview. Scores ranged from 0 (daily restriction to the bedroom) to 120 (daily trips outside of their own town without assistance) and categorized as 0 to 20, 21 to 40, 41 to 60, 61 to 80, and 81 to 120. Because of the small sample size in the category of 81 to 120, the two highest categories were combined into a single group.


Results
The mean LSA score and MMSE score of participants at baseline was 44.6 (Standard Deviation [SD], 20.7) and 25.7 (SD, 3.2), respectively. Mixed Model analyses showed that participants in the highest life-space category (≥61) experienced slower rates of cognitive decline over time compared to participants in the lowest category (0 to 20) (β = 1.03, Standard Error [SE] = 0.29, P = 0.0004), after adjusting for all covariates.


Conclusion
Greater life-space mobility at baseline was predictor of slower rates of cognitive decline over 5 years in older Mexican Americans.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14837" xmlns="http://purl.org/rss/1.0/"><title>Posttraumatic Stress Disorder, Antipsychotic Use and Risk of Dementia in Veterans</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14837</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Posttraumatic Stress Disorder, Antipsychotic Use and Risk of Dementia in Veterans</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Elizabeth E. Roughead, Nicole L. Pratt, Lisa M. Kalisch Ellett, Emmae N. Ramsay, John D. Barratt, Philip Morris, Graeme Killer</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-17T10:20:26.850109-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14837</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14837</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14837</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1521</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1526</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14837-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To examine the risk of dementia associated with posttraumatic stress disorder (PTSD) and the contribution of antipsychotic use to this risk.</p></div></div>
<div class="section" id="jgs14837-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Retrospective cohort study</p></div></div>
<div class="section" id="jgs14837-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Australia. Administrative claims data from the Australian Government Department of Veterans' Affairs were used.</p></div></div>
<div class="section" id="jgs14837-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Male Vietnam veterans aged 55 to 65 at baseline (2001–02) with no preexisting dementia diagnosis (N = 15,612).</p></div></div>
<div class="section" id="jgs14837-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>The association between PTSD and dementia was assessed over 12 years of follow-up. Dementia was identified as a hospital diagnosis, dementia record in service disability data, or dispensing of medicines for dementia. Cox-proportional hazards models were used, with age as the time-scale. Results were stratified according to baseline antipsychotic use.</p></div></div>
<div class="section" id="jgs14837-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>No greater risk of dementia was observed with PTSD. In veterans who received antipsychotics, dementia risk was significantly higher than in those who did not (hazard ratio (HR) = 2.1, 95% confidence interval (CI) = 1.4–3.3). Dementia risk was significantly greater in veterans hospitalized for PTSD who received antipsychotics (HR = 2.2, 95% CI = 1.1–4.6) and veterans without PTSD who received antipsychotics (HR = 4.3, 95% CI = 2.1–8.6) than in those without PTSD with no antipsychotic use.</p></div></div>
<div class="section" id="jgs14837-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Antipsychotic use may be a contributor to dementia risk. These findings should be interpreted with caution because the study design was observational. Further research using prospective study designs in settings where diagnostic data, cognitive function, and disease severity are available are required.</p></div></div>
]]></content:encoded><description>

Objectives
To examine the risk of dementia associated with posttraumatic stress disorder (PTSD) and the contribution of antipsychotic use to this risk.


Design
Retrospective cohort study


Setting
Australia. Administrative claims data from the Australian Government Department of Veterans' Affairs were used.


Participants
Male Vietnam veterans aged 55 to 65 at baseline (2001–02) with no preexisting dementia diagnosis (N = 15,612).


Measurements
The association between PTSD and dementia was assessed over 12 years of follow-up. Dementia was identified as a hospital diagnosis, dementia record in service disability data, or dispensing of medicines for dementia. Cox-proportional hazards models were used, with age as the time-scale. Results were stratified according to baseline antipsychotic use.


Results
No greater risk of dementia was observed with PTSD. In veterans who received antipsychotics, dementia risk was significantly higher than in those who did not (hazard ratio (HR) = 2.1, 95% confidence interval (CI) = 1.4–3.3). Dementia risk was significantly greater in veterans hospitalized for PTSD who received antipsychotics (HR = 2.2, 95% CI = 1.1–4.6) and veterans without PTSD who received antipsychotics (HR = 4.3, 95% CI = 2.1–8.6) than in those without PTSD with no antipsychotic use.


Conclusion
Antipsychotic use may be a contributor to dementia risk. These findings should be interpreted with caution because the study design was observational. Further research using prospective study designs in settings where diagnostic data, cognitive function, and disease severity are available are required.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14838" xmlns="http://purl.org/rss/1.0/"><title>Effect of Clostridium difficile Prevalence in Hospitals and Nursing Homes on Risk of Infection</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14838</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effect of Clostridium difficile Prevalence in Hospitals and Nursing Homes on Risk of Infection</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nina R. Joyce, Eleftherios Mylonakis, Vincent Mor</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-04-10T09:35:44.893686-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14838</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14838</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14838</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1527</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1534</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14838-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To assess the effect of facility <em>Clostridium difficile</em> infection (CDI) prevalence on risk of healthcare facility (HFC) acquired CDI.</p></div></div>
<div class="section" id="jgs14838-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Retrospective cohort study.</p></div></div>
<div class="section" id="jgs14838-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Medicare fee-for-service (FFS) claims and skilled nursing facility (SNF) Minimum Data Set 3.0 assessments.</p></div></div>
<div class="section" id="jgs14838-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Medicare beneficiaries with 90 days or more of no contact with a HCF before a hospital admission without a CDI diagnosis. Participants were separated into two cohorts: discharged to the community and discharged to a SNF.</p></div></div>
<div class="section" id="jgs14838-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Risk of HCF-acquired CDI associated with CDI prevalence at the index facility measured according to 30-day rehospitalization with a discharge diagnosis of CDI or diagnosis in the SNF after admission. Hospital and SNF CDI prevalence were categorized into three groups: 0% and above and below the median value for facilities with greater than 0% prevalence.</p></div></div>
<div class="section" id="jgs14838-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Of 817,900 eligible individuals, there were 553,423 admissions in the first cohort (discharged to the community) and 315,109 in the second (discharged to a SNF). In the first cohort, the risk of HCF-acquired CDI was higher for individuals admitted to hospitals with CDI prevalence less than the median (relative risk (RR) = 1.58, 95% confidence interval (CI) = 1.18–2.12) and greater than the median (RR = 2.56, 95% CI = 1.91–3.45) than for those with no CDI. In the second cohort, the risk of HCF-acquired CDI was greater for individuals admitted to a hospital (RR = 1.89, 95% CI = 1.49–2.39) and a SNF (RR = 1.48, 95% CI = 1.31–1.67) with CDI prevalence greater than the median.</p></div></div>
<div class="section" id="jgs14838-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>The risk of HCF-acquired CDI is greater for noninfected individuals admitted to hospitals and SNFs with a high prevalence of CDI.</p></div></div>
]]></content:encoded><description>

Objectives
To assess the effect of facility Clostridium difficile infection (CDI) prevalence on risk of healthcare facility (HFC) acquired CDI.


Design
Retrospective cohort study.


Setting
Medicare fee-for-service (FFS) claims and skilled nursing facility (SNF) Minimum Data Set 3.0 assessments.


Participants
Medicare beneficiaries with 90 days or more of no contact with a HCF before a hospital admission without a CDI diagnosis. Participants were separated into two cohorts: discharged to the community and discharged to a SNF.


Measurements
Risk of HCF-acquired CDI associated with CDI prevalence at the index facility measured according to 30-day rehospitalization with a discharge diagnosis of CDI or diagnosis in the SNF after admission. Hospital and SNF CDI prevalence were categorized into three groups: 0% and above and below the median value for facilities with greater than 0% prevalence.


Results
Of 817,900 eligible individuals, there were 553,423 admissions in the first cohort (discharged to the community) and 315,109 in the second (discharged to a SNF). In the first cohort, the risk of HCF-acquired CDI was higher for individuals admitted to hospitals with CDI prevalence less than the median (relative risk (RR) = 1.58, 95% confidence interval (CI) = 1.18–2.12) and greater than the median (RR = 2.56, 95% CI = 1.91–3.45) than for those with no CDI. In the second cohort, the risk of HCF-acquired CDI was greater for individuals admitted to a hospital (RR = 1.89, 95% CI = 1.49–2.39) and a SNF (RR = 1.48, 95% CI = 1.31–1.67) with CDI prevalence greater than the median.


Conclusion
The risk of HCF-acquired CDI is greater for noninfected individuals admitted to hospitals and SNFs with a high prevalence of CDI.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14844" xmlns="http://purl.org/rss/1.0/"><title>Use of Medications of Questionable Benefit at the End of Life in Nursing Home Residents with Advanced Dementia</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14844</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Use of Medications of Questionable Benefit at the End of Life in Nursing Home Residents with Advanced Dementia</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jeremy N. Matlow, Susan E. Bronskill, Andrea Gruneir, Chaim M. Bell, Nathan M. Stall, Nathan Herrmann, Dallas P. Seitz, Sudeep S. Gill, Peter C. Austin, Hadas D. Fischer, Kinwah Fung, Wei Wu, Paula A. Rochon</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-29T00:01:02.89896-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14844</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14844</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14844</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Investigation</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1535</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1542</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14844-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To determine the prevalence of and resident characteristics associated with the prescription of medications of questionable benefit (MQBs) near the end of life in older adults with advanced dementia in nursing homes.</p></div></div>
<div class="section" id="jgs14844-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Population-based, cross-sectional study using Resident Assessment Instrument Minimum Data Set 2.0 linked to health administrative data.</p></div></div>
<div class="section" id="jgs14844-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Ontario, Canada.</p></div></div>
<div class="section" id="jgs14844-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>All 9,298 nursing home residents with advanced dementia who died between June 1, 2010, and March 31, 2013; were aged 66 and older at time of death; and received at least one MQB in their last year of life.</p></div></div>
<div class="section" id="jgs14844-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Prevalence of eight classes of MQBs (e.g., lipid-lowering agents, antidementia drugs) used in the last 120 days and last week of life.</p></div></div>
<div class="section" id="jgs14844-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Of older nursing home residents with advanced dementia who received at least one MQB in the last year of life, 8,027 (86.3%) received them in the last 120 days and 4,180 (45.0%) in the last week of life. The most commonly prescribed MQB were antidementia (63.6%) and lipid-lowering agents (47.8%). Severe cognitive impairment (adjusted odds ratio (aOR) = 1.19, 95% confidence interval (CI) = 1.07–1.33, <em>P</em> = .002) and fewer signs and symptoms of health instability (aOR = 1.58, 95% CI = 1.44–1.74, <em>P</em> &lt; .001) were associated with MQB use into the last week of life. Seeing a neurologist or psychiatrist was associated with less likelihood of MQB use in the last week of life.</p></div></div>
<div class="section" id="jgs14844-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Many nursing home residents with advanced dementia are dispensed MQBs in the last week of life. Given that MQBs may cause more harm than benefit in this vulnerable population, it is important for physicians to actively reassess the role of all medications toward the end of life.</p></div></div>
]]></content:encoded><description>

Objectives
To determine the prevalence of and resident characteristics associated with the prescription of medications of questionable benefit (MQBs) near the end of life in older adults with advanced dementia in nursing homes.


Design
Population-based, cross-sectional study using Resident Assessment Instrument Minimum Data Set 2.0 linked to health administrative data.


Setting
Ontario, Canada.


Participants
All 9,298 nursing home residents with advanced dementia who died between June 1, 2010, and March 31, 2013; were aged 66 and older at time of death; and received at least one MQB in their last year of life.


Measurements
Prevalence of eight classes of MQBs (e.g., lipid-lowering agents, antidementia drugs) used in the last 120 days and last week of life.


Results
Of older nursing home residents with advanced dementia who received at least one MQB in the last year of life, 8,027 (86.3%) received them in the last 120 days and 4,180 (45.0%) in the last week of life. The most commonly prescribed MQB were antidementia (63.6%) and lipid-lowering agents (47.8%). Severe cognitive impairment (adjusted odds ratio (aOR) = 1.19, 95% confidence interval (CI) = 1.07–1.33, P = .002) and fewer signs and symptoms of health instability (aOR = 1.58, 95% CI = 1.44–1.74, P &lt; .001) were associated with MQB use into the last week of life. Seeing a neurologist or psychiatrist was associated with less likelihood of MQB use in the last week of life.


Conclusion
Many nursing home residents with advanced dementia are dispensed MQBs in the last week of life. Given that MQBs may cause more harm than benefit in this vulnerable population, it is important for physicians to actively reassess the role of all medications toward the end of life.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14932" xmlns="http://purl.org/rss/1.0/"><title>The Physical and Cognitive Performance Test for Residents in Assisted Living Facilities</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14932</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The Physical and Cognitive Performance Test for Residents in Assisted Living Facilities</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mary Elizabeth Bowen, Meredeth Rowe, Mary Ersek, Said Ibrahim, Judy A. Shea</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-05-08T09:30:30.604749-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14932</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14932</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14932</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Brief Methodological Report</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1543</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1548</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14932-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To develop and evaluate the psychometric properties of a new performance-based instrument (Physical and Cognitive Performance Test for Assisted Living Facilities (PCPT ALF)) designed to assess the physical and cognitive skills associated with performance of activities of daily living (ADLs) and instrumental activities of daily living (IADLs).</p></div></div>
<div class="section" id="jgs14932-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>There were three stages in this study: development of instrument items and validity testing, a feasibility pilot study, and a cross-sectional trial to establish construct and criterion validity and reliability.</p></div></div>
<div class="section" id="jgs14932-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>One 116-bed assisted living facility (ALF).</p></div></div>
<div class="section" id="jgs14932-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>After a pilot test with 10 residents, a cross-sectional trial was conducted with 55 additional residents.</p></div></div>
<div class="section" id="jgs14932-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>The Barthel Index and Functional Independence Measure were used to estimate criterion validity. Construct validity was examined using exploratory factor analyses (EFAs).</p></div></div>
<div class="section" id="jgs14932-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Disattenuated correlations between the PCPT ALF and other tools were all greater than 0.72, supporting criterion validity. Internal consistency (physical ability, <em>α</em> = 0.95; cognitive support, <em>α</em> = 0.92) and 1-week test–retest reliability (PCPT ALF,<em> P</em> = .93) were high, as was interrater reliability (IRR) (physical ability, 0.99; cognitive support, 1.00). In two EFAs, a one-factor solution accounted for 64.1% of the variance for the physical ability subscale and 63.5% of the variance for the cognitive support subscale.</p></div></div>
<div class="section" id="jgs14932-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>The findings provide early evidence of the PCPT ALF's validity and reliability. If confirmed, this study's findings may be used in future work to assess the success of interventions to prevent or slow decline in the skills associated with ADL and IADL performance in ALFs.</p></div></div>
]]></content:encoded><description>

Objectives
To develop and evaluate the psychometric properties of a new performance-based instrument (Physical and Cognitive Performance Test for Assisted Living Facilities (PCPT ALF)) designed to assess the physical and cognitive skills associated with performance of activities of daily living (ADLs) and instrumental activities of daily living (IADLs).


Design
There were three stages in this study: development of instrument items and validity testing, a feasibility pilot study, and a cross-sectional trial to establish construct and criterion validity and reliability.


Setting
One 116-bed assisted living facility (ALF).


Participants
After a pilot test with 10 residents, a cross-sectional trial was conducted with 55 additional residents.


Measurements
The Barthel Index and Functional Independence Measure were used to estimate criterion validity. Construct validity was examined using exploratory factor analyses (EFAs).


Results
Disattenuated correlations between the PCPT ALF and other tools were all greater than 0.72, supporting criterion validity. Internal consistency (physical ability, α = 0.95; cognitive support, α = 0.92) and 1-week test–retest reliability (PCPT ALF, P = .93) were high, as was interrater reliability (IRR) (physical ability, 0.99; cognitive support, 1.00). In two EFAs, a one-factor solution accounted for 64.1% of the variance for the physical ability subscale and 63.5% of the variance for the cognitive support subscale.


Conclusion
The findings provide early evidence of the PCPT ALF's validity and reliability. If confirmed, this study's findings may be used in future work to assess the success of interventions to prevent or slow decline in the skills associated with ADL and IADL performance in ALFs.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14943" xmlns="http://purl.org/rss/1.0/"><title>Research Priorities to Advance the Health and Health Care of Older Adults with Multiple Chronic Conditions</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14943</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Research Priorities to Advance the Health and Health Care of Older Adults with Multiple Chronic Conditions</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mayra Tisminetzky, Elizabeth A. Bayliss, Jay S. Magaziner, Heather G. Allore, Kathryn Anzuoni, Cynthia M. Boyd, Thomas M. Gill, Alan S. Go, Susan L. Greenspan, Leah R. Hanson, Mark C. Hornbrook, Dalane W. Kitzman, Eric B. Larson, Mary D. Naylor, Benjamin E. Shirley, Ming Tai-Seale, Linda Teri, Mary E. Tinetti, Heather E. Whitson, Jerry H. Gurwitz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-05-26T14:40:31.519997-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14943</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14943</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14943</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Brief Methodological Report</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1549</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1553</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14943-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To prioritize research topics relevant to the care of the growing population of older adults with multiple chronic conditions (MCCs).</p></div></div>
<div class="section" id="jgs14943-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Survey of experts in MCC practice, research, and policy. Topics were derived from white papers, funding announcements, or funded research projects relating to older adults with MCCs.</p></div></div>
<div class="section" id="jgs14943-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Survey conducted through the Health Care Systems Research Network (HCSRN) and Claude D. Pepper Older Americans Independence Centers (OAICs) Advancing Geriatrics Infrastructure and Network Growth Initiative, a joint endeavor of the HCSRN and OAICs.</p></div></div>
<div class="section" id="jgs14943-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Individuals affiliated with the HCSRN or OAICs and national MCC experts, including individuals affiliated with funding agencies having MCC-related grant portfolios.</p></div></div>
<div class="section" id="jgs14943-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>A “top box” methodology was used, counting the number of respondents selecting the top response on a 5-point Likert scale and dividing by the total number of responses to calculate a top box percentage for each of 37 topics.</p></div></div>
<div class="section" id="jgs14943-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The highest-ranked research topics relevant to the health and healthcare of older adults with MCCs were health-related quality of life in older adults with MCCs; development of assessment tools (to assess, e.g., symptom burden, quality of life, function); interactions between medications, disease processes, and health outcomes; disability; implementation of novel (and scalable) models of care; association between clusters of chronic conditions and clinical, financial, and social outcomes; role of caregivers; symptom burden; shared decision-making to enhance care planning; and tools to improve clinical decision-making.</p></div></div>
<div class="section" id="jgs14943-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Study findings serve to inform the development of a comprehensive research agenda to address the challenges relating to the care of this “high-need, high-cost” population and the healthcare delivery systems responsible for serving it.</p></div></div>
]]></content:encoded><description>

Objectives
To prioritize research topics relevant to the care of the growing population of older adults with multiple chronic conditions (MCCs).


Design
Survey of experts in MCC practice, research, and policy. Topics were derived from white papers, funding announcements, or funded research projects relating to older adults with MCCs.


Setting
Survey conducted through the Health Care Systems Research Network (HCSRN) and Claude D. Pepper Older Americans Independence Centers (OAICs) Advancing Geriatrics Infrastructure and Network Growth Initiative, a joint endeavor of the HCSRN and OAICs.


Participants
Individuals affiliated with the HCSRN or OAICs and national MCC experts, including individuals affiliated with funding agencies having MCC-related grant portfolios.


Measurements
A “top box” methodology was used, counting the number of respondents selecting the top response on a 5-point Likert scale and dividing by the total number of responses to calculate a top box percentage for each of 37 topics.


Results
The highest-ranked research topics relevant to the health and healthcare of older adults with MCCs were health-related quality of life in older adults with MCCs; development of assessment tools (to assess, e.g., symptom burden, quality of life, function); interactions between medications, disease processes, and health outcomes; disability; implementation of novel (and scalable) models of care; association between clusters of chronic conditions and clinical, financial, and social outcomes; role of caregivers; symptom burden; shared decision-making to enhance care planning; and tools to improve clinical decision-making.


Conclusion
Study findings serve to inform the development of a comprehensive research agenda to address the challenges relating to the care of this “high-need, high-cost” population and the healthcare delivery systems responsible for serving it.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14832" xmlns="http://purl.org/rss/1.0/"><title>Oral Health and Dental Care in Older Asian Americans in Central Texas</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14832</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Oral Health and Dental Care in Older Asian Americans in Central Texas</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yuri Jang, Hyunwoo Yoon, Nan Sook Park, David A. Chiriboga</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-05-26T14:40:24.52928-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14832</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14832</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14832</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Brief Report</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1554</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1558</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14832-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To examine factors associated with dental health insurance, self-rated oral health, and use of preventive dental care services in older Asian Americans.</p></div></div>
<div class="section" id="jgs14832-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Cross-sectional survey.</p></div></div>
<div class="section" id="jgs14832-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>The Asian American Quality of Life Survey was conducted with 2,614 Asian Americans living in central Texas using questionnaires available in English and six Asian languages.</p></div></div>
<div class="section" id="jgs14832-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Asian American Quality of Life Survey participants aged 60 and older (N = 533; mean age = 69.4 ± 6.9).</p></div></div>
<div class="section" id="jgs14832-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Participants were asked whether they had insurance that covered the cost of any dental visit, how they would rate their overall oral health status, and whether they had visited a dental clinic for a routine examination in the past 12 months. Information was also collected on sociodemographic and immigration-related variables.</p></div></div>
<div class="section" id="jgs14832-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>More than 61% of the sample had no dental health insurance, 45% reported that their oral health was fair or poor, and 44% had not used preventive dental care services. A series of logistic regression analyses identified factors posing a significant risk to oral health and dental care. For example, those with limited English proficiency were 3.5 times as likely to lack dental health insurance and 3.2 times as likely to rate their oral health as fair or poor. The odds of not using preventive dental care services were 6.4 times as great in those without dental health insurance.</p></div></div>
<div class="section" id="jgs14832-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>The overall findings call attention to efforts to promote oral health and dental care in older Asian Americans.</p></div></div>
]]></content:encoded><description>

Objectives
To examine factors associated with dental health insurance, self-rated oral health, and use of preventive dental care services in older Asian Americans.


Design
Cross-sectional survey.


Setting
The Asian American Quality of Life Survey was conducted with 2,614 Asian Americans living in central Texas using questionnaires available in English and six Asian languages.


Participants
Asian American Quality of Life Survey participants aged 60 and older (N = 533; mean age = 69.4 ± 6.9).


Measurements
Participants were asked whether they had insurance that covered the cost of any dental visit, how they would rate their overall oral health status, and whether they had visited a dental clinic for a routine examination in the past 12 months. Information was also collected on sociodemographic and immigration-related variables.


Results
More than 61% of the sample had no dental health insurance, 45% reported that their oral health was fair or poor, and 44% had not used preventive dental care services. A series of logistic regression analyses identified factors posing a significant risk to oral health and dental care. For example, those with limited English proficiency were 3.5 times as likely to lack dental health insurance and 3.2 times as likely to rate their oral health as fair or poor. The odds of not using preventive dental care services were 6.4 times as great in those without dental health insurance.


Conclusion
The overall findings call attention to efforts to promote oral health and dental care in older Asian Americans.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14846" xmlns="http://purl.org/rss/1.0/"><title>Comprehensive Geriatric Assessment for Prevention of Delirium After Hip Fracture: A Systematic Review of Randomized Controlled Trials</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14846</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comprehensive Geriatric Assessment for Prevention of Delirium After Hip Fracture: A Systematic Review of Randomized Controlled Trials</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lynn Shields, Victoria Henderson, Robert Caslake</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-04-13T11:32:24.319487-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14846</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14846</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14846</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Brief Report</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1559</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1565</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14846-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To assess the efficacy of comprehensive geriatric assessment (CGA) in prevention of delirium after hip fracture.</p></div></div>
<div class="section" id="jgs14846-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Systematic review and metaanalysis.</p></div></div>
<div class="section" id="jgs14846-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Ward based models on geriatrics wards and visiting team based models on orthopaedics wards were included.</p></div></div>
<div class="section" id="jgs14846-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Four trials (three European, one U.S.; 973 participants) were identified. Two assessed ward-based, and two assessed team-based interventions.</p></div></div>
<div class="section" id="jgs14846-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>MEDLINE, EMBASE, CINAHL and PsycINFO databases; Clinicaltrials.gov; and the Central Register of Controlled Trials were searched. Reference lists from full-text articles were reviewed. Incidence of delirium was the primary outcome. Length of stay, delirium severity, institutionalization, long-term cognition and mortality were predefined secondary outcomes. Duration of delirium was included as a post hoc outcome.</p></div></div>
<div class="section" id="jgs14846-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>There was a significant reduction in delirium overall (relative risk (RR) = 0.81, 95% confidence interval (CI) = 0.69–0.94) in the intervention group. Post hoc subgroup analysis found this effect to be preserved in the team-based intervention group (RR = 0.77, 95% CI = 0.61–0.98) but not the ward-based group. No significant effect was observed on any secondary outcome.</p></div></div>
<div class="section" id="jgs14846-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>There was a reduction in the incidence of delirium after hip fracture with CGA. This is in keeping with results of non-randomized controlled trials and trials in other populations. Team-based interventions appeared superior in contrast to the Ellis CGA paper, but it is likely that heterogeneity in interventions and population studied affected this.</p></div></div>
]]></content:encoded><description>

Objectives
To assess the efficacy of comprehensive geriatric assessment (CGA) in prevention of delirium after hip fracture.


Design
Systematic review and metaanalysis.


Setting
Ward based models on geriatrics wards and visiting team based models on orthopaedics wards were included.


Participants
Four trials (three European, one U.S.; 973 participants) were identified. Two assessed ward-based, and two assessed team-based interventions.


Measurements
MEDLINE, EMBASE, CINAHL and PsycINFO databases; Clinicaltrials.gov; and the Central Register of Controlled Trials were searched. Reference lists from full-text articles were reviewed. Incidence of delirium was the primary outcome. Length of stay, delirium severity, institutionalization, long-term cognition and mortality were predefined secondary outcomes. Duration of delirium was included as a post hoc outcome.


Results
There was a significant reduction in delirium overall (relative risk (RR) = 0.81, 95% confidence interval (CI) = 0.69–0.94) in the intervention group. Post hoc subgroup analysis found this effect to be preserved in the team-based intervention group (RR = 0.77, 95% CI = 0.61–0.98) but not the ward-based group. No significant effect was observed on any secondary outcome.


Conclusion
There was a reduction in the incidence of delirium after hip fracture with CGA. This is in keeping with results of non-randomized controlled trials and trials in other populations. Team-based interventions appeared superior in contrast to the Ellis CGA paper, but it is likely that heterogeneity in interventions and population studied affected this.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14840" xmlns="http://purl.org/rss/1.0/"><title>Ageism in Studies on the Management of Osteoporosis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14840</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ageism in Studies on the Management of Osteoporosis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Caoimhe McGarvey, Tara Coughlan, Desmond O'Neill</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-06T10:40:33.140235-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14840</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14840</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14840</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Brief Report</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1566</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1568</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14840-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To review the literature to assess whether the fact that osteoporosis is chiefly considered a disease of the older population was reflected in research in the area of the management of osteoporosis and to determine the extent of ageism in studies on the management of osteoporosis.</p></div></div>
<div class="section" id="jgs14840-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Review.</p></div></div>
<div class="section" id="jgs14840-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>All randomized control trials on the management of osteoporosis entered in the Cochrane Library Database that reported mean age were included. Exclusion criteria were also examined. Of 284 randomized control trials identified, 102 were eligible for inclusion.</p></div></div>
<div class="section" id="jgs14840-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Older adult trail participants.</p></div></div>
<div class="section" id="jgs14840-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Mean age of participants and exclusion criteria used were analyzed.</p></div></div>
<div class="section" id="jgs14840-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>The mean age of all participants was 64.0, despite the fact that the average age at hip fracture is 83 for women and 84 for men. Overall, the mean age of those presenting with hip fractures is 84.8. Twenty-four (23%) of the 102 trials used older age as an exclusion factor. Other exclusion factors were long time since menopause, impaired cardiac or pulmonary function, dependent in ambulation, any severe comorbidity, dementia or any cognitive impairment, recent history of peptic ulcer disease or erosive gastric disease, uncontrolled hypertension, and psychiatric illness.</p></div></div>
<div class="section" id="jgs14840-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>These data show a distinct difference between the mean age of participants in studies of the management of osteoporosis and the mean age of those presenting with hip fractures. Given that osteoporosis is the leading cause of hip fractures, this finding could have a significant effect on future studies in this area. It would follow that future research should include a cohort of an age that is more reflective of those most likely to experience the adverse effects of osteoporosis.</p></div></div>
]]></content:encoded><description>

Objectives
To review the literature to assess whether the fact that osteoporosis is chiefly considered a disease of the older population was reflected in research in the area of the management of osteoporosis and to determine the extent of ageism in studies on the management of osteoporosis.


Design
Review.


Setting
All randomized control trials on the management of osteoporosis entered in the Cochrane Library Database that reported mean age were included. Exclusion criteria were also examined. Of 284 randomized control trials identified, 102 were eligible for inclusion.


Participants
Older adult trail participants.


Measurements
Mean age of participants and exclusion criteria used were analyzed.


Results
The mean age of all participants was 64.0, despite the fact that the average age at hip fracture is 83 for women and 84 for men. Overall, the mean age of those presenting with hip fractures is 84.8. Twenty-four (23%) of the 102 trials used older age as an exclusion factor. Other exclusion factors were long time since menopause, impaired cardiac or pulmonary function, dependent in ambulation, any severe comorbidity, dementia or any cognitive impairment, recent history of peptic ulcer disease or erosive gastric disease, uncontrolled hypertension, and psychiatric illness.


Conclusion
These data show a distinct difference between the mean age of participants in studies of the management of osteoporosis and the mean age of those presenting with hip fractures. Given that osteoporosis is the leading cause of hip fractures, this finding could have a significant effect on future studies in this area. It would follow that future research should include a cohort of an age that is more reflective of those most likely to experience the adverse effects of osteoporosis.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14865" xmlns="http://purl.org/rss/1.0/"><title>Psychiatric Diagnoses Among Older Recipients of Publicly Funded Mental Health Services</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14865</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Psychiatric Diagnoses Among Older Recipients of Publicly Funded Mental Health Services</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sarah T. Stahl, Charles F. Reynolds, Ellen M. Whyte, Steven M. Albert</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-17T10:20:23.333148-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14865</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14865</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14865</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Brief Report</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1569</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1572</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14865-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To compare the prevalence of psychiatric diagnoses among older recipients of publicly funded mental health services (county safety-net base services and Medicaid) to psychiatric diagnoses in an insured population of older adults from the same county.</p></div></div>
<div class="section" id="jgs14865-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Secondary analysis of county human services claims data and claims from an insured population in the same county.</p></div></div>
<div class="section" id="jgs14865-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Inpatient and outpatient clinics in Allegheny County, PA.</p></div></div>
<div class="section" id="jgs14865-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Adults aged 65 and older in the county who received treatment for a psychiatric diagnosis in 2012 (county base services, n = 1,457; Medicaid, n = 641; Health plan insurance, n = 5,595).</p></div></div>
<div class="section" id="jgs14865-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Psychiatric diagnoses were classified using the International Classification of Diseases, 9th revision (ICD-9).</p></div></div>
<div class="section" id="jgs14865-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Episodic mood disorders and schizophrenia were more common among county-funded and Medicaid recipients (50–54% vs 34%). Neurotic conditions were more common among older adults with health plan insurance (18% vs 8%). Nearly a quarter of older adults receiving county base services were classified as having “ill-defined and unknown causes of morbidity and mortality,” compared &lt;1% among insured and 6% among Medicaid recipients.</p></div></div>
<div class="section" id="jgs14865-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusions</h4><div class="para"><p>The prevalence of psychiatric conditions among older adults varies by insurance coverage, suggesting a role for social and economic factors associated with safety net coverage as well as system-level differences in delivery of mental health services. Comparing the prevalence of psychiatric diagnoses across insurance types offers insight on social determinants of risk for mental disorders in late life.</p></div></div>
]]></content:encoded><description>

Objectives
To compare the prevalence of psychiatric diagnoses among older recipients of publicly funded mental health services (county safety-net base services and Medicaid) to psychiatric diagnoses in an insured population of older adults from the same county.


Design
Secondary analysis of county human services claims data and claims from an insured population in the same county.


Setting
Inpatient and outpatient clinics in Allegheny County, PA.


Participants
Adults aged 65 and older in the county who received treatment for a psychiatric diagnosis in 2012 (county base services, n = 1,457; Medicaid, n = 641; Health plan insurance, n = 5,595).


Measurements
Psychiatric diagnoses were classified using the International Classification of Diseases, 9th revision (ICD-9).


Results
Episodic mood disorders and schizophrenia were more common among county-funded and Medicaid recipients (50–54% vs 34%). Neurotic conditions were more common among older adults with health plan insurance (18% vs 8%). Nearly a quarter of older adults receiving county base services were classified as having “ill-defined and unknown causes of morbidity and mortality,” compared &lt;1% among insured and 6% among Medicaid recipients.


Conclusions
The prevalence of psychiatric conditions among older adults varies by insurance coverage, suggesting a role for social and economic factors associated with safety net coverage as well as system-level differences in delivery of mental health services. Comparing the prevalence of psychiatric diagnoses across insurance types offers insight on social determinants of risk for mental disorders in late life.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14879" xmlns="http://purl.org/rss/1.0/"><title>Do-Not-Hospitalize Orders in Nursing Homes: “Call the Family Instead of Calling the Ambulance”</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14879</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Do-Not-Hospitalize Orders in Nursing Homes: “Call the Family Instead of Calling the Ambulance”</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Andrew B. Cohen, M. Tish Knobf, Terri R. Fried</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-30T07:26:57.011256-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14879</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14879</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14879</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Brief Report</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1573</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1577</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14879-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To determine how do-not-hospitalize (DNH) orders are interpreted and used in nursing homes (NHs) once they are in place.</p></div></div>
<div class="section" id="jgs14879-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Qualitative study using in-depth semi-structured interviews performed from December 2013 to April 2014.</p></div></div>
<div class="section" id="jgs14879-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Eight skilled nursing facilities in Connecticut that ranked in the top 10% or bottom 10% in hospitalization rates from 2008 to 2010.</p></div></div>
<div class="section" id="jgs14879-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Nursing facility staff members (N = 31).</p></div></div>
<div class="section" id="jgs14879-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>A multidisciplinary team performed qualitative content analysis. The constant comparative method was used to develop a coding structure and identify themes.</p></div></div>
<div class="section" id="jgs14879-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>DNH orders were uncommon at low- and high-hospitalizing facilities. Participants reported that they did not interpret these orders literally. A DNH order was not a prohibition against hospitalization but was understood to have a variety of exceptions. These orders functioned primarily as a signal that hospitalization should be questioned and discussed with the family when an acute event occurred.</p></div></div>
<div class="section" id="jgs14879-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>In-the-moment discussions about hospitalization are still necessary even when a DNH order is in place. Work to reduce potentially burdensome NH–hospital transfers needs to focus not just on eliciting preferences in advance, but also on preparing residents and their families to make the best decisions about hospitalization when the time comes.</p></div></div>
]]></content:encoded><description>

Objectives
To determine how do-not-hospitalize (DNH) orders are interpreted and used in nursing homes (NHs) once they are in place.


Design
Qualitative study using in-depth semi-structured interviews performed from December 2013 to April 2014.


Setting
Eight skilled nursing facilities in Connecticut that ranked in the top 10% or bottom 10% in hospitalization rates from 2008 to 2010.


Participants
Nursing facility staff members (N = 31).


Measurements
A multidisciplinary team performed qualitative content analysis. The constant comparative method was used to develop a coding structure and identify themes.


Results
DNH orders were uncommon at low- and high-hospitalizing facilities. Participants reported that they did not interpret these orders literally. A DNH order was not a prohibition against hospitalization but was understood to have a variety of exceptions. These orders functioned primarily as a signal that hospitalization should be questioned and discussed with the family when an acute event occurred.


Conclusion
In-the-moment discussions about hospitalization are still necessary even when a DNH order is in place. Work to reduce potentially burdensome NH–hospital transfers needs to focus not just on eliciting preferences in advance, but also on preparing residents and their families to make the best decisions about hospitalization when the time comes.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14870" xmlns="http://purl.org/rss/1.0/"><title>Common Drug Side Effects and Drug-Drug Interactions in Elderly Adults in Primary Care</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14870</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Common Drug Side Effects and Drug-Drug Interactions in Elderly Adults in Primary Care</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Susan E. Merel, Douglas S. Paauw</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-21T23:01:55.934094-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14870</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14870</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14870</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Clinical Management of the Older Adult</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1578</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1585</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Prescribing medications, recognizing and managing medication side effects and drug interactions, and avoiding polypharmacy are all essential skills in the care of older adults in primary care. Important side effects of medications commonly prescribed in older adults (statins, proton pump inhibitors, trimethoprim-sulfamethoxazole and fluoroquinolone antibiotics, zolpidem, nonsteroidal antiinflammatory drugs, selective serotonin reuptake inhibitors, dipeptidyl peptidase 4 inhibitors) were reviewed. Important drug interactions with four agents or classes (statins, warfarin, factor Xa inhibitors, and calcium channel blockers) are discussed.</p></div>
]]></content:encoded><description>
Prescribing medications, recognizing and managing medication side effects and drug interactions, and avoiding polypharmacy are all essential skills in the care of older adults in primary care. Important side effects of medications commonly prescribed in older adults (statins, proton pump inhibitors, trimethoprim-sulfamethoxazole and fluoroquinolone antibiotics, zolpidem, nonsteroidal antiinflammatory drugs, selective serotonin reuptake inhibitors, dipeptidyl peptidase 4 inhibitors) were reviewed. Important drug interactions with four agents or classes (statins, warfarin, factor Xa inhibitors, and calcium channel blockers) are discussed.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14815" xmlns="http://purl.org/rss/1.0/"><title>Oral and Maxillofacial Lesions Diagnosed in Older People of a Brazilian Population: A Multicentric Study</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14815</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Oral and Maxillofacial Lesions Diagnosed in Older People of a Brazilian Population: A Multicentric Study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Leorik P. Silva, Rafaella B. Leite, Ana P. V. Sobral, José A. Arruda, Leni V. Oliveira, Mariana S. Noronha, Camila O. Kato, Ricardo A. Mesquita, Lauren F. Schuch, Ana P. N. Gomes, Ana C. U. Vasconcelos, Lélia B. Souza</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-13T10:20:25.941363-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14815</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14815</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14815</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Dental and Oral Health</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1586</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1590</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14815-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>The aim of this study was to investigate the prevalence of oral and maxillofacial lesions among older adults (≥60 years) from representative regions in Brazil.</p></div></div>
<div class="section" id="jgs14815-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Retrospective descriptive cross-sectional study.</p></div></div>
<div class="section" id="jgs14815-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>Biopsy records were obtained from the archives of four Brazilian referral centers of oral diagnosis between 2000 and 2016.</p></div></div>
<div class="section" id="jgs14815-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>A total of 45,506 biopsy records of all patients were analyzed, of these 7,259 persons aged 60 and older were selected.</p></div></div>
<div class="section" id="jgs14815-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Data such as gender, age, race, anatomical location, and histopathological diagnosis were collected and categorized. Pearson's chi-square test (<em>P</em> &lt; .005) was used to evaluate differences in the frequency of the several groups of oral lesions.</p></div></div>
<div class="section" id="jgs14815-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Oral and maxillofacial lesions were diagnosed in 7,259 older people, including 59.4% women (<em>P</em> &lt; .001) and 61.3% white patients (<em>P</em> = .07). The most commonly affected sites were the cheek mucosa (20.3%) and mandible (8.9%) (<em>P</em> &lt; .001). Reactive and inflammatory lesions were the most common lesions, followed by neoplasms. Oral squamous cell carcinoma was the most prevalent neoplasm (83.4%) (<em>P</em> &lt; .001).</p></div></div>
<div class="section" id="jgs14815-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>Knowledge of oral diseases obtained from biopsy records provides more accurate data about the diagnosis and oral health of elderly patients. These indicators thus support the development of specific health policies for the prevention and treatment of oral and maxillofacial lesions that affect this population.</p></div></div>
]]></content:encoded><description>

Objectives
The aim of this study was to investigate the prevalence of oral and maxillofacial lesions among older adults (≥60 years) from representative regions in Brazil.


Design
Retrospective descriptive cross-sectional study.


Setting
Biopsy records were obtained from the archives of four Brazilian referral centers of oral diagnosis between 2000 and 2016.


Participants
A total of 45,506 biopsy records of all patients were analyzed, of these 7,259 persons aged 60 and older were selected.


Measurements
Data such as gender, age, race, anatomical location, and histopathological diagnosis were collected and categorized. Pearson's chi-square test (P &lt; .005) was used to evaluate differences in the frequency of the several groups of oral lesions.


Results
Oral and maxillofacial lesions were diagnosed in 7,259 older people, including 59.4% women (P &lt; .001) and 61.3% white patients (P = .07). The most commonly affected sites were the cheek mucosa (20.3%) and mandible (8.9%) (P &lt; .001). Reactive and inflammatory lesions were the most common lesions, followed by neoplasms. Oral squamous cell carcinoma was the most prevalent neoplasm (83.4%) (P &lt; .001).


Conclusion
Knowledge of oral diseases obtained from biopsy records provides more accurate data about the diagnosis and oral health of elderly patients. These indicators thus support the development of specific health policies for the prevention and treatment of oral and maxillofacial lesions that affect this population.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14875" xmlns="http://purl.org/rss/1.0/"><title>Age of Migration Life Expectancy with Functional Limitations and Morbidity in Mexican Americans</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14875</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Age of Migration Life Expectancy with Functional Limitations and Morbidity in Mexican Americans</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marc A. Garcia, Luis M. Valderrama-Hinds, Chi-Tsun Chiu, Miriam S. Mutambudzi, Nai-Wei Chen, Mukaila Raji</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-30T07:26:55.265908-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14875</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14875</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14875</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Ethnogeriatrics and Special Populations</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1591</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1596</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14875-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><div class="para"><p>The U.S. Mexican American population enjoys longer life expectancies relative to other racial/ethnic groups but is disproportionately affected by chronic conditions and functional limitations. Studying the impact of heterogeneity in age, time and other characteristics of migration among older Mexican Americans can inform our understanding of health disparities and healthcare needs in later-life. This research used 20 years of data from the Hispanic Established Populations for the Epidemiologic Study of the Elderly to assess the proportion of life spent with functional limitations and one or more morbidity (according to age of migration and sex) in the U.S. Mexican-American population. The results indicate that early-life and late-life migrant women spend more years with Performance-Oriented Mobility Assessment limitations than U.S.-born women. Conversely, midlife migrant women were not statistically different from U.S.-born women in years spent disabled. In men, midlife migrants had longer life expectancies and had more disability-free years than U.S.-born men. For morbidity, late-life migrant women spent a significantly smaller proportion of their elderly years with morbidity than U.S.-born women, but late-life migrant men spent more years with morbidity than U.S.-born men. These findings illustrate that older Mexican Americans in the United States are heterogeneous in nativity and health outcomes. More years spent disabled or unhealthy may result in greater burden on family members and greater dependence on public resources. These findings have implications for the development of social and health policies to appropriately target the medical conditions and disabilities of older Mexican Americans entering late life.</p></div></div>
]]></content:encoded><description>

The U.S. Mexican American population enjoys longer life expectancies relative to other racial/ethnic groups but is disproportionately affected by chronic conditions and functional limitations. Studying the impact of heterogeneity in age, time and other characteristics of migration among older Mexican Americans can inform our understanding of health disparities and healthcare needs in later-life. This research used 20 years of data from the Hispanic Established Populations for the Epidemiologic Study of the Elderly to assess the proportion of life spent with functional limitations and one or more morbidity (according to age of migration and sex) in the U.S. Mexican-American population. The results indicate that early-life and late-life migrant women spend more years with Performance-Oriented Mobility Assessment limitations than U.S.-born women. Conversely, midlife migrant women were not statistically different from U.S.-born women in years spent disabled. In men, midlife migrants had longer life expectancies and had more disability-free years than U.S.-born men. For morbidity, late-life migrant women spent a significantly smaller proportion of their elderly years with morbidity than U.S.-born women, but late-life migrant men spent more years with morbidity than U.S.-born men. These findings illustrate that older Mexican Americans in the United States are heterogeneous in nativity and health outcomes. More years spent disabled or unhealthy may result in greater burden on family members and greater dependence on public resources. These findings have implications for the development of social and health policies to appropriately target the medical conditions and disabilities of older Mexican Americans entering late life.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14828" xmlns="http://purl.org/rss/1.0/"><title>Impact of Transitional Care Services for Chronically Ill Older Patients: A Systematic Evidence Review</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14828</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Impact of Transitional Care Services for Chronically Ill Older Patients: A Systematic Evidence Review</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mélanie Le Berre, Geva Maimon, Nadia Sourial, Muriel Guériton, Isabelle Vedel</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-04-12T12:53:06.500237-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14828</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14828</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14828</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Models of Geriatric Care, Quality Improvement, and Program Dissemination</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1597</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1608</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>Transitions in care from hospital to primary care for older patients with chronic diseases (CD) are complex and lead to increased mortality and service use. In response to these challenges, transitional care (TC) interventions are being widely implemented. They encompass education on self-management, discharge planning, structured follow-up and coordination among the different healthcare professionals. We conducted a systematic review to determine the effectiveness of interventions targeting transitions from hospital to the primary care setting for chronically ill older patients.. Randomized controlled trials were identified through Medline, CINHAL, PsycInfo, EMBASE (1995–2015). Two independent reviewers performed the study selection, data extraction and assessment of study quality (Cochrane “Risk of Bias”). Risk differences (RD) and number needed to treat (NNT) or mean differences (MD) were calculated using a random-effects model. From 10,234 references, 92 studies were included. Compared to usual care, significantly better outcomes were observed: a lower mortality at 3 (RD: −0.02 [−0.05, 0.00]; NNT: 50), 6, 12 and 18 months post-discharge, a lower rate of ED visits at 3 months (RD: −0.08 [−0.15, −0.01]; NNT: 13), a lower rate of readmissions at 3 (RD: −0.08 [−0.14, −0.03]; NNT: 7), 6, 12 and 18 months and a lower mean of readmission days at 3 (MD: −1.33; [−2.15, −0.52]), 6, 12 and 18 months. No significant differences were observed in quality of life. In conclusion, TC improves transitions for older patients and should be included in the reorganization of healthcare services.</p></div>
]]></content:encoded><description>
Transitions in care from hospital to primary care for older patients with chronic diseases (CD) are complex and lead to increased mortality and service use. In response to these challenges, transitional care (TC) interventions are being widely implemented. They encompass education on self-management, discharge planning, structured follow-up and coordination among the different healthcare professionals. We conducted a systematic review to determine the effectiveness of interventions targeting transitions from hospital to the primary care setting for chronically ill older patients.. Randomized controlled trials were identified through Medline, CINHAL, PsycInfo, EMBASE (1995–2015). Two independent reviewers performed the study selection, data extraction and assessment of study quality (Cochrane “Risk of Bias”). Risk differences (RD) and number needed to treat (NNT) or mean differences (MD) were calculated using a random-effects model. From 10,234 references, 92 studies were included. Compared to usual care, significantly better outcomes were observed: a lower mortality at 3 (RD: −0.02 [−0.05, 0.00]; NNT: 50), 6, 12 and 18 months post-discharge, a lower rate of ED visits at 3 months (RD: −0.08 [−0.15, −0.01]; NNT: 13), a lower rate of readmissions at 3 (RD: −0.08 [−0.14, −0.03]; NNT: 7), 6, 12 and 18 months and a lower mean of readmission days at 3 (MD: −1.33; [−2.15, −0.52]), 6, 12 and 18 months. No significant differences were observed in quality of life. In conclusion, TC improves transitions for older patients and should be included in the reorganization of healthcare services.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14890" xmlns="http://purl.org/rss/1.0/"><title>Enhancing Quality of Provider Practices for Older Adults in the Emergency Department (EQUiPPED)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14890</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Enhancing Quality of Provider Practices for Older Adults in the Emergency Department (EQUiPPED)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Melissa Stevens, Susan N. Hastings, Alayne D. Markland, Ula Hwang, William Hung, Ann E. Vandenberg, William Bryan, Dewayne Cross, James Powers, Gerald McGwin, Noor Fattouh, William Ho, Carolyn Clevenger, Camille P. Vaughan</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-04-07T11:00:32.56748-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14890</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14890</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14890</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Models of Geriatric Care, Quality Improvement, and Program Dissemination</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1609</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1614</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>EQUiPPED is a multicomponent quality improvement initiative combining education, electronic clinical decision support, and individual provider feedback to influence prescribing and improve medication safety for older adults. The objective here was to evaluate the effectiveness and sustainability of EQUiPPED to reduce the use of potentially inappropriate medications (PIMs), as defined by the American Geriatrics Society 2012 Beers Criteria, prescribed to older Veterans at the time of emergency department (ED) discharge. This evaluation represents a pre- and post-intervention comparison of PIM prescriptions at 4 urban Veteran Affairs (VA) Medical Center EDs. Poisson regression was used to compare the number of PIMs prescribed to Veterans 65 years or older discharged from the ED for at least 6 months prior to the first EQUiPPED intervention at each site and for at least 12 months following the final EQUiPPED intervention. The implementation timeline varied by site depending on local resources. All 4 sites showed a significant and sustained reduction in use of PIMs. The proportion of PIMs at site one decreased from 11.9% (SD 1.8) pre-EQUiPPED to 5.1% (SD 1.4) post-EQUiPPED (<em>P</em> &lt; .0001); site 2 from 8.2% (SD 0.8) pre to 4.5% (SD 1.0) post (<em>P</em> &lt; .0001); site 3 from 8.9% (SD 1.9) pre to 6.1% (SD 1.7) post (<em>P</em> = .0007); and site 4 from 7.4% (SD 1.7) pre to 5.7% (SD 0.8) post (<em>P</em> = .04). These results suggest a multicomponent program to influence provider prescribing behavior leads to safer prescribing for older adults discharged from the ED and is sustainable across multiple VA ED sites.</p></div>
]]></content:encoded><description>
EQUiPPED is a multicomponent quality improvement initiative combining education, electronic clinical decision support, and individual provider feedback to influence prescribing and improve medication safety for older adults. The objective here was to evaluate the effectiveness and sustainability of EQUiPPED to reduce the use of potentially inappropriate medications (PIMs), as defined by the American Geriatrics Society 2012 Beers Criteria, prescribed to older Veterans at the time of emergency department (ED) discharge. This evaluation represents a pre- and post-intervention comparison of PIM prescriptions at 4 urban Veteran Affairs (VA) Medical Center EDs. Poisson regression was used to compare the number of PIMs prescribed to Veterans 65 years or older discharged from the ED for at least 6 months prior to the first EQUiPPED intervention at each site and for at least 12 months following the final EQUiPPED intervention. The implementation timeline varied by site depending on local resources. All 4 sites showed a significant and sustained reduction in use of PIMs. The proportion of PIMs at site one decreased from 11.9% (SD 1.8) pre-EQUiPPED to 5.1% (SD 1.4) post-EQUiPPED (P &lt; .0001); site 2 from 8.2% (SD 0.8) pre to 4.5% (SD 1.0) post (P &lt; .0001); site 3 from 8.9% (SD 1.9) pre to 6.1% (SD 1.7) post (P = .0007); and site 4 from 7.4% (SD 1.7) pre to 5.7% (SD 0.8) post (P = .04). These results suggest a multicomponent program to influence provider prescribing behavior leads to safer prescribing for older adults discharged from the ED and is sustainable across multiple VA ED sites.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14939" xmlns="http://purl.org/rss/1.0/"><title>Beyond the Individual: The Interdependence of Advance Directive Completion by Older Married Adults</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14939</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Beyond the Individual: The Interdependence of Advance Directive Completion by Older Married Adults</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Catheryn S. Koss</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-05-29T01:01:02.450383-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14939</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14939</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14939</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Palliative Care and Geriatrics</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1615</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1620</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<div class="section" id="jgs14939-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h4>Objectives</h4><div class="para"><p>To determine how individual and spousal demographic and health factors are associated with advance directive (AD) completion by married older adults.</p></div></div>
<div class="section" id="jgs14939-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h4>Design</h4><div class="para"><p>Dyadic structural equation modeling using the Actor-Partner Interdependence Model.</p></div></div>
<div class="section" id="jgs14939-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h4>Setting</h4><div class="para"><p>The 2004 to 2012 waves of the Health and Retirement Study.</p></div></div>
<div class="section" id="jgs14939-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h4>Participants</h4><div class="para"><p>Community-dwelling heterosexual married couples aged 65 and older (N = 2,243).</p></div></div>
<div class="section" id="jgs14939-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h4>Measurements</h4><div class="para"><p>Structural equation modeling with a probit link function was used to estimate associations between men's and women's age, education, health status, prior hospitalization or outpatient surgery in the past 10 years, regular health care provider, and household net assets and their own and their spouses’ probabilities of having an AD.</p></div></div>
<div class="section" id="jgs14939-sec-0006" xmlns="http://www.w3.org/1999/xhtml"><h4>Results</h4><div class="para"><p>Individual and spousal ages were each positively associated with AD completion for men and women. Those with higher education were more likely to possess ADs. Women's probabilities of having ADs were also positively associated with husbands’ education. Men whose wives’ were in poor health were less likely to have ADs. Men who were hospitalized or underwent outpatient surgery were more likely to have ADs, as were their wives. Women who had regular sources of health care were more likely to have completed ADs.</p></div></div>
<div class="section" id="jgs14939-sec-0007" xmlns="http://www.w3.org/1999/xhtml"><h4>Conclusion</h4><div class="para"><p>AD completion by older married adults is associated with both individual and spousal factors. How spouses influence one another's advance care planning differs by gender. Future research should account for the dyadic nature of advance care planning, as should public education efforts and interventions promoting AD completion.</p></div></div>
]]></content:encoded><description>

Objectives
To determine how individual and spousal demographic and health factors are associated with advance directive (AD) completion by married older adults.


Design
Dyadic structural equation modeling using the Actor-Partner Interdependence Model.


Setting
The 2004 to 2012 waves of the Health and Retirement Study.


Participants
Community-dwelling heterosexual married couples aged 65 and older (N = 2,243).


Measurements
Structural equation modeling with a probit link function was used to estimate associations between men's and women's age, education, health status, prior hospitalization or outpatient surgery in the past 10 years, regular health care provider, and household net assets and their own and their spouses’ probabilities of having an AD.


Results
Individual and spousal ages were each positively associated with AD completion for men and women. Those with higher education were more likely to possess ADs. Women's probabilities of having ADs were also positively associated with husbands’ education. Men whose wives’ were in poor health were less likely to have ADs. Men who were hospitalized or underwent outpatient surgery were more likely to have ADs, as were their wives. Women who had regular sources of health care were more likely to have completed ADs.


Conclusion
AD completion by older married adults is associated with both individual and spousal factors. How spouses influence one another's advance care planning differs by gender. Future research should account for the dyadic nature of advance care planning, as should public education efforts and interventions promoting AD completion.

</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14886" xmlns="http://purl.org/rss/1.0/"><title>Pioneers in Geriatrics – Passing It On</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14886</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Pioneers in Geriatrics – Passing It On</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Leo M. Cooney</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-05-08T09:25:58.729469-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14886</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14886</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14886</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Perspectives of Geriatrics by Pioneers in Aging</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1621</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1625</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14945" xmlns="http://purl.org/rss/1.0/"><title>Old and Alone</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14945</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Old and Alone</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Paul Rousseau</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-05-19T10:20:45.509375-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14945</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14945</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14945</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Old Lives Tale</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1626</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1626</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14864" xmlns="http://purl.org/rss/1.0/"><title>Healing as a Team</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14864</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Healing as a Team</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Paolo Mazzola, Domenico Picone</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-21T10:30:39.080432-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14864</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14864</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14864</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1627</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1627</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14850" xmlns="http://purl.org/rss/1.0/"><title>Comment on Effect of Resting Heart Rate on All-Cause Mortality and Cardiovascular Events According to Age</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14850</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comment on Effect of Resting Heart Rate on All-Cause Mortality and Cardiovascular Events According to Age</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Reza Pakzad, Saeid Safiri</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-13T10:30:34.073479-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14850</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14850</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14850</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1627</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1628</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14866" xmlns="http://purl.org/rss/1.0/"><title>Reply to Comment on Effect of Resting Heart Rate on All-Cause Mortality and Cardiovascular Events According to Age</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14866</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Reply to Comment on Effect of Resting Heart Rate on All-Cause Mortality and Cardiovascular Events According to Age</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kuibao Li, Chonghua Yao, Xinchun Yang, Lei Dong</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-03-13T10:30:30.164121-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14866</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14866</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14866</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1628</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1629</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14885" xmlns="http://purl.org/rss/1.0/"><title>Vitamin D for Healthy Aging</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14885</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Vitamin D for Healthy Aging</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Javier S. Morales, Nuria Garatachea, Helios Pareja-Galeano</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-04-13T06:25:25.745488-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14885</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14885</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14885</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1629</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1630</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15006" xmlns="http://purl.org/rss/1.0/"><title>Erratum</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15006</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Erratum</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-12T06:32:35.464212-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.15006</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.15006</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.15006</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Erratum</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1631</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1632</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14626" xmlns="http://purl.org/rss/1.0/"><title>Notices</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14626</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Notices</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2017-07-12T06:32:28.413407-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/jgs.14626</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/jgs.14626</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fjgs.14626</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notices</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1633</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1634</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item></rdf:RDF>