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            type="text/xsl"?><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)1748-5827" xmlns="http://purl.org/rss/1.0/"><title>Journal of Small Animal Practice</title><description> Wiley Online Library : Journal of Small Animal Practice</description><link>http://dx.doi.org/10.1111%2F%28ISSN%291748-5827</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/">© British Small Animal Veterinary Association</dc:rights><prism:issn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">0022-4510</prism:issn><prism:eIssn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1748-5827</prism:eIssn><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><prism:coverDisplayDate xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">February 2012</prism:coverDisplayDate><prism:volume xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">53</prism:volume><prism:number xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">2</prism:number><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">87</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">143</prism:endingPage><image rdf:resource="http://onlinelibrary.wiley.com/store/10.1111/jsap.2012.53.issue-2/asset/cover.gif?v=1&amp;s=c148d68b67944e11b7fda4a7e875b3cd02ea9d4d"/><items><rdf:Seq><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01175.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01178.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01180.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01181.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01177.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01165.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01172.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01158.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01155.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01157.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2012.01182.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01163.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01164.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01166.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01167.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01173.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01174.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01147.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01150.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01153.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01171.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01114.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1748-5827.2012.01183.x"/></rdf:Seq></items></channel><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01175.x" xmlns="http://purl.org/rss/1.0/"><title>Thoracoscopic foreign body removal and right middle lung lobectomy to treat pyothorax in a dog</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01175.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Thoracoscopic foreign body removal and right middle lung lobectomy to treat pyothorax in a dog</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Jiménez Peláez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. Jolliffe</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-13T14:01:18.167071-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01175.x</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/j.1748-5827.2011.01175.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01175.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</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>A three-year-old, 30-kg, spayed female German wirehaired pointer was presented for coughing, pyrexia and lethargy. Thoracic radiographs showed mild right-sided pleural effusion, moderate pneumothorax and a pulmonary lesion in the right middle or caudal lung lobe. A diagnosis of pyothorax was established by fine needle aspiration of the pleural effusion. Thoracoscopic exploration was performed using one-lung ventilation. A vegetal foreign body (grass awn) and an abscess were observed in the distal part of the right middle lung lobe. The foreign body was removed and a right middle lung lobectomy was performed, both thoracoscopically. No complications were noted. The dog was discharged 48 hours after surgery, and no recurrence of the clinical signs was observed during the follow-up time period (three years and three months). Thoracoscopy is a minimally invasive alternative to thoracotomy to explore and successfully treat some non-chronic pyothoraces in dogs, including lesions affecting the right middle lung lobe.</p></div>]]></content:encoded><description>A three-year-old, 30-kg, spayed female German wirehaired pointer was presented for coughing, pyrexia and lethargy. Thoracic radiographs showed mild right-sided pleural effusion, moderate pneumothorax and a pulmonary lesion in the right middle or caudal lung lobe. A diagnosis of pyothorax was established by fine needle aspiration of the pleural effusion. Thoracoscopic exploration was performed using one-lung ventilation. A vegetal foreign body (grass awn) and an abscess were observed in the distal part of the right middle lung lobe. The foreign body was removed and a right middle lung lobectomy was performed, both thoracoscopically. No complications were noted. The dog was discharged 48 hours after surgery, and no recurrence of the clinical signs was observed during the follow-up time period (three years and three months). Thoracoscopy is a minimally invasive alternative to thoracotomy to explore and successfully treat some non-chronic pyothoraces in dogs, including lesions affecting the right middle lung lobe.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01178.x" xmlns="http://purl.org/rss/1.0/"><title>Fatal outbreaks in dogs associated with pantropic canine coronavirus in France and Belgium</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01178.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Fatal outbreaks in dogs associated with pantropic canine coronavirus in France and Belgium</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Zicola</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. Jolly</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">E. Mathijs</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">D. Ziant</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. Decaro</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">V. Mari</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">E. Thiry</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-09T13:04:58.134227-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01178.x</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/j.1748-5827.2011.01178.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01178.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</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><b>Infection with pantropic canine coronavirus was detected during outbreaks in France and Belgium. This was concurrent in most cases with canine parvovirus 2c. One outbreak was a deadly acute systemic disease with a single pantropic canine coronavirus infection. This is the first report of a fatality associated with pantropic canine coronavirus alone outside Italy.</b></p></div>]]></content:encoded><description>Infection with pantropic canine coronavirus was detected during outbreaks in France and Belgium. This was concurrent in most cases with canine parvovirus 2c. One outbreak was a deadly acute systemic disease with a single pantropic canine coronavirus infection. This is the first report of a fatality associated with pantropic canine coronavirus alone outside Italy.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01180.x" xmlns="http://purl.org/rss/1.0/"><title>Hand hygiene practices of veterinary support staff in small animal private practice</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01180.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Hand hygiene practices of veterinary support staff in small animal private practice</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. K. Nakamura</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">E. Tompkins</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">E. L. Braasch</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. G. Martinez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">D. Bianco</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-07T03:11:02.468648-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01180.x</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/j.1748-5827.2011.01180.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01180.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</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><b>O<span class="smallCaps">bjective:</span></b><b>To evaluate the hand hygiene (HH) practices among veterinary technicians (VT) and veterinary support staff (VSS) in small animal private practice.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>M<span class="smallCaps">ethods:</span></b><b>This was a prospective questionnaire-based study involving 182 VT and VSS from 18 small animal hospitals in the USA. Questions asked included gender, number of animals handled per work shift, frequency of hand washing, reason for not washing more frequently, most common available hand washing agent, education regarding the importance of HH and frequency of ring wearing.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>R<span class="smallCaps">esults:</span></b><b>Less than half of the respondents [76 of 182 (41·7%)] reported washing their hands regularly between handling patients and 154 of 182 (85·6%) believed they should have washed more frequently. The most commonly employed HH agent was hand soap [154 of 182 (84·6%)] and the most common reason cited for not washing more frequently was being too busy [132 of 182 (72·5%)]. Only 96 of 182 (52·7%) respondents were educated by doctors at their hospital regarding the importance of HH.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>C<span class="smallCaps">linical</span> S<span class="smallCaps">ignificance:</span></b><b>The HH practices among VT and VSS in small animal private practice is poor. Hand soap was the most commonly employed agent among respondents in this study. Education of VT and VSS regarding the importance of HH requires improvement.</b></p></div>]]></content:encoded><description>Objective:To evaluate the hand hygiene (HH) practices among veterinary technicians (VT) and veterinary support staff (VSS) in small animal private practice.Methods:This was a prospective questionnaire-based study involving 182 VT and VSS from 18 small animal hospitals in the USA. Questions asked included gender, number of animals handled per work shift, frequency of hand washing, reason for not washing more frequently, most common available hand washing agent, education regarding the importance of HH and frequency of ring wearing.Results:Less than half of the respondents [76 of 182 (41·7%)] reported washing their hands regularly between handling patients and 154 of 182 (85·6%) believed they should have washed more frequently. The most commonly employed HH agent was hand soap [154 of 182 (84·6%)] and the most common reason cited for not washing more frequently was being too busy [132 of 182 (72·5%)]. Only 96 of 182 (52·7%) respondents were educated by doctors at their hospital regarding the importance of HH.Clinical Significance:The HH practices among VT and VSS in small animal private practice is poor. Hand soap was the most commonly employed agent among respondents in this study. Education of VT and VSS regarding the importance of HH requires improvement.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01181.x" xmlns="http://purl.org/rss/1.0/"><title>Clotrimazole and enilconazole distribution within the frontal sinuses and nasal cavity of nine dogs with sinonasal aspergillosis</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01181.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Clotrimazole and enilconazole distribution within the frontal sinuses and nasal cavity of nine dogs with sinonasal aspergillosis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Sharman</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Z. Lenard</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. Hosgood</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. Mansfield</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-02T07:08:42.002161-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01181.x</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/j.1748-5827.2011.01181.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01181.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</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>O<span class="smallCaps">bjectives</span>: <b>Multiple topical treatments are often required for clinical cure of mycotic rhinosinusitis in dogs. The objective of this study was to describe the distribution and retention of enilconazole and clotrimazole solutions using a temporary trephination protocol.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>M<span class="smallCaps">ethods</span>: <b>Nine client-owned dogs diagnosed with mycotic rhinosinusitis between March 2008 and December 2009 were prospectively enrolled and were sequentially allocated to receive treatment with either clotrimazole (1% in polyethylene glycol) or enilconazole (10% solution), after imaging and rhinoscopic assessment. Both frontal sinuses were trephined, debrided and flushed with saline. Infusion was administered via frontal sinuses with dogs in sternal recumbency and computed tomography (CT) performed 5 minutes after completion. Distribution was scored 1 to 4 at the canine tooth, premolar 4, cribriform plate and frontal sinus on both sides, for a maximum score of 32.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>R<span class="smallCaps">esults</span>: <b>Distribution of antifungal agents to all regions of the nasal cavity and frontal sinuses was achievable, but varied considerably. Retention was poor in 10 of 18 regions assessed.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>C<span class="smallCaps">linical</span> S<span class="smallCaps">ignificance</span>: <b>Distribution of antifungal agents within the frontal sinuses is achievable using temporary trephination; however, distribution is variable and retention is often poor.</b></p></div>]]></content:encoded><description>Objectives: Multiple topical treatments are often required for clinical cure of mycotic rhinosinusitis in dogs. The objective of this study was to describe the distribution and retention of enilconazole and clotrimazole solutions using a temporary trephination protocol.Methods: Nine client-owned dogs diagnosed with mycotic rhinosinusitis between March 2008 and December 2009 were prospectively enrolled and were sequentially allocated to receive treatment with either clotrimazole (1% in polyethylene glycol) or enilconazole (10% solution), after imaging and rhinoscopic assessment. Both frontal sinuses were trephined, debrided and flushed with saline. Infusion was administered via frontal sinuses with dogs in sternal recumbency and computed tomography (CT) performed 5 minutes after completion. Distribution was scored 1 to 4 at the canine tooth, premolar 4, cribriform plate and frontal sinus on both sides, for a maximum score of 32.Results: Distribution of antifungal agents to all regions of the nasal cavity and frontal sinuses was achievable, but varied considerably. Retention was poor in 10 of 18 regions assessed.Clinical Significance: Distribution of antifungal agents within the frontal sinuses is achievable using temporary trephination; however, distribution is variable and retention is often poor.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01177.x" xmlns="http://purl.org/rss/1.0/"><title>Use of a preputial circumferential mucosal flap for hypospadias management in a Boston terrier</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01177.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Use of a preputial circumferential mucosal flap for hypospadias management in a Boston terrier</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Grossman</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">W. Baltzer</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-25T07:39:27.171601-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01177.x</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/j.1748-5827.2011.01177.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01177.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</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><b>An eight-week-old male Boston terrier presented for penile desiccation and urine pooling in the prepuce due to congenital hypospadias. An advancement flap was created from the dorsal mucosa of the incompletely formed prepuce and sutured circumferentially to construct a longer distal preputial mucosa. V- to Y-plasty of the ventral abdominal skin was utilised to create the preputial skin overlying the mucosal flap. Urethrostomy and partial penile amputation were also performed. Following surgery, the clinical signs of penile desiccation and preputial urine pooling resolved and acceptable cosmetic appearance was achieved. This technique may be considered for glandular or penile hypospadias or following resection of the ventral aspect of the distal prepuce when inadequate tissue is present for a simple two-layer closure of the preputial mucosa and skin.</b></p></div>]]></content:encoded><description>An eight-week-old male Boston terrier presented for penile desiccation and urine pooling in the prepuce due to congenital hypospadias. An advancement flap was created from the dorsal mucosa of the incompletely formed prepuce and sutured circumferentially to construct a longer distal preputial mucosa. V- to Y-plasty of the ventral abdominal skin was utilised to create the preputial skin overlying the mucosal flap. Urethrostomy and partial penile amputation were also performed. Following surgery, the clinical signs of penile desiccation and preputial urine pooling resolved and acceptable cosmetic appearance was achieved. This technique may be considered for glandular or penile hypospadias or following resection of the ventral aspect of the distal prepuce when inadequate tissue is present for a simple two-layer closure of the preputial mucosa and skin.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01165.x" xmlns="http://purl.org/rss/1.0/"><title>What’s happened to Staphylococcus intermedius? Taxonomic revision and emergence of multi-drug resistance</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01165.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">What’s happened to Staphylococcus intermedius? Taxonomic revision and emergence of multi-drug resistance</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. Bond</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Loeffler</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-17T11:10:35.173579-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01165.x</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/j.1748-5827.2011.01165.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01165.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</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><em>Staphylococcus intermedius</em> has been the predominant coagulase-positive <em>Staphylococcus</em> isolated from canine skin and mucosae and the most commonly reported staphylococcal pathogen in small animal practice for the last 35 years. Although microbiological tests have historically indicated variability in biochemical characteristics amongst <em>S. intermedius</em> isolates from animals, an acceptable level of diagnostic accuracy for clinical purposes was readily achievable with routine phenotypic testing. However, three recent developments have changed our understanding of the term “<em>S. intermedius</em>” and have challenged veterinary bacteriologists to ensure correct species identification of pathogenic staphylococci from small animals. First, the increasing recognition of meticillin-resistant <em>Staphylococcus aureus</em> in small animal practice and its human health implications demand accurate species identification. Secondly, the application of molecular techniques to analysis of staphylococcal isolates has led to a revised taxonomy and canine isolates of <em>S. intermedius</em> being re-named <em>S. pseudintermedius</em>. Thirdly, the recent, rapid emergence of meticillin- and multi-drug-resistant strains of <em>Staphylococcus pseudintermedius</em> (MRSP) has become a major therapeutic challenge in veterinary practice worldwide, including the UK. This article discusses the background of the recent taxonomic changes within the genus <em>Staphylococcus</em> and reviews the key features of MRSP and its implications for day-to-day laboratory diagnosis and small animal practice.</p></div>]]></content:encoded><description>Staphylococcus intermedius has been the predominant coagulase-positive Staphylococcus isolated from canine skin and mucosae and the most commonly reported staphylococcal pathogen in small animal practice for the last 35 years. Although microbiological tests have historically indicated variability in biochemical characteristics amongst S. intermedius isolates from animals, an acceptable level of diagnostic accuracy for clinical purposes was readily achievable with routine phenotypic testing. However, three recent developments have changed our understanding of the term “S. intermedius” and have challenged veterinary bacteriologists to ensure correct species identification of pathogenic staphylococci from small animals. First, the increasing recognition of meticillin-resistant Staphylococcus aureus in small animal practice and its human health implications demand accurate species identification. Secondly, the application of molecular techniques to analysis of staphylococcal isolates has led to a revised taxonomy and canine isolates of S. intermedius being re-named S. pseudintermedius. Thirdly, the recent, rapid emergence of meticillin- and multi-drug-resistant strains of Staphylococcus pseudintermedius (MRSP) has become a major therapeutic challenge in veterinary practice worldwide, including the UK. This article discusses the background of the recent taxonomic changes within the genus Staphylococcus and reviews the key features of MRSP and its implications for day-to-day laboratory diagnosis and small animal practice.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01172.x" xmlns="http://purl.org/rss/1.0/"><title>Diagnosis and management of oviductal disease in three red-eared slider turtles (Trachemys scripta elegans</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01172.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Diagnosis and management of oviductal disease in three red-eared slider turtles (Trachemys scripta elegans</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. Mans</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. K. Sladky</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-13T08:46:22.587378-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01172.x</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/j.1748-5827.2011.01172.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01172.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</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><b>Three mature, female, red-eared slider turtles <em>(Trachemys scripta elegans)</em> were individually, and separately, diagnosed with different forms of oviductal disease. Case 1 presented with acute cloacal bleeding and was diagnosed with acute oviductal rupture and ectopic eggs in the coelom. Case 2 presented for repeated scratching in the direction of the cloaca and was diagnosed with chronic oviductal impaction and coelomitis. Both cases were treated successfully by endoscopy-assisted complete ovariosalpingectomy via a bilateral prefemoral approach. Case 3 presented with a reduced appetite and signs of nesting behaviour and was diagnosed with obstructive dystocia associated with bacterial salpingitis. Successful treatment consisted of transcloacal egg removal and systemic antibiotics. Complete recovery was achieved in all three turtles, which remained disease-free 23 to 33 months later. Oviductal disease can present with a variety of clinical signs, and an accurate diagnosis can be made based on a thorough history, physical examination and appropriate diagnostic techniques.</b></p></div>]]></content:encoded><description>Three mature, female, red-eared slider turtles (Trachemys scripta elegans) were individually, and separately, diagnosed with different forms of oviductal disease. Case 1 presented with acute cloacal bleeding and was diagnosed with acute oviductal rupture and ectopic eggs in the coelom. Case 2 presented for repeated scratching in the direction of the cloaca and was diagnosed with chronic oviductal impaction and coelomitis. Both cases were treated successfully by endoscopy-assisted complete ovariosalpingectomy via a bilateral prefemoral approach. Case 3 presented with a reduced appetite and signs of nesting behaviour and was diagnosed with obstructive dystocia associated with bacterial salpingitis. Successful treatment consisted of transcloacal egg removal and systemic antibiotics. Complete recovery was achieved in all three turtles, which remained disease-free 23 to 33 months later. Oviductal disease can present with a variety of clinical signs, and an accurate diagnosis can be made based on a thorough history, physical examination and appropriate diagnostic techniques.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01158.x" xmlns="http://purl.org/rss/1.0/"><title>Oestrus ovis infestation of a dog in the UK</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01158.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Oestrus ovis infestation of a dog in the UK</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. McGarry</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">F. Penrose</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. Collins</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-28T14:24:58.666494-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01158.x</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/j.1748-5827.2011.01158.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01158.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</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><b>In March 2011, a dog on a sheep farm in the Cotswolds, UK, expelled a mature live third-stage larva of the sheep nasal botfly, <em>Oestrus ovis</em>, after a violent and traumatic sneezing episode. The dog had been infected with first-stage larvae deposited by an adult fly the previous autumn; larval development had progressed throughout the winter and spring with few apparent clinical signs and possibly masked by ongoing immunotherapy for an unrelated condition. Identification of the parasite at the Liverpool School of Veterinary Science was made from a submitted puparium, the “chrysalis” stage to which the larva had progressed within days of its expulsion from dog’s nose. To the authors’ knowledge this is the first report of nasal botfly infestation of a dog in the UK.</b></p></div>]]></content:encoded><description>In March 2011, a dog on a sheep farm in the Cotswolds, UK, expelled a mature live third-stage larva of the sheep nasal botfly, Oestrus ovis, after a violent and traumatic sneezing episode. The dog had been infected with first-stage larvae deposited by an adult fly the previous autumn; larval development had progressed throughout the winter and spring with few apparent clinical signs and possibly masked by ongoing immunotherapy for an unrelated condition. Identification of the parasite at the Liverpool School of Veterinary Science was made from a submitted puparium, the “chrysalis” stage to which the larva had progressed within days of its expulsion from dog’s nose. To the authors’ knowledge this is the first report of nasal botfly infestation of a dog in the UK.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01155.x" xmlns="http://purl.org/rss/1.0/"><title>Vincristine-induced central neurotoxicity in a collie homozygous for the ABCB1Δ mutation</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01155.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Vincristine-induced central neurotoxicity in a collie homozygous for the ABCB1Δ mutation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">L. Krugman</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. N. Bryan</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. L. Mealey</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Chen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-28T14:23:35.010167-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01155.x</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/j.1748-5827.2011.01155.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01155.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</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><b>A six-year-old, neutered, female collie was presented to an oncology specialty service after developing tetraparesis and self-mutilation that progressively worsened while receiving chemotherapy for lymphoma. Neurologic examination revealed ataxia, paresis and diminished conscious proprioception in all limbs with entire spinal reflexes. Magnetic resonance imaging of the brain and spinal cord was normal. Electromyography of the limbs ruled out a vincristine-induced peripheral neuropathy. Cerebrospinal fluid analysis and cerebrospinal fluid and serum testing for <em>Neospora</em> and <em>Toxoplasma</em> were normal. Results of MDR1 genotyping revealed that the dog was homozygous for the <em>ABCB1-1</em>Δ (<em>MDR1</em>) mutation. This clinical presentation strongly resembled the effects seen from inadvertent intrathecal administration of vincristine in humans. Dogs that are homozygous for the <em>ABCB1-1</em>Δ (<em>MDR1</em>) mutation should not receive standard dosages of chemotherapy drugs known to be eliminated by P-glycoprotein, the gene product of <em>ABCB1</em>. Testing for this mutation is strongly recommended before chemotherapy initiation for at-risk breeds.</b></p></div>]]></content:encoded><description>A six-year-old, neutered, female collie was presented to an oncology specialty service after developing tetraparesis and self-mutilation that progressively worsened while receiving chemotherapy for lymphoma. Neurologic examination revealed ataxia, paresis and diminished conscious proprioception in all limbs with entire spinal reflexes. Magnetic resonance imaging of the brain and spinal cord was normal. Electromyography of the limbs ruled out a vincristine-induced peripheral neuropathy. Cerebrospinal fluid analysis and cerebrospinal fluid and serum testing for Neospora and Toxoplasma were normal. Results of MDR1 genotyping revealed that the dog was homozygous for the ABCB1-1Δ (MDR1) mutation. This clinical presentation strongly resembled the effects seen from inadvertent intrathecal administration of vincristine in humans. Dogs that are homozygous for the ABCB1-1Δ (MDR1) mutation should not receive standard dosages of chemotherapy drugs known to be eliminated by P-glycoprotein, the gene product of ABCB1. Testing for this mutation is strongly recommended before chemotherapy initiation for at-risk breeds.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01157.x" xmlns="http://purl.org/rss/1.0/"><title>Cholesterol granuloma as long-term complication of total ear canal ablation in a dog</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01157.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Cholesterol granuloma as long-term complication of total ear canal ablation in a dog</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">B. Riedinger</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">O. Albaric</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">O. Gauthier</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-28T14:19:55.139123-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01157.x</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/j.1748-5827.2011.01157.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01157.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</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><b>A 13-year-old cocker spaniel presented with pain on opening the mouth. History of a previous left total ear canal ablation with lateral bulla osteotomy, left intermittent facial palsy and left intermittent head tilt suggested progression of a total ear canal ablation with lateral bulla osteotomy complication. Magnetic resonance imaging revealed a large mass arising from the tympanic bulla. Cytology of aspirates revealed a chronic suppurative inflammatory reaction and numerous cholesterol crystals. The mass was removed by surgical excision and an active drainage system was placed for a few days. The head tilt, facial palsy and apparent pain were resolved by the surgery. Physical examination was unremarkable nine months postoperatively. Bacterial cultures of the collected fluid were negative and histological examination confirmed the diagnosis of a cholesterol granuloma.</b></p></div>]]></content:encoded><description>A 13-year-old cocker spaniel presented with pain on opening the mouth. History of a previous left total ear canal ablation with lateral bulla osteotomy, left intermittent facial palsy and left intermittent head tilt suggested progression of a total ear canal ablation with lateral bulla osteotomy complication. Magnetic resonance imaging revealed a large mass arising from the tympanic bulla. Cytology of aspirates revealed a chronic suppurative inflammatory reaction and numerous cholesterol crystals. The mass was removed by surgical excision and an active drainage system was placed for a few days. The head tilt, facial palsy and apparent pain were resolved by the surgery. Physical examination was unremarkable nine months postoperatively. Bacterial cultures of the collected fluid were negative and histological examination confirmed the diagnosis of a cholesterol granuloma.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2012.01182.x" xmlns="http://purl.org/rss/1.0/"><title>Surgical therapy for canine congenital valvular pulmonic stenosis: when and how?</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2012.01182.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Surgical therapy for canine congenital valvular pulmonic stenosis: when and how?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Daniel J Brockman</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2012.01182.x</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/j.1748-5827.2012.01182.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2012.01182.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">87</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">88</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01163.x" xmlns="http://purl.org/rss/1.0/"><title>Surgical treatment of severe pulmonic stenosis under cardiopulmonary bypass in small dogs</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01163.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Surgical treatment of severe pulmonic stenosis under cardiopulmonary bypass in small dogs</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Fujiwara</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. Harada</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">T. Mizuno</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Nishida</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">T. Mizukoshi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Mizuno</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Uechi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01163.x</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/j.1748-5827.2011.01163.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01163.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">89</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">94</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><b>O<span class="smallCaps">bjectives</span>: The aim of this study was to report the long-term outcome of the surgical palliation of pulmonic stenosis in dogs.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>M<span class="smallCaps">ethods</span>: The subjects comprised three female and six male dogs, mean (±sd) age: 23 (±25) months, mean (±sd) weight: 3·4 (±2·1) kg, diagnosed with severe pulmonic stenosis and right ventricular hypertrophy, with an average preoperative pressure gradient of 153 (±43) mmHg on echocardiography.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>R<span class="smallCaps">esults</span>: The pressure overload with severe pulmonic stenosis was reduced by valvotomy, i.e., open pulmonary valve commissurotomy, with/without biomembrane patch grafting, under cardiopulmonary bypass. The postoperative pressure gradient at 1 to 7 days was significantly decreased to 65 (±39) mmHg (P&lt;0·05). The reduced pressure gradient was maintained at 58 (±38) mmHg at final follow-up.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>C<span class="smallCaps">linical</span> S<span class="smallCaps">ignificance</span>: Open valvotomy, pulmonary valve commissurotomy and biomembrane patch grafting were effective in reducing obstruction in severe pulmonic stenosis in dogs.</b></p></div>]]></content:encoded><description>Objectives: The aim of this study was to report the long-term outcome of the surgical palliation of pulmonic stenosis in dogs.Methods: The subjects comprised three female and six male dogs, mean (±sd) age: 23 (±25) months, mean (±sd) weight: 3·4 (±2·1) kg, diagnosed with severe pulmonic stenosis and right ventricular hypertrophy, with an average preoperative pressure gradient of 153 (±43) mmHg on echocardiography.Results: The pressure overload with severe pulmonic stenosis was reduced by valvotomy, i.e., open pulmonary valve commissurotomy, with/without biomembrane patch grafting, under cardiopulmonary bypass. The postoperative pressure gradient at 1 to 7 days was significantly decreased to 65 (±39) mmHg (P&lt;0·05). The reduced pressure gradient was maintained at 58 (±38) mmHg at final follow-up.Clinical Significance: Open valvotomy, pulmonary valve commissurotomy and biomembrane patch grafting were effective in reducing obstruction in severe pulmonic stenosis in dogs.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01164.x" xmlns="http://purl.org/rss/1.0/"><title>Distribution and persistence of topical clotrimazole after sinus infusion in normal canine cadavers</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01164.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Distribution and persistence of topical clotrimazole after sinus infusion in normal canine cadavers</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. M. Hayes</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. L. Demetriou</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01164.x</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/j.1748-5827.2011.01164.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01164.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">95</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">100</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><b>O<span class="smallCaps">bjectives</span>: To determine the in vitro persistence of clotrimazole 1% cream in the canine frontal sinus and to evaluate the distribution of clotrimazole solution over the sino-nasal mucosa using a previously described surgical treatment protocol for canine nasal aspergillosis.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>M<span class="smallCaps">ethods</span>: Two canine skulls were used to monitor the persistence of clotrimazole cream in the lateral frontal sinus at 37°C. The distribution of irrigation solution around the frontal sinus compartments and nasal cavity was determined using six canine cadaver heads by trephining either the lateral or both the lateral and rostral compartments of the frontal sinus. Stain was added to the sinus irrigation solution before visually inspecting the sagittally sectioned heads.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>R<span class="smallCaps">esults</span>: Clotrimazole cream persisted in the frontal sinus for at least 96 hours. The nasal cavity mucosa was completely stained in 8 of 12 sides and almost completely stained in the remaining 4 of 12 sides. Flushing irrigation solution through the lateral compartment of the frontal sinus resulted in inadequate staining of the rostral compartment but medicating both the lateral and rostral compartments resulted in complete coating of all frontal sinus mucosa in eight of eight sides.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>C<span class="smallCaps">linical</span> S<span class="smallCaps">ignificance</span>: Clotrimazole cream has the potential to be retained in the frontal sinus for several days and is distributed effectively in normal canine cadavers. Medicating both the rostral and lateral compartments of the frontal sinus may be indicated in some clinical cases.</b></p></div>]]></content:encoded><description>Objectives: To determine the in vitro persistence of clotrimazole 1% cream in the canine frontal sinus and to evaluate the distribution of clotrimazole solution over the sino-nasal mucosa using a previously described surgical treatment protocol for canine nasal aspergillosis.Methods: Two canine skulls were used to monitor the persistence of clotrimazole cream in the lateral frontal sinus at 37°C. The distribution of irrigation solution around the frontal sinus compartments and nasal cavity was determined using six canine cadaver heads by trephining either the lateral or both the lateral and rostral compartments of the frontal sinus. Stain was added to the sinus irrigation solution before visually inspecting the sagittally sectioned heads.Results: Clotrimazole cream persisted in the frontal sinus for at least 96 hours. The nasal cavity mucosa was completely stained in 8 of 12 sides and almost completely stained in the remaining 4 of 12 sides. Flushing irrigation solution through the lateral compartment of the frontal sinus resulted in inadequate staining of the rostral compartment but medicating both the lateral and rostral compartments resulted in complete coating of all frontal sinus mucosa in eight of eight sides.Clinical Significance: Clotrimazole cream has the potential to be retained in the frontal sinus for several days and is distributed effectively in normal canine cadavers. Medicating both the rostral and lateral compartments of the frontal sinus may be indicated in some clinical cases.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01166.x" xmlns="http://purl.org/rss/1.0/"><title>Clinical and magnetic resonance imaging features of canine compressive cervical myelopathy with suspected hydrated nucleus pulposus extrusion</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01166.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Clinical and magnetic resonance imaging features of canine compressive cervical myelopathy with suspected hydrated nucleus pulposus extrusion</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">E. Beltran</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. Dennis</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">V. Doyle</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. 
            De Stefani</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Holloway</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">L. 
            De Risio</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01166.x</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/j.1748-5827.2011.01166.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01166.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">101</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">107</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><b>O<span class="smallCaps">bjective</span>: To describe clinical and magnetic resonance imaging features in dogs with compressive cervical myelopathy due to acute suspected hydrated nucleus pulposus extrusion.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>D<span class="smallCaps">esign</span>: Retrospective case series.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>A<span class="smallCaps">nimals</span>: Ten dogs with compressive cervical myelopathy caused by acute suspected hydrated nucleus pulposus extrusion.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>M<span class="smallCaps">aterials and</span> M<span class="smallCaps">ethods</span>: Medical records and magnetic resonance images of dogs evaluated from 2005 through 2010 were reviewed. The inclusion criteria were clinical signs compatible with cervical myelopathy, magnetic resonance imaging of the spine performed within 48 hours after onset, magnetic resonance imaging findings consistent with compressive suspected hydrated nucleus pulposus extrusion, complete medical records and follow-up information.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>R<span class="smallCaps">esults</span>: Six dogs were presented with acute onset tetraplegia and four dogs with acute onset of nonambulatory tetraparesis. Compromised respiratory function was present in three dogs. Compressive suspected hydrated nucleus pulposus extrusion was found on magnetic resonance imaging at the C4-C5 (n=6), C3-C4 (n=3) and C5-C6 (n=1) intervertebral disc spaces. Seven dogs underwent surgical treatment and three dogs were treated conservatively. All dogs except one regained ambulatory status within two weeks after the onset, and had a favourable outcome.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>C<span class="smallCaps">linical</span> S<span class="smallCaps">ignificance</span>: Compressive myelopathy caused by acute suspected hydrated nucleus pulposus extrusion has not been reported previously and, even though neurological deficits can be severe on presentation, outcome is favourable.</b></p></div>]]></content:encoded><description>Objective: To describe clinical and magnetic resonance imaging features in dogs with compressive cervical myelopathy due to acute suspected hydrated nucleus pulposus extrusion.Design: Retrospective case series.Animals: Ten dogs with compressive cervical myelopathy caused by acute suspected hydrated nucleus pulposus extrusion.Materials and Methods: Medical records and magnetic resonance images of dogs evaluated from 2005 through 2010 were reviewed. The inclusion criteria were clinical signs compatible with cervical myelopathy, magnetic resonance imaging of the spine performed within 48 hours after onset, magnetic resonance imaging findings consistent with compressive suspected hydrated nucleus pulposus extrusion, complete medical records and follow-up information.Results: Six dogs were presented with acute onset tetraplegia and four dogs with acute onset of nonambulatory tetraparesis. Compromised respiratory function was present in three dogs. Compressive suspected hydrated nucleus pulposus extrusion was found on magnetic resonance imaging at the C4-C5 (n=6), C3-C4 (n=3) and C5-C6 (n=1) intervertebral disc spaces. Seven dogs underwent surgical treatment and three dogs were treated conservatively. All dogs except one regained ambulatory status within two weeks after the onset, and had a favourable outcome.Clinical Significance: Compressive myelopathy caused by acute suspected hydrated nucleus pulposus extrusion has not been reported previously and, even though neurological deficits can be severe on presentation, outcome is favourable.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01167.x" xmlns="http://purl.org/rss/1.0/"><title>Complications associated with temporary tracheostomy tubes in 42 dogs (1998 to 2007)</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01167.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Complications associated with temporary tracheostomy tubes in 42 dogs (1998 to 2007)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">I. Nicholson</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. Baines</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01167.x</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/j.1748-5827.2011.01167.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01167.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">108</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">114</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><b>O<span class="smallCaps">bjective</span>: To identify the type and frequency of tracheostomy tube complications, and to determine factors associated with these complications, and with poor outcome.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>M<span class="smallCaps">ethods</span>: A database search for dogs undergoing temporary tube tracheostomy was performed. The medical records were scrutinised. The signalment, respiratory disease history, diagnosis, surgery, type and frequency of tube care procedures, type of complications and outcome were recorded.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>R<span class="smallCaps">esults</span>: Forty-two records were found. Complications occurred in 36 of 42 (86%) cases. Bulldogs were more likely to dislodge the tube than other breeds (P=0·0376), and cases with three or more complication types underwent more routine care procedures than those with fewer complications (P=0·0370). Thirty-four of 42 (81%) dogs had a successfully managed tracheostomy tube and survived until tube removal, or elective euthanasia without significant tube complications. Bulldogs were also significantly (P=0·0376) more likely to have an unsuccessful tube outcome, as were dogs experiencing severe bradycardia during treatment (P=0·0176). Dogs with unsuccessful tube outcome were significantly (P=0·0331) younger than dogs with successful tube outcome.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>C<span class="smallCaps">linical</span> S<span class="smallCaps">ignificance</span>: Tracheostomy tubes in dogs have a high complication rate but a good outcome in most dogs. Careful management may improve the outcome of dogs with tracheostomy tubes, especially bulldogs and dogs exhibiting bradycardia during treatment.</b></p></div>]]></content:encoded><description>Objective: To identify the type and frequency of tracheostomy tube complications, and to determine factors associated with these complications, and with poor outcome.Methods: A database search for dogs undergoing temporary tube tracheostomy was performed. The medical records were scrutinised. The signalment, respiratory disease history, diagnosis, surgery, type and frequency of tube care procedures, type of complications and outcome were recorded.Results: Forty-two records were found. Complications occurred in 36 of 42 (86%) cases. Bulldogs were more likely to dislodge the tube than other breeds (P=0·0376), and cases with three or more complication types underwent more routine care procedures than those with fewer complications (P=0·0370). Thirty-four of 42 (81%) dogs had a successfully managed tracheostomy tube and survived until tube removal, or elective euthanasia without significant tube complications. Bulldogs were also significantly (P=0·0376) more likely to have an unsuccessful tube outcome, as were dogs experiencing severe bradycardia during treatment (P=0·0176). Dogs with unsuccessful tube outcome were significantly (P=0·0331) younger than dogs with successful tube outcome.Clinical Significance: Tracheostomy tubes in dogs have a high complication rate but a good outcome in most dogs. Careful management may improve the outcome of dogs with tracheostomy tubes, especially bulldogs and dogs exhibiting bradycardia during treatment.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01173.x" xmlns="http://purl.org/rss/1.0/"><title>Urine specific gravity values in clinically healthy young pet ferrets (Mustela furo)</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01173.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Urine specific gravity values in clinically healthy young pet ferrets (Mustela furo)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">D. Eshar</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. R. Wyre</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">D. C. Brown</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01173.x</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/j.1748-5827.2011.01173.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01173.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">115</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">119</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><b>O<span class="smallCaps">bjectives</span>: To determine urine specific gravity values in clinically healthy pet ferrets and explore possible associations with sex, sampling techniques, hydration status and urine analytes.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>M<span class="smallCaps">ethods</span>: Sixty-nine entire ferrets of both sexes, under one year of age, were included in this study. Physical examination, complete blood count, blood biochemistry, urine microscopy, urine dipstick and urine specific gravity were performed on all ferrets. Urine specific gravity was determined using a handheld urine refractometer. Statistical analysis was performed to determine urine specific gravity value intervals and to test for associations with sex, sample collection method, packed cell volume, plasma total protein concentrations and urine analytes.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>R<span class="smallCaps">esults</span>: Urine specific gravity differed by sex in ferrets as females exhibited a lower urine specific gravity (P&lt;0·001). There was no significant correlation between urine specific gravity, sampling method, packed cell volume/total protein and urine dipstick analytes. Mean urine specific gravity reported in this study was 1·051 for entire males (sd ±9; range 1·034 to 1·070) and 1·042 for entire females (sd ±8; range 1·026 to 1·060).</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>C<span class="smallCaps">linical</span> S<span class="smallCaps">ignificance</span>: Results of this study may allow clinicians to have a more accurate evaluation of the ability of those animals to concentrate urine by comparing their urine specific gravity results to those obtained from this cohort of clinically healthy animals.</b></p></div>]]></content:encoded><description>Objectives: To determine urine specific gravity values in clinically healthy pet ferrets and explore possible associations with sex, sampling techniques, hydration status and urine analytes.Methods: Sixty-nine entire ferrets of both sexes, under one year of age, were included in this study. Physical examination, complete blood count, blood biochemistry, urine microscopy, urine dipstick and urine specific gravity were performed on all ferrets. Urine specific gravity was determined using a handheld urine refractometer. Statistical analysis was performed to determine urine specific gravity value intervals and to test for associations with sex, sample collection method, packed cell volume, plasma total protein concentrations and urine analytes.Results: Urine specific gravity differed by sex in ferrets as females exhibited a lower urine specific gravity (P&lt;0·001). There was no significant correlation between urine specific gravity, sampling method, packed cell volume/total protein and urine dipstick analytes. Mean urine specific gravity reported in this study was 1·051 for entire males (sd ±9; range 1·034 to 1·070) and 1·042 for entire females (sd ±8; range 1·026 to 1·060).Clinical Significance: Results of this study may allow clinicians to have a more accurate evaluation of the ability of those animals to concentrate urine by comparing their urine specific gravity results to those obtained from this cohort of clinically healthy animals.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01174.x" xmlns="http://purl.org/rss/1.0/"><title>Magnetic resonance imaging enhancement of intervertebral disc disease in 30 dogs following chemical fat saturation</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01174.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Magnetic resonance imaging enhancement of intervertebral disc disease in 30 dogs following chemical fat saturation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. C. Freeman</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. R. Platt</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Kent</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">E. Howerth</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. P. Holmes</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01174.x</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/j.1748-5827.2011.01174.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01174.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">120</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">125</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><b>O<span class="smallCaps">bjective</span>: To describe the patterns of enhancement of extradural intervertebral disc on chemically fat saturated gadolinium-enhanced magnetic resonance images and to investigate the clinical and pathological associations with enhancement.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>M<span class="smallCaps">ethods</span>: Medical records and magnetic resonance images were reviewed from 30 dogs with histopathologically confirmed disc disease and enhancement on a T1-weighted postcontrast fat saturated sequence.</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>R<span class="smallCaps">esults</span>: Median duration of neurological signs was 4 days and the most common grade of severity was II, seen in 46·6% of dogs. Homogeneous, heterogeneous and peripheral patterns of disc enhancement were described, with peripheral enhancement most commonly identified (57% of dogs). There were no clinical or pathological differences between the dogs with each of the patterns. The mean signal intensity of a region of interest within the extruded disc material and contrast-to-noise ratio of the disc material were significantly higher on postcontrast T1-weighted fat saturated images (P=&lt;0·0001 each).</b></p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>C<span class="smallCaps">linical</span> S<span class="smallCaps">ignificance</span>: The use of fat saturated gadolinium-enhanced magnetic resonance imaging can detect enhancement of extradural disc material. Patterns of enhancement are not associated with the clinical presentation or pathological features.</b></p></div>]]></content:encoded><description>Objective: To describe the patterns of enhancement of extradural intervertebral disc on chemically fat saturated gadolinium-enhanced magnetic resonance images and to investigate the clinical and pathological associations with enhancement.Methods: Medical records and magnetic resonance images were reviewed from 30 dogs with histopathologically confirmed disc disease and enhancement on a T1-weighted postcontrast fat saturated sequence.Results: Median duration of neurological signs was 4 days and the most common grade of severity was II, seen in 46·6% of dogs. Homogeneous, heterogeneous and peripheral patterns of disc enhancement were described, with peripheral enhancement most commonly identified (57% of dogs). There were no clinical or pathological differences between the dogs with each of the patterns. The mean signal intensity of a region of interest within the extruded disc material and contrast-to-noise ratio of the disc material were significantly higher on postcontrast T1-weighted fat saturated images (P=&lt;0·0001 each).Clinical Significance: The use of fat saturated gadolinium-enhanced magnetic resonance imaging can detect enhancement of extradural disc material. Patterns of enhancement are not associated with the clinical presentation or pathological features.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01147.x" xmlns="http://purl.org/rss/1.0/"><title>Symptomatic treatment of ascites with a peritoneo-vesical automated fluid shunt system in a dog</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01147.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Symptomatic treatment of ascites with a peritoneo-vesical automated fluid shunt system in a dog</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. Venzin</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">P. Kook</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. Jenni</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. Wilhelm</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">T. Degen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Braun</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Rütten</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">T. M. Glaus</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01147.x</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/j.1748-5827.2011.01147.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01147.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">126</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">131</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><b>A six-year-old Rottweiler with chronic ascites and moderate panhypoproteinaemia that had been treated with large volume paracentesis over several months duration was diagnosed with a large bi-atrial mass and hepatic fibrosis. For palliative treatment, a peritoneo-vesical automated fluid shunt system with an integrated chargeable battery and an integrated computer to control pump function and to transmit data transcutaneously was implanted by coeliotomy. The pump was left in place for 10 weeks, eliminating the need for further paracentesis during this time. At the end of this period, no ascites was discernible and serum protein concentrations had returned to their respective reference intervals. As a complication, decubitus with skin perforation had developed above the pump. Besides palliative treatment of chronic refractory ascites, this pump may have application in other conditions characterised by chronic cavity effusion or in peritoneal dialysis.</b></p></div>]]></content:encoded><description>A six-year-old Rottweiler with chronic ascites and moderate panhypoproteinaemia that had been treated with large volume paracentesis over several months duration was diagnosed with a large bi-atrial mass and hepatic fibrosis. For palliative treatment, a peritoneo-vesical automated fluid shunt system with an integrated chargeable battery and an integrated computer to control pump function and to transmit data transcutaneously was implanted by coeliotomy. The pump was left in place for 10 weeks, eliminating the need for further paracentesis during this time. At the end of this period, no ascites was discernible and serum protein concentrations had returned to their respective reference intervals. As a complication, decubitus with skin perforation had developed above the pump. Besides palliative treatment of chronic refractory ascites, this pump may have application in other conditions characterised by chronic cavity effusion or in peritoneal dialysis.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01150.x" xmlns="http://purl.org/rss/1.0/"><title>Severe systemic hypertension in a cat with pituitary-dependent hyperadrenocorticism</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01150.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Severe systemic hypertension in a cat with pituitary-dependent hyperadrenocorticism</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. L. Brown</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. A. Beatty</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. A. Lindsay</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">V. R. Barrs</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01150.x</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/j.1748-5827.2011.01150.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01150.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">132</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">135</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><b>A seven-year-old Burmese cat was presented with sudden onset blindness. On physical examination, the cat had bilateral retinal detachment and severe systemic hypertension. Further clinical investigations revealed pituitary-dependent hyperadrenocorticism. Antihypertensive therapy was discontinued when the hypertension resolved after bilateral adrenalectomy. Systolic blood pressure remained normal until 19 months post-operatively when systemic hypertension recurred and was attributed to chronic kidney disease. The cat was euthanased 47 months after initial presentation. A pituitary adenoma was identified at post-mortem examination. This case illustrates that systemic hypertension can occur secondary to hyperadrenocorticism in the cat.</b></p></div>]]></content:encoded><description>A seven-year-old Burmese cat was presented with sudden onset blindness. On physical examination, the cat had bilateral retinal detachment and severe systemic hypertension. Further clinical investigations revealed pituitary-dependent hyperadrenocorticism. Antihypertensive therapy was discontinued when the hypertension resolved after bilateral adrenalectomy. Systolic blood pressure remained normal until 19 months post-operatively when systemic hypertension recurred and was attributed to chronic kidney disease. The cat was euthanased 47 months after initial presentation. A pituitary adenoma was identified at post-mortem examination. This case illustrates that systemic hypertension can occur secondary to hyperadrenocorticism in the cat.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01153.x" xmlns="http://purl.org/rss/1.0/"><title>Duodenal Brunner's gland adenoma causing chronic small intestinal obstruction in a dog</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01153.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Duodenal Brunner's gland adenoma causing chronic small intestinal obstruction in a dog</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">E. J. Bowen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">P. Mundy</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. S. Tivers</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. M. Syme</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">P. Mantis</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">B. Smyth</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. J. Baines</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01153.x</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/j.1748-5827.2011.01153.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01153.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">136</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">139</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><b>An eight-year-old, neutered, female English springer spaniel was presented with a 14-month history of vomiting, marked weight loss and lethargy, all of which were non-responsive to medical therapy. Abdominal radiographs and ultrasonography showed an intraluminal soft tissue mass extending from the pyloric antrum to the proximal duodenum. Two spherical masses both approximately 8 cm in diameter were removed via a duodenotomy. Histopathological examination showed the first mass to be a trichobezoar and the aboral mass to be a Brunner's gland adenoma. Surgery resulted in a complete resolution of the clinical signs.</b></p></div>]]></content:encoded><description>An eight-year-old, neutered, female English springer spaniel was presented with a 14-month history of vomiting, marked weight loss and lethargy, all of which were non-responsive to medical therapy. Abdominal radiographs and ultrasonography showed an intraluminal soft tissue mass extending from the pyloric antrum to the proximal duodenum. Two spherical masses both approximately 8 cm in diameter were removed via a duodenotomy. Histopathological examination showed the first mass to be a trichobezoar and the aboral mass to be a Brunner's gland adenoma. Surgery resulted in a complete resolution of the clinical signs.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01171.x" xmlns="http://purl.org/rss/1.0/"><title>Clinical research in practice: animal test certificates</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01171.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Clinical research in practice: animal test certificates</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Helen Jukes</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Katharine Healey</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01171.x</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/j.1748-5827.2011.01171.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01171.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">140</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">140</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01114.x" xmlns="http://purl.org/rss/1.0/"><title>Feline Emergency and Critical Care Medicine</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01114.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Feline Emergency and Critical Care Medicine</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gabrielle Musk</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2011.01114.x</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/j.1748-5827.2011.01114.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2011.01114.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">141</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">141</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1748-5827.2012.01183.x" xmlns="http://purl.org/rss/1.0/"><title>BSAVA Manual of Canine and Feline Ultrasonography</title><link>http://dx.doi.org/10.1111%2Fj.1748-5827.2012.01183.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">BSAVA Manual of Canine and Feline Ultrasonography</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nicolette Hayward</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-5827.2012.01183.x</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/j.1748-5827.2012.01183.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1748-5827.2012.01183.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">143</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">143</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item></rdf:RDF>
