Please see the Glossary of terms in Appendix 1 for additional information and definitions.
Description of the condition
Skin and soft tissue infections (SSTIs) are common infections of the epidermis, dermis, or subcutaneous tissue and characterised by induration (hardening), erythema (redness), warmth and pain or tenderness and range from mild, self-limiting furunculosis (boils) to life-threatening necrotising fasciitis (Stevens 2005). SSTIs include:
- Abscesses, cellulitis (infection just under the skin), and erysipelas (skin infection).
- Necrotising skin and soft-tissue infections.
- Infections following animal and human bites.
- Soft-tissue infections following animal contact.
- Surgical site infections.
- Infections in people whose immune systems are compromised.
- Infections resulting from treatment (i.e. iatrogenic) (e.g. postoperative wounds).
The Food and Drugs Administration (FDA) classifies SSTIs as either "uncomplicated" or "complicated". Uncomplicated SSTIs are superficial infections and simple surgical incisions amenable to treatment with antibiotics, e.g. simple abscesses, carbuncles, impetigo lesions, furuncles (boils), and cellulitis. Complicated SSTIs are infections involving the deeper tissues, such as subcutaneous tissue, fascia, and skeletal muscle, or SSTIs in patients with co-morbidities such as diabetes mellitus, HIV, and other immunocompromised states (FDA 1998). SSTIs are caused by a wide variety of organisms, most of which are Gram-positive (i.e. are stained by a particular biological dye). The SENTRY Antimicrobial Surveillance Program has been monitoring SSTIs in more than 70 medical centres in North America, Europe, Latin America, and the Asia-Pacific region since 1997. Their report, which presents data over a seven year period (1998 to 2004), ranks SSTIs by frequency of pathogen as follows: Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, Enterococcus species, Klebsiella species, Enterobacter species, β-haemolytic streptococci, coagulase-negative staphylococci, Proteus mirabilis, and Acinetobacter species (Fritsche 2007). The complications of SSTIs, particularly those caused by Staphylococcus aureus, may cause bacteraemia (bacteria in the blood) and induce focal points of infection, such as bacterial endocarditis (the lining of the heart), osteomyelitis (bones), brain abscesses, brain meningitis, and/or lung abscesses (Eisenstein 2008), at a distance from the original infection.
The morbidity and treatment costs associated with SSTIs are high, and treatment has become more complex recently due to the increasing prevalence of multidrug-resistant pathogens (Moet 2006). During the past decade the prevalence of antibiotic resistance among Gram-positive cocci (bacteria) - particularly Staphylococcus aureus - has increased sharply. A considerable variation in the methicillin-resistant Staphylococcus aureus (MRSA) rate was noted between countries and continents. According to the SENTRY report, the MRSA infection rate of all infections was 35.9 per cent in North America, compared with 29.4 per cent in Latin America and 22.8 per cent in Europe. The MRSA rate of all infections varied considerably among the European countries too, ranging from 0.8 per cent in Sweden to 50 per cent in Portugal (Fritsche 2007). Variability in MRSA infection rate was also apparent in Latin America, where Mexico had 50 per cent of all infections, Chile 38 per cent, Brazil 29 per cent, Argentina 28 per cent, and Columbia and Venezuela combined had 3 per cent (Moet 2006). Antibiotic resistance increases the length of stay in hospital, costs of treatment and the mortality rate. A review of the epidemiology of severe Staphylococcus aureus infections in Europe reports that the overall seven-day case fatality rate was 19 per cent (Lamagni 2008). A US study reported that patients with MRSA-infected surgical sites had a three times greater 90-day mortality rate and a greater duration of hospitalisation after infection (median additional days 5; P value less than 0.001) than patients infected by methicillin-sensitiveStaphylococcus aureus (MSSA). Median hospital charges were USD 92,363 for patients with MRSA surgical site infections compared with USD 52,791 for patients with MSSA infections (Engemann 2003).
Description of the intervention
The treatment of uncomplicated SSTIs and complicated SSTIs differs, with different clinical outcomes. Uncomplicated SSTIs are usually treated locally with, or without, antibiotics, whereas most complicated SSTIs require hospitalisation, treatment with intravenous antibiotics, and possibly surgical intervention (Eron 2003). Choice of the initial antibiotic is crucial for patients with complicated SSTIs. It has been demonstrated that correct use of antibiotics is associated with lower morbidity and mortality in patients who have an infection (Bouza 2004).
The antibiotics commonly used for the treatment of SSTIs caused by Gram-positive cocci are beta-lactams (including semisynthetic penicillins and cephalosporins), clindamycin, vancomycin, and linezolid (Fung 2003). Beta-lactam antibiotics remain the mainstay of treatment for suspected streptococcal and MMSA infections. In proven penicillin-sensitive infection, use of benzyl penicillin remains appropriate. Clindamycin can be administered in combination with beta-lactam antibiotics for rapidly-progressing infections, such as severe streptococcal infections, where beta-lactam antibiotics alone are less effective. During the past decade the prevalence of antibiotic resistance among Gram-positive cocci (e.g. MRSA) has increased sharply. Vancomycin has been the mainstay of therapy in MRSA infections and for patients who are intolerant of or allergic to the beta-lactams. Linezolid is a novel oxazolidinone agent for use against staphylococci and enterococci, with a spectrum of activity against Gram-positive bacteria similar to that of vancomycin. So linezolid and vancomycin are often compared.
How the intervention might work
Mechanism of action
Vancomycin is a traditional antibiotic for the treatment of Gram-positive cocci, especially MRSA, which acts by inhibiting proper cell wall synthesis in Gram-positive bacteria. Due to the different mechanism by which Gram-negative bacteria produce their cell walls, and the various factors related to entering the outer membrane of Gram-negative organisms, vancomycin is not active against Gram-negative bacteria (except some non-gonococcal species of Neisseria).
Linezolid, the first member of the oxazolidinone class of antibiotics to be approved by the FDA, is indicated for the treatment of SSTIs caused by methicillin-sensitive or methicillin-resistant S aureus, or vancomycin-resistant enterococci and other susceptible micro-organisms (Fung 2001). Linezolid has a unique mechanism of action. It stops the growth and reproduction of bacteria by disrupting translation of messenger RNA into proteins in the ribosome. Linezolid selectively binds to the 50S ribosomal unit and inhibits initiation of complex protein synthesis (Wilson 2008). This unique mechanism has not been seen in any other antibiotic agents, thus, cross-resistance of linezolid has not been observed. One of the advantages of linezolid is its high bioavailability when given by mouth (close to 100 per cent). This means that people receiving intravenous linezolid may be switched to oral linezolid as soon as their condition allows it, whereas vancomycin can only be given intravenously (Moellering 1999).
During recent years, the decreasing susceptibility of some bacteria to traditional antibiotics has been a significant problem in treating SSTIs. The increasing incidence of infections caused by resistant Gram-positive cocci has led to a sharp increase in the use of vancomycin (Pallares 1993). As a result, the emergence of vancomycin-resistant strains of enterococci and staphylococci has been widely observed in the last few years. Between the years 1998 to 2004 vancomycin-resistant enterococci increased in Europe to 4.1 per cent, and in North America to 6.2 per cent (Fritsche 2007)
The resistance of Gram-positive bacteria to linezolid has not been noted to the same extent. Linezolid-resistant Staphylococcus aureus was first isolated in 2001 (Tsiodras 2001). The seventh year of the Zyvox Annual Appraisal of Potency and Spectrum Program (2008) monitored the in vitro activities of linezolid and comparator agents tested against Gram-positive pathogens in Latin America, Europe, Canada, and the Asia-Pacific region. Overall resistance to linezolid in 23 countries was only 0.13 per cent across all monitored Gram-positive pathogens. Oxazolidinone-resistant strains continued to be identified in several nations (Brazil, China, France, Germany, Italy, and Sweden) and among three prevalent pathogen groups (S aureus, coagulase-negative staphylococci, and enterococci) (Jones 2009).
The common adverse reactions indicated for vancomycin are nephrotoxicity (damage to kidneys) and ototoxicity (damage to ears) (Finch 2005). These adverse reactions were both side-effects of early, impure versions of vancomycin (Levine 2006). Later trials, that used purer forms of vancomycin, found that, while renal toxicity (kidney damage) is an infrequent adverse effect, it is accentuated by the presence of aminoglycosides (Finch 2005). Erythroderma (red man syndrome) may also occur. This syndrome is an allergic reaction characterised by the flushing of the upper body, with itching due to histamine release (Sivagnanam 2003).
When used for short periods, linezolid is a relatively safe drug. Long-term use of linezolid has been associated with bone marrow suppression, which is characterised particularly by thrombocytopenia (low blood platelet count). Thrombocytopenia appears to be the only adverse effect that occurs significantly more frequently with linezolid than with glycopeptides or beta-lactams (Falagas 2008).
Why it is important to do this review
Several studies have compared linezolid with vancomycin; the outcomes were inconsistent. Other reviews have reported that linezolid is more effective than vancomycin in the treatment of SSTIs caused by Gram-positive bacteria or MRSA (Beibei 2010; Bounthavong 2010; Falagas 2008). The outcome from another systematic review (Dodds 2009), however, showed that there is no statistically significant difference between linezolid with vancomycin. It disagreed with the conclusions of the other three reviews. Until now, there has been no Cochrane systematic review to summarise the evidence for the beneficial and adverse effects of linezolid compared with vancomycin in people with SSTIs.
To compare the effects of linezolid and vancomycin for treating skin and soft tissue infections.
Criteria for considering studies for this review
Types of studies
We included all randomised controlled trials (RCTs) that compared linezolid with vancomycin in the treatment of skin and soft tissue infections.
Types of participants
We included people of any age or gender presenting with skin and soft tissue infections (e.g. cellulitis, erysipelas, furuncles, simple abscesses, wound infections, and deeper infections such as necrotising fasciitis, myositis (inflammation of muscles), and gas gangrene).
Types of interventions
Any dose of linezolid or vancomycin, by any route.
We intended to present comparisons as follows:
1. Linezolid compared with vancomycin alone.
2. Linezolid plus co-interventions compared with vancomycin plus co-interventions.
Co-interventions might include other antibiotics for use against Gram-negative bacteria, or other routine medications and surgical interventions, as long as participants in the different trial arms had equal access to such co-interventions.
Types of outcome measures
1. Clinical cure (resolution of symptoms and signs) and microbiological cure (eradication of bacteria on wound culture).
Proportion of patients or infections healed. We defined healing as either the resolution of all clinical signs and symptoms of infection as assessed by laboratory test or defined by trialists, or microbiological cure (i.e. eradication of MRSA on wound culture).
2. SSTI-related and treatment-related mortality.
- Adverse events.
- Duration of hospital stay.
- Duration of treatment.
Search methods for identification of studies
In May 2013 we searched the following electronic databases to find reports of relevant RCTs:
- The Cochrane Wounds Group Specialised Register (searched 9 May 2013);
- The Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library 2013, Issue 4);
- Ovid MEDLINE (1950 to April Week 4 2013);
- Ovid MEDLINE (In-Process & Other Non-Indexed Citations, May 08 2013);
- Ovid EMBASE (1980 to 2013 Week 18);
- EBSCO CINAHL (1982 to 2 May 2012).
The following search strategy was used in CENTRAL and modified appropriately for other databases:
#1 MeSH descriptor Oxazolidinones explode all trees
#2 MeSH descriptor Oxazolone explode all trees
#3 (linezolid* or oxazolone*):ti,ab,kw
#4 MeSH descriptor Glycopeptides explode all trees
#5 (vancomycin* or glycopeptide*):ti,ab,kw
#6 (#1 OR #2 OR #3 OR #4 OR #5)
#7 MeSH descriptor Soft Tissue Infections explode all trees
#8 MeSH descriptor Staphylococcal Skin Infections explode all trees
#9 MeSH descriptor Cellulitis explode all trees
#10 MeSH descriptor Erysipelas explode all trees
#11 MeSH descriptor Furunculosis explode all trees
#12 MeSH descriptor Abscess explode all trees
#13 MeSH descriptor Wound Infection explode all trees
#14 MeSH descriptor Fasciitis, Necrotizing explode all trees
#15 MeSH descriptor Myositis explode all trees
#16 MeSH descriptor Gas Gangrene explode all trees
#17 (soft NEXT tissue NEXT infection* or skin NEXT infection*):ti,ab,kw
#18 (cellulitis or erysipelas or furuncul* or abscess* or absess* or "necrotizing fasciitis" or myositis or "gas gangrene"):ti,ab,kw
#19 (wound* NEAR/2 infect*):ti,ab,kw
#20 (#7 OR #8 OR #9 OR #10 OR #11 OR #12 OR #13 OR #14 OR #15 OR #16 OR
#17 OR #18 OR #19)
#21 (#6 AND #20)
The search strategies for Ovid MEDLINE, Ovid EMBASE and EBSCO CINAHL can be found in Appendix 2. We combined the Ovid MEDLINE search with the Cochrane Highly Sensitive Search Strategy for identifying randomized trials in MEDLINE: sensitivity- and precision-maximizing version (2008 revision) (Lefebvre 2011). The Ovid EMBASE and EBSCO CINAHL searches were combined with the trial filters developed by the Scottish Intercollegiate Guidelines Network (SIGN) (SIGN 2008). There were no restrictions with respect to language, date of publication or study setting.
Searching other resources
We also contacted Pharmacia, Pfizer Pharmaceuticals in China for details of unpublished and ongoing trials. We scrutinised citations within all identified trials and major review articles to identify any additional trials.
Data collection and analysis
Selection of studies
Two review authors (YJ and YM) independently scanned the title, abstract and keywords of every record retrieved to determine which studies required further assessment. Full articles were retrieved when the information given in the titles, abstracts and keywords suggest the possibility that:
- The study compared linezolid and vancomycin (with or without co-interventions).
- The study had a prospective design.
If, after scanning the titles and abstracts, there was any doubt regarding these criteria, we retrieved the full article for clarification. We resolved disagreement by discussion with a third review author (BD), where necessary.
Data extraction and management
Two review authors (YJ and YM) independently extracted data using a standard data extraction form specifically adapted for this review. The data extraction form included the following details:
- General information: whether the paper was published or unpublished, title, authors, country of study, contact address, year of study, language of publication, year of publication, sponsor or funding organisation, setting.
- Methodological details: including criteria for risk of bias assessment (see below).
- Intervention: descriptions of dose, route, and timing of linezolid and vancomycin, with descriptions of dose, route, and timing of co-medication(s).
- Participants: inclusion and exclusion criteria, total number recruited and numbers in comparison groups, sex, age, baseline characteristics, withdrawals and losses to follow-up with reasons and descriptions, subgroups.
- Outcomes: clinical cure, microbiological cure, SSTI-related and treatment-related mortality, adverse events, duration of treatment, duration of hospitalisation and costs.
If information regarding data was unclear, we attempted to contact the authors of the original study reports to provide further details. When more than one publication related to the same study, we extracted data from all relevant publications, but did not duplicate the data.
Assessment of risk of bias in included studies
Two review authors (YJ andYM) independently assessed each included study using the Cochrane Collaboration tool for assessing risk of bias (Higgins 2011a). This tool addresses six specific domains, namely sequence generation, allocation concealment, blinding, incomplete outcome data, selective outcome reporting and other issues (e.g. baseline imbalances) (see Appendix 3 for details of criteria on which the judgements were based). Blinding and completeness of reporting of outcome data were assessed for each outcome separately. We completed a risk of bias table for each eligible study. We discussed any disagreements amongst all review authors to achieve a consensus.
We presented the assessment of risk of bias using a 'risk of bias summary figure', which presents all of the judgments in a cross-tabulation of study by entry. This display of internal validity indicates the weight the reader may give the results of each study.
Measures of treatment effect
We presented dichotomous outcomes (e.g. clinical cure, microbiological cure, adverse events, mortality) as risk ratios (RR) with corresponding 95% confidence intervals (CI). For statistically significant effects (primary outcomes), we calculated number the needed to treat (NNT) from the risk difference (RD).
We presented continuous data (e.g. duration of hospitalisation, duration of treatment, and costs) as mean differences (MD) with corresponding 95% CI.
Unit of analysis issues
Comparisons that randomise or allocate clusters (e.g. clinics) but do not account for clustering during analysis have potential unit of analysis errors resulting in artificially low P values and over-narrow confidence intervals. We decided to attempt to re-analyse studies with potential unit of analysis errors by calculating effective sample sizes, where possible (Higgins 2011b). If a comparison was re-analysed, then the P value was to be quoted and annotated as "re-analysed". If this was not possible, we would report only the point estimate (Donner 2001). If trials included multiple intervention groups receiving a complex intervention as defined above, we would spit the shared control group into two or more groups with smaller sample sizes, depending on the number of interventions studied, and include two or more comparisons (Higgins 2011b).
Dealing with missing data
When data were missing from the trial reports, we attempted to contact the trial authors to request these values. If this was not successful, we conducted intention-to-treat (ITT) analysis for all dichotomous outcomes (e.g. clinical cure, microbiological cure, adverse events, mortality). We analysed data on an endpoint basis for continuous outcomes (e.g. duration of hospital stay, duration of treatment, and costs), including only those participants for whom a final data point measurement was obtained (available case analysis). If the standard deviation (SD) was missing, and when the standard error (SE) was available, we imputed the SD from the SE using the formula SD = SE x N
Assessment of heterogeneity
Population, methodology, intervention and outcome measures for each study were assessed for clinical heterogeneity to see if pooling of results was feasible. Assessment for heterogeneity was carried out using the chi-squared test, with significance set at P value less than 0.1. In addition I
Assessment of reporting biases
If enough studies were identified, funnel plot analysis would have be enperformed to check for publication bias.
We pooled results following assessment for statistical heterogeneity as described above. Statistical analysis was performed in accordance with the guidelines for statistical analysis in the Cochrane Handbook for Systematic Reviews of Interventions (Deeks 2011). We conducted a narrative review of eligible studies if there was only one trial or the I
Subgroup analysis and investigation of heterogeneity
To assess whether the treatment effect is modified by clinical and demographic variables, we undertook subgroup analyses as follows:
- Children (younger than 18 years) and adults (18 years or older).
- Uncomplicated SSTIs and complicated SSTIs.
- MRSA subset.
If a sufficient number of trials were found, sensitivity analysis would be done to assess the robustness of the results as follows:
- Exclusion of studies with inadequate concealment of allocation.
- Exclusion of studies in which outcome evaluation was not blinded.
Description of studies
Results of the search
In total, we retrieved 505 articles through searching electronic databases; 11 articles were excluded because they were duplicates, and 468 were excluded after reading the abstracts and applying our inclusion criteria. The full text of the remaining 26 articles was reviewed, and 18 met the inclusion criteria for the review. Of these, thirteen articles were multiple publications, in which nine articles relate to four trials (Lin 2008; Stevens 2002; Weigelt 2005; Yogev 2003). Other five papers (Itani 2010; Jaksic 2006; Kohno 2007;Sharpe 2005; Wilcox 2009) were not multiple publications and referred to one trial each. Finally nine RCTs were included in the review (Figure 1).
|Figure 1. Study flow diagram.|
Nine RCTs were included in the review (Itani 2010; Jaksic 2006; Kohno 2007; Lin 2008; Sharpe 2005; Stevens 2002; Weigelt 2005; Wilcox 2009; Yogev 2003). Four of these nine RCTs evaluated SSTIs as the only type of infection (Itani 2010; Sharpe 2005; Weigelt 2005; Yogev 2003); four evaluated mixed infections and included types of infection other than SSTIs, such as bacteraemia of unknown source, pneumonia, and urinary tract infections (Jaksic 2006; Kohno 2007; Lin 2008; Stevens 2002); and one evaluated central venous, pulmonary artery, or arterial catheter-related infection with a subset of SSTIs (Wilcox 2009).
Characteristics of studies
All RCTs were parallel-group studies: two trials were randomised in a 2:1 ratio (Kohno 2007; Yogev 2003); one was a single-centre RCT located in the USA (Sharpe 2005), another was a multicentre RCT located in Japan (Kohno 2007); and a third was a multicentre RCT located in China (Lin 2008). The remaining six RCTs were multinational studies (Itani 2010; Jaksic 2006; Stevens 2002; Weigelt 2005; Wilcox 2009; Yogev 2003). The duration of follow-up ranged from 28 to 42 days.
Characteristics of patients
A total of 4496 participants were randomised, 3114 of whom had SSTIs. The subgroup data for SSTIs were obtained from trial reports; all were complicated SSTIs. Four RCTs reported the types of SSTIs (Itani 2010; Sharpe 2005; Weigelt 2005; Yogev 2003): abscess and infected skin ulcer was the most common infection (39.7%), followed by cellulitis (35.6%) and surgical wound infection (24.7%). Five trials enrolled people with MRSA infections (Itani 2010; Kohno 2007; Sharpe 2005; Stevens 2002; Weigelt 2005), while four trials enrolled people with Gram-positive bacterial infection (Jaksic 2006; Lin 2008; Wilcox 2009; Yogev 2003).
One RCT included children younger than 12 years old, with a mean age of 3.25 years (Yogev 2003). Five RCTs included adults (aged 18 years or over) with a mean age of 59.7 years (Itani 2010; Kohno 2007; Lin 2008; Sharpe 2005; Weigelt 2005). The remaining three RCTs included mixed populations over the age of 13 years, with a mean age of 54.4 years (Jaksic 2006; Stevens 2002; Wilcox 2009).
All RCTs included both males and females. A larger proportion of males was recruited, and they constituted 58.9% of all randomised patients. Only one RCT recruited more females than males, at 67% (Sharpe 2005).
Study treatment details
The doses of each drug were similar in all trials. In the RCTs with participants 13 years old or older, 600 mg linezolid was given as either an intravenous injection (IV) or orally every 12 hours whilst 1000 mg vancomycin was given IV every 12 hours except one RCT(Itani 2010) in which patients were randomised to receive oral or intravenous linezolid 600 mg every 12 hours, or intravenous vancomycin 15 mg/kg mg every 12 hours with dose adjustment as necessary, based on trough levels and creatinine clearance. The route of linezolid administration was IV in two RCTs (Jaksic 2006; Lin 2008); IV followed by oral administration in six RCTs (Itani 2010; Kohno 2007; Stevens 2002; Weigelt 2005; Wilcox 2009; Yogev 2003); and oral in only one RCT (Sharpe 2005). One RCT that enrolled participants under the age of 12 years (Yogev 2003), gave participants 10 mg/kg IV linezolid every eight hours or 10 to 15 mg/kg vancomycin every six to 24 hours according to age-dosing guidelines. People with concomitant presumed Gram-negative or mixed infections were treated with appropriate regimens, mainly aztreonam and aminoglycoside. The two groups had equal access to such co-interventions.
Eight studies were excluded after assessment of the full-text. Reasons for exclusion were:
Risk of bias in included studies
|Figure 2. Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.|
|Figure 3. Risk of bias summary: review authors' judgements about each risk of bias item for each included study.|
Sequence generation was unclear in all included studies.
Allocation concealment was unclear in two RCTs (Jaksic 2006; Lin 2008). The treatment allocation was not concealed in the remaining seven studies (Itani 2010; Kohno 2007; Sharpe 2005; Stevens 2002; Weigelt 2005; Wilcox 2009; Yogev 2003).
Overall there was high risk of selection bias.
The participants were blinded in Jaksic 2006 for all reported outcomes. Lin 2008 only reported that the study was "double-blind", but did not report details about who was blinded. The other seven RCTs were not blinded (Itani 2010; Kohno 2007; Sharpe 2005; Stevens 2002; Weigelt 2005; Wilcox 2009; Yogev 2003).
Two RCTs did not report whether outcome assessors were blinded (Jaksic 2006; Lin 2008). The outcome assessors in the other seven RCTs were not blinded (Itani 2010; Kohno 2007; Sharpe 2005; Stevens 2002; Weigelt 2005; Wilcox 2009; Yogev 2003).
Overall, the only two trials that reported being "double-blind' were small, and contributed to two primary analyses. Most of the trials did not undertake blinding, and so are at high risk of performance and detection bias.
Incomplete outcome data
Two RCTs (Itani 2010; Sharpe 2005) did not undertake ITT analyses. Seven RCTs (Jaksic 2006; Kohno 2007; Lin 2008; Stevens 2002; Weigelt 2005; Wilcox 2009; Yogev 2003) reported that an ITT analysis was performed. After looking at the full text of the potential seven trials and comparing the data reported at the beginning of randomisation with the data included in the analysis, however, we found that there were discrepancies between baseline data and final analysis which indicated that ITT had not been performed. So we assumed that none of the included trials undertook ITT analyses. Clinical cure and microbiological cure were reported by all studies, other outcomes were reported by some of the trials. We contact the authors requesting these data, but, to date, have received no reply.
Clinical and microbiological cure
All RCTs reported clinical and microbiological cure. Two trials, in which incomplete outcome data were adequately addressed, were judged to be at low risk of bias (Lin 2008; Weigelt 2005). Another two studies reported dropouts only for MRSA infections, but it was not clear how many dropouts were from the SSTIs subset, so we judged the trials to be at unclear risk of bias (Jaksic 2006; Stevens 2002). The remaining five RCTs did not report reasons or the numbers of dropouts, and were judged to be at high risk of bias.
SSTI-related and treatment-related mortality
No RCT reported SSTI-related and treatment-related mortality. Five RCTs reported all-cause mortality (Itani 2010; Jaksic 2006; Weigelt 2005; Wilcox 2009; Yogev 2003). Of these, three trials reported mortality in SSTI patients (Itani 2010; Weigelt 2005; Yogev 2003), while the other two reported mortality in mixed populations (Jaksic 2006; Wilcox 2009). Mortality data relating to the SSTI groups could not be extracted.
Three RCTs evaluated drug-related adverse events in SSTI participants (Itani 2010; Weigelt 2005; Yogev 2003); one RCT did not report adverse events (Sharpe 2005); while the remaining five RCTs reported adverse events of mixed infection types such as bacteraemia, pneumonia, and urinary tract infections (Kohno 2007; Lin 2008; Jaksic 2006; Stevens 2002; Wilcox 2009). We contacted the study authors for data relating to the SSTI subsets, but have not yet received a response.
Duration of hospital stay
Duration of treatment
Seven RCTs reported the duration of treatment (Itani 2010; Jaksic 2006; Kohno 2007; Lin 2008; Stevens 2002; Weigelt 2005; Wilcox 2009), but only two RCTs specifically reported the results for the subsets of SSTI patients (Itani 2010; Weigelt 2005).
Overall, two of the nine RCTs adequately addressed incomplete outcome data, and had a low dropout rate (Lin 2008; Weigelt 2005). In addition, although some of the included studies reported that they undertook ITT analyses, this was not confirmed by the data presented and, therefore, we have judged them to be at high risk of attrition bias.
We found the protocol for one RCT (Itani 2010); all of the primary and secondary outcomes pre-specified in the protocol were subsequently reported, and, accordingly, the trial was judged to be at low risk of bias for this domain. We searched, but did not find the protocols for the other included trials, and so the remaining eight RCTs were judged to be at unclear risk of bias.
Other potential sources of bias
There were baseline imbalances in two trials: in Stevens 2002, participants in the linezolid group were significantly older than those in the vancomycin group (63.9 versus 59.8 years; P value 0.0157), while in Sharpe 2005, patients in the linezolid group were significantly younger than those in the vancomycin group (66 versus 76 years). These two trials were judged to be at an high risk of bias for this domain.
Effects of interventions
Linezolid compared with vancomycin (nine RCTs)
Eight RCTs that reported outcomes in adult or mixed populations (Itani 2010; Jaksic 2006; Kohno 2007; Lin 2008; Sharpe 2005; Stevens 2002; Weigelt 2005; Wilcox 2009), and one RCT that reported outcomes in children (Yogev 2003), were included for this outcome. In total, 3114 participants with SSTIs were randomised in nine RCTs. We conducted ITT analysis for all randomised participants. We coded indeterminate outcomes and missing data as "no cure". Pooling of the nine trials demonstrated a statistically significant difference in cure rate of SSTIs in favour of linezolid (RR 1.09, 95% CI 1.03 to 1.16; I
The meta-analysis to evaluate the microbiological cure rate included 2014 SSTI participants from all nine trials with a positive culture at baseline. More SSTIs achieved microbiological cure when treated with linezolid than with vancomycin (RR 1.08, 95% CI 1.01 to 1.16; I
SSTI-related and treatment-related mortality
No RCT reported SSTI-related or treatment-related mortality. Three RCTs (2352 participants) reported all-cause mortality of SSTI patients (Itani 2010; Weigelt 2005; Yogev 2003), and found there was no significant difference in all-cause mortality between linezolid and vancomycin (RR 1.44, 95% CI 0.75 to 2.80; I
One trial (726 participants) reported adverse events including events related, or unrelated, to treatment (Wilcox 2009). Seven trials (3710 participants) reported data on treatment-related adverse events (Itani 2010; Jaksic 2006; Kohno 2007; Lin 2008; Stevens 2002; Weigelt 2005; Yogev 2003). One trial (60 participants) did not mention adverse events (Sharpe 2005).
Three RCTs evaluated adverse events in SSTI participants and were included in the meta-analysis (Itani 2010; Weigelt 2005; Yogev 2003), while the other five RCTs reported data on adverse effects for a variety of infection types, such as bacteraemia, pneumonia, and urinary tract infections, so that data relating to SSTIs could not be extracted (Kohno 2007; Lin 2008; Jaksic 2006; Stevens 2002; Wilcox 2009).
Fewer people in the linezolid group had red man syndrome (two RCTs, 1172 patients; RR 0.04, 95% CI 0.01 to 0.29; I
More people in the linezolid group had thrombocytopenia (two RCTs, 1300 patients; RR 13.06, 95% CI 1.72 to 99.22; I
No differences were reported for anaemia (two RCTs,1300 patients; RR 0.73, 95% CI 0.33 to 1.62; I
Duration of hospital stay
Four RCTs (2522 participants) reported the duration of hospital stay (Itani 2010; Sharpe 2005; Stevens 2002; Weigelt 2005), but reported only the mean days and P value. Itani 2010 showed that in the linezolid group, the median and mean lengths of stay (LOS) were 5.0 and 7.7 days, respectively, compared with 7.0 and 8.9 days, respectively, in the vancomycin group (P value 0.016). Sharpe 2005 reported that the median LOS was three days shorter with linezolid (P value 0.003). Stevens 2002 reported that LOS was five days shorter for the linezolid group than the vancomycin group (9 versus 14 days, P value 0.052) among patients with SSTI. Weigelt 2005 found that the mean all cause total LOS was significantly shorter in the linezolid arm (7.4 versus 9.8 days, P value less than 0.0001).
Duration of treatment
Seven RCTs (4316 participants) reported the treatment duration (Itani 2010; Jaksic 2006; Kohno 2007; Lin 2008; Stevens 2002; Weigelt 2005; Wilcox 2009), but only two reported results for the subset of SSTI patients (Itani 2010; Weigelt 2005). Itani 2010 reported only the mean days and P value. The mean duration of intravenous therapy was reported as being significantly shorter in the linezolid group than the vancomycin group (5.3 versus 9.8 days; P value 0.001). For Weigelt 2005, however, the mean treatment duration was longer for the linezolid group than for the vancomycin group (MD 0.90 days, 95% CI 0.32 to 1.48; Analysis 5.1).
Two RCTs (1240 participants) reported the treatment cost (Sharpe 2005; Weigelt 2005), but Sharpe 2005 did not report the SD or SE.The daily cost of outpatient therapy was USD 97 less with oral linezolid than with intravenous vancomycin (USD 103 versus USD 200, P value less than 0.001). Medication charges per day for inpatient linezolid treatment were USD 117 more than those for inpatient vancomycin (USD 277 versus USD 160, P value 0.069). However, the median length of hospital stay was three days shorter with linezolid (P value 0.003). Thus, with linezolid treatment, an average of USD 6438 in total hospital charges per patient was avoided (Sharpe 2005). Weigelt 2005 found that mean cost (plus or minus SD) for treatIing with linezolid was less than for vancomycin; that is, USD 4865 plus or minus USD 4367 compared with USD 5738 plus or minus USD 5190, respectively (P value 0.017).
1. Children (under 18 years) and adults (18 years or over)
There was only one study (120 participants) in children (Yogev 2003), though five RCTs (2402 participants) included adults (18 years or over) with SSTI (Itani 2010; Kohno 2007; Lin 2008; Sharpe 2005; Weigelt 2005). The remaining three RCTs (592 participants) included mixed populations (13 years and over) with SSTI (Jaksic 2006; Stevens 2002; Wilcox 2009). In children, there was no statistically significant difference for either clinical cure (RR 1.14; 95% CI 0.91 to 1.44) or microbiological cure (RR 1.08; 95% CI 0.90 to 1.31). In adults (18 years and over), there was a statistically significant difference in favour of linezolid for both clinical cure (RR 1.16; 95% CI 1.02 to 1.32; I
2. Uncomplicated SSTIs and complicated SSTIs
No trial reported uncomplicated SSTIs. This meant that there were insufficient data to permit this subgroup analysis.
3. MRSA subset
Five RCTs (2570 participants) enrolled people with MRSA infections (Itani 2010; Kohno 2007; Sharpe 2005; Stevens 2002; Weigelt 2005). One RCT enrolled people with Gram-positive bacterial infection, but reported data of MRSA as a subset (89 participants) (Wilcox 2009). Thus, six RCTs reported the clinical and microbiological cure rate of MRSA infections. Clinical cure was evaluated in the people who were suspected or proven to have MRSA infections (2659 participants), while microbiological cure rate was evaluated for the people who had a positive MRSA culture at baseline (1289 participants). The results showed that linezolid achieved both a significantly better clinical cure rate (RR 1.09, 95% CI 1.03 to 1.17; I
1. Exclusion of studies with inadequate concealment of allocation
Allocation concealment was unclear in all included RCTs and, therefore, this analysis was not undertaken.
2. Exclusion of studies in which outcome evaluation was not blinded
Only two of the nine included trials had a blinded design (Jaksic 2006; Lin 2008). After removal of the studies in which outcome evaluation was not blinded, there was no difference in treatment success for clinical cure for patients (RR 1.22, 95% CI 0.97 to 1.53), or for microbiological cure for patients (RR 1.08, 95% CI 0.85 to 1.38). There was no blinding for any other outcome for the RCTs, so there were insufficient data to perform the planned sensitivity analyses.
Summary of main results
This review evaluated the effects and safety of linezolid compared with vancomycin for the treatment of people with skin and soft tissue infections (SSTIs). Of the 26 studies initially identified, nine (with 18 citations) were included in the review.
In summary, the included RCTs were of poor methodological quality, with high risk of bias, which weakens the confidence that can be placed on the individual and pooled results. The results of our review suggest that linezolid was more effective than vancomycin for treatment of SSTIs. Linezolid treatment was associated with a better clinical cure rate (RR 1.09, 95% CI 1.03 to 1.16), and better microbiological cure rate (RR 1.08, 95% CI 1.01 to 1.16). There was no significant difference in mortality between linezolid and vancomycin (RR 1.44, 95% CI 0.75 to 2.80). The linezolid group had a lower incidence of red man syndrome (RR 0.04, 95% CI 0.01 to 0.29), pruritus (RR 0.36, 95% CI 0.17 to 0.75), and rash (RR 0.27, 95% CI 0.12 to 0.58) than vancomycin. The linezolid group, however, had a greater incidence of thrombocytopenia (RR 13.06, 95% CI 1.72 to 99.22), and nausea (RR 2.45, 95% CI 1.52 to 3.94). We undertook subgroup analyses in people who had MRSA infections and found that linezolid was more effective than vancomycin in achieving a clinical cure (RR 1.09, 95% CI 1.03 to 1.17) and a microbiological cure (RR 1.17, 95% CI 1.04 to 1.32). We also undertook subgroup analyses in children (under 18 years of age) and adults (18 years and over). In children, there was no statistically significant difference for clinical cure and microbiological cure (one RCT Yogev 2003). In adults (18 years and over), there was a statistically significant difference in favour of linezolid for both clinical cure (RR 1.16; 95% CI 1.02 to 1.32) and microbiological cure (RR 1.17; 95% CI 1.02 to 1.34).The lengths of stay in hospital were shorter for the linezolid group than the vancomycin group. The daily cost of outpatient therapy was less with oral linezolid than with intravenous vancomycin. Although inpatient treatment with linezolid cost more than inpatient treatment with vancomycin per day, the median length of hospital stay was three days shorter with linezolid. Thus, total hospital charges per patient was less with linezolid treatment than with vancomycin treatment.
Overall completeness and applicability of evidence
The outcomes reported in the trials focused on clinical and microbiological cure. Economics of health, such as duration of hospital stay, treatment duration and cost were reported in only a few RCTs. Four RCTs reported the duration of hospital stay (Itani 2010; Sharpe 2005; Stevens 2002; Weigelt 2005), but they only reported the mean days and P value. Only two RCTs reported results for subsets of SSTI patients (Itani 2010; Weigelt 2005). The duration of intravenous treatment was shorter for patients treated with linezolid in Itani 2010, however, it was longer in Weigelt 2005. Two trials reported the treatment cost (Sharpe 2005; Weigelt 2005).
No RCT reported SSTI-related and treatment-related mortality, and only three reported all-cause mortality and adverse effects for the subset of SSTI patients (Itani 2010; Weigelt 2005; Yogev 2003). Other RCTs reported the outcome for a pooled population of patients with mixed infection types, but, as we know, potential differences in mortality and adverse effects may exist within these different infection types. Unless individual subsets of patients were investigated, this result could not reflect mortality or adverse events specifically for SSTIs.
Six of the nine included trials were multinational studies (Itani 2010; Jaksic 2006; Stevens 2002; Weigelt 2005; Wilcox 2009; Yogev 2003); the remaining three were located in the USA (Sharpe 2005), Japan (Kohno 2007), and China (Lin 2008). Participants came from diverse cultural and geographic backgrounds, were of all ages, and both sexes were represented, therefore, this review is representative of different racial and regional groups.
Quality of the evidence
In general, all the trials were of poor methodological quality. Firstly, although all studies stated that randomisation was used, none mentioned the method of randomisation. Treatment allocation was not concealed in seven of the trials and it was unclear whether it had been in the remaining two RCTs. The lack of disclosure of the method of randomisation and the lack of allocation concealment in all included trials is concerning. Treatment effect may be overestimated by 30 to 40 per cent when allocation concealment is absent (Schulz 1995). Secondly, only two of the nine RCTs (with small sample sizes) had a blinded design (Jaksic 2006; Lin 2008), and lack of blinding might cause an overestimation of treatment effects.Thirdly, seven of the nine RCTs were either unclear about, or did not report dropout data, and none of them undertook an ITT analysis. The omission or non-reporting of these items may lead to, or indicate, attrition bias that may contribute to false positive or negative findings. Finally, all the trials were funded by the pharmaceutical company that produces linezolid. It should be noted that, while the pharmaceutical companies need to support research in an ethical manner, pharmaceutical funding may introduce publication bias and, in this case, might overestimate the effects of linezolid.
Potential biases in the review process
1. We could not perform a funnel plot to investigate publication bias in this systematic review due to the small numbers of trials. Thus, one of our concerns is the potential for publication bias. The pharmaceutical company that produces linezolid funded all nine of the included trials in this review, which might mean that positive results are more likely to be reported than negative ones. Previously an association between positive results and publication has been demonstrated (Dickersin 1990), which may have identified a potential source of bias that, in this case, could have led to an overestimation of the treatment effect.
2. All RCTs excluded patients with severe SSTIs, such as necrotising fasciitis, gas gangrene, and infected burns, therefore, the effects of linezolid or vancomycin for such severe infections could not be estimated.
3. We undertook subgroup analysis for MRSA-infected SSTIs. Two potential biases need to be considered: firstly, when a person presents with a SSTI, the identity of the infecting pathogen is usually not known. Whilst, for the outcome of clinical cure, it was suspected that the participants had MRSA-infected SSTIs, MRSA can only be identified after culture. Secondly, although testing for microbiological eradication may provide definitive confirmation that the MRSA SSTI has been resolved, use of this endpoint is confounded by people who have natural colonisation of MRSA. This may be a potential source of bias, as it could have led to an underestimate of the treatment effect. Hence, clinicians should consider both the clinical and microbiological cure as indicators of treatment response.
4. The heterogeneity in this review was somewhat high for five outcomes. Possible reasons for this could include the lack of concealment of allocation, failure to perform an intention-to-treat analysis, and underlying patient characteristics such as different types of SSTIs and age.
5. After removal of the trials in which outcome assessment was not blinded, there were only two trials (Jaksic 2006; Lin 2008). Sensitivity analyses showed no difference in treatment success for clinical or microbiological cure. This may be due to the small sample sizes of the trials included (109 participants).
Agreements and disagreements with other studies or reviews
Our results are in agreement with some studies. Worldwide clinical trials with linezolid have demonstrated that linezolid has significantly better clinical and microbiological cure rates than vancomycin in people with pneumonia (Kollef 2004; Wunderink 2003). There also are some reviews which have favoured linezolid.: one meta-analysis evaluated the clinical and microbiological outcomes of linezolid compared with vancomycin in MRSA complicated SSTIs (Bounthavong 2010): it reported that resolution of infection favoured the use of linezolid over vancomycin (OR 1.41; 95% CI: 1.03 to 1.95), and that microbiological eradication in MRSA patients consistently favoured the use of linezolid (OR 2.90; 95% CI: 1.90 to 4.41). Another meta-analysis also demonstrated that linezolid was more effective than vancomycin (OR 1.40, 95% CI 1.01 to 1.95) in people with SSTIs (Beibei 2010). For adverse effects, both reviews found that people treated with linezolid had higher proportions of thrombocytopenia, and a higher proportion of people treated with vancomycin had renal insufficiency. No difference in mortality was reported between the two antibiotics. Nonetheless, these reviews have limitations: they assessed mortality and adverse effects using mixed data, whilst data due to SSTIs could not be extracted. As we know, the mortality and side effects of SSTIs may not be the same as with other infections. For example, the mortality for bacteraemia is higher than for SSTIs. Secondly, some RCTs we identified and included in this review were not included in the earlier reviews (Itani 2010; Jaksic 2006; Sharpe 2005).
Despite this, our results are inconsistent with some other reviews. One review compared the effects of linezolid with vancomycin for the treatment of MRSA SSTIs in hospital inpatients (Dodds 2009). This review included four trials with a total of 174 participants for clinical outcomes and 439 participants for microbiological outcomes, respectively (Sharpe 2005; Stevens 2002; Weigelt 2005; Yogev 2003). There was no significant effect for clinical outcomes (RR 0.34; 95% CI 0.04 to 2.89) or microbiological outcomes (RR 0.55; 95% CI 0.30 to 1.01). Another review compared linezolid with vancomycin (Shorr 2005), and concluded that linezolid was not inferior to vancomycin in patients with secondary S aureus bacteraemia (five RCTs; 144 adults with S aureus bacteraemia). These two reviews were small, which may be a possible cause of these inconsistencies.
Implications for practice
The poor quality evidence contained within this systematic review shows that linezolid seems to be more effective than vancomycin for the treatment of patients with SSTIs and SSTIs caused by MRSA. The lengths of stay in hospital were shorter, and the costs of treatment were lower, for people in the linezolid group compared to the vancomycin group. Fewer people in the linezolid group suffered from red man syndrome, pruritus and rash compared with vancomycin, but more people in the linezolid group suffered from thrombocytopenia and nausea. In spite of these results, the evidence may be limited by potential biases, so further evidence from higher quality trials is necessary before definite conclusions can be drawn.
Implications for research
Further well-designed and reported randomised controlled trials are needed to confirm the available evidence. The following features should be addressed in future studies:
We would like to thank the following peer referees for their helpful comments on the review: Julie Bruce, Susan O’Meara, Ruth Foxlee, Jane Burch, Elmer Villanueva, Beryl de Souza, Brian Gilchrist, Patricia Davies, Shirley Manknell. Sally Bell-Syer is especially acknowledged for language assistance, and Nicola Thomis for her contributions to the glossary. We also would like to acknowledge the copy editor, Elizabeth Royle, for edits to our draft.
Data and analyses
- Top of page
- Authors' conclusions
- Data and analyses
- Contributions of authors
- Declarations of interest
- Sources of support
- Differences between protocol and review
- Index terms
Appendix 1. Glossary
Appendix 2. Search strategies for Ovid Medline, Ovid Embase and EBSCO CINAHL
1 exp Oxazolidinones/ (3454)
2 exp Oxazolone/ (471)
3 (linezolid$ or oxazolone$).ti,ab. (3313)
4 or/1-3 (5205)
5 exp Glycopeptides/ (24374)
6 (vancomycin$ or glycopeptide$).ti,ab. (14989)
7 or/5-6 (32269)
8 exp Soft Tissue Infections/ (1969)
9 exp Staphylococcal Skin Infections/ (2085)
10 exp Cellulitis/ (2621)
11 exp Erysipelas/ (360)
12 exp Furunculosis/ (298)
13 exp Abscess/ (17532)
14 exp Wound Infection/ (15200)
15 exp Fasciitis, Necrotizing/ (1891)
16 exp Myositis/ (6975)
17 exp Gas Gangrene/ (356)
18 (soft tissue infection$ or skin infection$).ti,ab. (4702)
19 (cellulitis or erysipelas or furuncul$ or abscess$ or absess$ or necrotizing fasciitis or myositis or gas gangrene or (wound$ adj2 infect$)).ti,ab. (44369)
20 or/8-19 (69951)
21 4 and 7 and 20 (216)
22 randomized controlled trial.pt. (247475)
23 controlled clinical trial.pt. (40136)
24 randomized.ab. (201843)
25 placebo.ab. (93559)
26 clinical trials as topic.sh. (80952)
27 randomly.ab. (138890)
28 trial.ti. (75242)
29 or/22-28 (558737)
30 Animals/ (2530681)
31 Humans/ (7027945)
32 30 not 31 (1649878)
33 29 not 32 (508211)
34 21 and 33 (43)
1 exp Oxazolidinone Derivative/ (2611)
2 exp Oxazolone/ (956)
3 exp Linezolid/ (10231)
4 (linezolid$ or oxazolone$).ti,ab. (5207)
5 or/1-4 (13224)
6 exp Vancomycin/ (43322)
7 exp Vancomycin Derivative/ (216)
8 exp Glycopeptide/ (5164)
9 (vancomycin$ or glycopeptide$).ti,ab. (22171)
10 or/6-9 (51486)
11 exp Soft Tissue Infection/ (5340)
12 exp Skin Infection/ (77395)
13 exp Cellulitis/ (8532)
14 exp Erysipelas/ (1406)
15 exp Furunculosis/ (857)
16 exp Abscess/ (41568)
17 exp Wound Infection/ (19807)
18 exp Necrotizing Fasciitis/ (3450)
19 exp Myositis/ (15627)
20 exp Gas Gangrene/ (680)
21 (soft tissue infection$ or skin infection$).ti,ab. (7434)
22 (cellulitis or erysipelas or furuncul$ or abscess$ or absess$ or necrotizing fasciitis or myositis or gas gangrene or (wound$ adj2 infect$)).ti,ab. (65393)
23 or/11-22 (178863)
24 5 and 10 and 23 (1789)
25 Clinical trial/ (715292)
26 Randomized controlled trials/ (29861)
27 Random Allocation/ (51197)
28 Single-Blind Method/ (15897)
29 Double-Blind Method/ (87219)
30 Cross-Over Studies/ (32445)
31 Placebos/ (169756)
32 Randomi?ed controlled trial$.tw. (82914)
33 RCT.tw. (10982)
34 Random allocation.tw. (931)
35 Randomly allocated.tw. (14603)
36 Allocated randomly.tw. (1227)
37 (allocated adj2 random).tw. (266)
38 Single blind$.tw. (9897)
39 Double blind$.tw. (92147)
40 ((treble or triple) adj blind$).tw. (248)
41 Placebo$.tw. (140349)
42 Prospective Studies/ (206934)
43 or/25-42 (1077729)
44 Case study/ (16788)
45 Case report.tw. (170882)
46 Abstract report/ or letter/ (519805)
47 or/44-46 (703087)
48 43 not 47 (1048538)
49 animal/ (730814)
50 human/ (8821758)
51 49 not 50 (489053)
52 48 not 51 (1026150)
53 24 and 52 (546)
S17 S16 and S4 and S1
S16 S15 or S14 or S13 or S12 or S11 or S10 or S9 or S8 or S7 or S6 or S5
S15 wound* N2 infection*
S14 cellulitis or erysipelas or furuncul* or abscess* or absess* or necrotizing fasciitis or myositis or gas gangrene
S13 soft tissue infection* or skin infection*
S12 (MH "Gas Gangrene")
S11 (MH "Myositis")
S10 (MH "Fasciitis, Necrotizing")
S9 (MH "Wound Infection+")
S8 (MH "Abscess+")
S7 (MH "Furunculosis")
S6 (MH "Cellulitis")
S5 (MH "Soft Tissue Infections")
S4 (S3 or S2)
S2 (MH "Vancomycin")
S1 linezolid* or oxazolone* or oxazolidinone*
Appendix 3. Assessment of risk of bias in included studies
1. Was the allocation sequence randomly generated?
Low risk of bias
The investigators describe a random component in the sequence generation process such as: referring to a random number table; using a computer random number generator; coin tossing; shuffling cards or envelopes; throwing dice; drawing of lots.
High risk of bias
The investigators describe a non-random component in the sequence generation process. Usually, the description would involve some systematic, non-random approach, for example: sequence generated by odd or even date of birth; sequence generated by some rule based on date (or day) of admission; sequence generated by some rule based on hospital or clinic record number.
Insufficient information about the sequence generation process to permit judgement of low or high risk of bias.
2. Was the treatment allocation adequately concealed?
Low risk of bias
Participants and investigators enrolling participants could not foresee assignment because one of the following, or an equivalent method, was used to conceal allocation: central allocation (including telephone, web-based and pharmacy-controlled randomisation); sequentially-numbered drug containers of identical appearance; sequentially-numbered, opaque, sealed envelopes.
High risk of bias
Participants or investigators enrolling participants could possibly foresee assignments and thus introduce selection bias, because allocation based on one of the following or an equivalent method: using an open random allocation schedule (e.g. a list of random numbers); assignment envelopes used without appropriate safeguards (e.g. if envelopes were unsealed or non-opaque or not sequentially numbered); alternation or rotation; date of birth; case record number; any other explicitly unconcealed procedure.
Insufficient information to permit judgement of low or high risk of bias. This is usually the case if the method of concealment is not described or not described in sufficient detail to allow a definite judgement, for example if the use of assignment envelopes is described, but it remains unclear whether envelopes were sequentially numbered, opaque and sealed.
3. Blinding - was knowledge of the allocated interventions adequately prevented during the study?
Low risk of bias
Any one of the following:
- No blinding, but the review authors judge that the outcome and the outcome measurement are not likely to be influenced by lack of blinding.
- Blinding of participants and key study personnel ensured, and unlikely that the blinding could have been broken.
- Either participants or some key study personnel were not blinded, but outcome assessment was blinded and the non-blinding of others is unlikely to introduce bias.
High risk of bias
Any one of the following:
- No blinding or incomplete blinding, and the outcome or outcome measurement is likely to be influenced by lack of blinding.
- Blinding of key study participants and personnel attempted, but likely that the blinding could have been broken.
- Either participants or some key study personnel were not blinded, and the non-blinding of others is likely to have introduced bias.
Either of the following:
- Insufficient information to permit judgement of low or high risk of bias.
- The study did not address this outcome.
4. Were incomplete outcome data adequately addressed?
Low risk of bias
Any one of the following:
- No missing outcome data.
- Reasons for missing outcome data unlikely to be related to true outcome (for survival data, censoring unlikely to be introducing bias).
- Missing outcome data balanced in numbers across intervention groups, with similar reasons for missing data across groups.
- For dichotomous outcome data, the proportion of missing outcomes compared with the observed event risk was not enough to have a clinically relevant impact on the intervention effect estimate.
- For continuous outcome data, plausible effect size (difference in means or standardised difference in means) among missing outcomes was not enough to have a clinically relevant impact on observed effect size.
- Missing data have been imputed using appropriate methods.
High risk of bias
Any one of the following:
- Reason for missing outcome data likely to be related to true outcome, with either imbalance in numbers, or reasons for missing data across intervention groups.
- For dichotomous outcome data, the proportion of missing outcomes compared with the observed event risk was enough to induce clinically relevant bias in intervention effect estimate.
- For continuous outcome data, plausible effect size (difference in means or standardised difference in means) among missing outcomes was enough to induce clinically relevant bias in observed effect size.
- 'As-treated' analysis done with substantial departure of the intervention received from that assigned at randomisation.
- Potentially inappropriate application of simple imputation.
Either of the following:
- Insufficient reporting of attrition/exclusions to permit judgement of low or high risk of bias (e.g. number randomised not stated, no reasons for missing data provided).
- The study did not address this outcome.
5. Are reports of the study free of suggestion of selective outcome reporting?
Low risk of bias
Either of the following:
- The study protocol is available and all of the study's pre-specified (primary and secondary) outcomes that are of interest in the review have been reported in the pre-specified way.
- The study protocol is not available, but it is clear that the published reports include all expected outcomes, including those that were pre-specified.
High risk of bias
Any one of the following:
- Not all of the study's pre-specified primary outcomes have been reported.
- One or more primary outcomes is reported using measurements, analysis methods or subsets of the data (e.g. subscales) that were not pre-specified.
- One or more reported primary outcomes were not pre-specified (unless clear justification for their reporting is provided, such as an unexpected adverse effect).
- One or more outcomes of interest in the review are reported incompletely so that they cannot be entered in a meta-analysis.
- The study report fails to include results for a key outcome that would be expected to have been reported for such a study.
Insufficient information to permit judgement of low or high risk of bias. It is likely that the majority of studies will fall into this category.
6. Other sources of potential bias
Low risk of bias
The study appears to be free of other sources of bias.
High risk of bias
There is at least one important risk of bias. For example, the study:
- had a potential source of bias related to the specific study design used; or
- had extreme baseline imbalance; or
- has been claimed to have been fraudulent; or
- had some other problem.
There may be a risk of bias, but there is either:
- insufficient information to assess whether an important risk of bias exists (e.g. baseline imbalances); or
- insufficient rationale or evidence that an identified problem will introduce bias.
Contributions of authors
Yue Jirong: conceived the review question; co-ordinated the protocol development; completed the first draft and edited the review.
Dong Birong: developed the review and advised on the review, co-ordinated the review development and performed part of writing and editing of the review, approved the final version of the review prior to submission and is guarantor.
Yang Ming: developed and edited the review and made an intellectual contribution to it.
Chen Xiaomei: conceived the review question, edited the review and made an intellectual contribution to it.
Wu Taixiang: developed the review, advised and performed part of writing and editing of the review, and made an methodological contribution.
Liu Guanjian: advised and performed part of writing and editing of the review, and made a statistical contribution.
Contributions of editorial base
Nicky Cullum: edited the review; advised on methodology, interpretation and review content.
Julie Bruce, Editor: approved the final review prior to submission.
Sally Bell-Syer: co-ordinated the editorial process. Advised on methodology, interpretation and content. Edited and copy edited the review.
Ruth Foxlee: designed the search strategy and edited the search methods section.
Declarations of interest
Sources of support
- Chinese Cochrane Center, China.
- NIHR/Department of Health (England), (Cochrane Wounds Group), UK.
Differences between protocol and review
- Under "Types of outcome measures/Primary outcomes" in the sentence "Proportion of patients or infections healed: healing is defined as either the resolution of all clinical signs and symptoms of infection, as assessed by laboratory test or as defined by trialists", we changed to, "clinical cure (resolution of symptoms and signs) and microbiological cure (eradication of bacteria on wound culture)." We think the meaning of the two statements is the same, however, "clinical/microbiological cure" is more concise and helpful than the original wording when used throughout the text of the review.
- In the section "Subgroup analysis and investigation of heterogeneity", we added:"3. MRSA subset", because MRSA is important for SSTIs. The morbidity and treatment costs associated with MRSA-infected SSTIs are higher than for other pathogen infections, so we added this subgroup analysis.
- We added some information in the "Background" section in line with comments from peer referees.
- We added some information in the "Methods/Dealing with missing data" section, in line with comments from peer referees.
Medical Subject Headings (MeSH)
Acetamides [adverse effects; *therapeutic use]; Anti-Bacterial Agents [adverse effects; *therapeutic use]; Drug Eruptions [etiology]; Length of Stay; Linezolid; Oxazolidinones [adverse effects; *therapeutic use]; Pruritus [chemically induced]; Randomized Controlled Trials as Topic; Skin Diseases, Bacterial [*drug therapy]; Soft Tissue Infections [*drug therapy]; Thrombocytopenia [chemically induced]; Vancomycin [adverse effects; *therapeutic use]
MeSH check words
* Indicates the major publication for the study