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QUOROM Guidelines for Meta-Analyses and Systematic Reviews of RCTs

QUOROM Guidelines for Meta-Analyses and Systematic Reviews of RCTs*
 
Title Identify the study as a meta-analysis (or systematic review) of RCTs
 
Abstract Use the journal’s structured format
 
Introduction Present
  • The clinical problem
  • The biological rationale for the intervention
  • The rationale for the review
  • An explicit statement of objectives which includes the study population, the condition of interest, the exposure or intervention, and the outcome(s) considered
 
Sources Describe
  • The information sources in detail (eg databases, registers, personal files, experts, agencies, hand-searching)
  • Any restriction (years considered, publication status, language of publication)
 
Study Selection Describe
  • Inclusion and exclusion criteria (defining population, intervention, main outcomes, and study design)
  • How clinical heterogeneity was assessed
  • Methods used for validity assessment
  • The criteria and process used for validity assessment (eg, masked conditions, quality assessment)
  • The data abstraction process (eg, completed independently, in duplicate)
  • Study characteristics and how clinical heterogeneity was assessed
  • The principal measures of effect (eg, relative risk)
  • Method of combining results (statistical testing and confidence intervals)
  • Handling of missing data
  • How statistical heterogeneity was assessed
  • Rationale for any a-priori sensitivity and subgroup analyses
 
Results Present
  • A meta-analysis profile summarizing trial flow
  • Descriptive data for each trial (study design, participant characteristics, sample size, details of intervention, outcome definitions, length of follow-up)
  • Agreement on the selection and validity assessment
  • Simple summary results (for each treatment group in each trial, for each primary outcome)
  • Data needed to calculate effect sizes and confidence intervals in intention-to-treat analyses
 
Discussion Discuss
  • Key findings
  • Clinical inferences based on internal and external validity
  • The results in light of the totality of available evidence
  • Strengths and weaknesses
  • Potential biases in the review process (eg, publication bias)
  • Future research agenda
*Modified from Moher D, Cook DJ, Eastwood S, Olkin I, Rennie D, Stroup DF. Improving the quality of reports of meta-analyses of randomised controlled trials: the QUOROM statement. Quality of Reporting of Meta-analyses. Lancet 1999;354:1896–900.



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