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Empirical evidence of bias in treatment effect estimates in controlled trials with different interventions and outcomes: meta-epidemiological study.

Authors :
Wood, Lesley
Egger, Matthias
Gluud, Lise Lotte
Schulz, Kenneth F
Juni, Peter
Altman, Douglas G
Gluud, Christian
Martin, Richard M
Wood, Anthony J G
Sterne, Jonathan A C
Source :
BMJ: British Medical Journal (International Edition). 3/15/2008, Vol. 336 Issue 7644, p601-605. 5p. 2 Charts.
Publication Year :
2008

Abstract

Objective To examine whether the association of inadequate or unclear allocation concealment and lack of blinding with biased estimates of intervention effects varies with the nature of the intervention or outcome. Design Combined analysis of data from three meta- epidemiological studies based on collections of meta- analyses. Data sources 146 meta-analyses including 1346 trials examining a wide range of interventions and outcomes. Main outcome measures Ratios of odds ratios quantifying the degree of bias associated with inadequate or unclear allocation concealment, and lack of blinding, for trials with different types of intervention and outcome. A ratio of odds ratios <1 implies that inadequately concealed or non- blinded trials exaggerate intervention effect estimates. Results In trials with subjective outcomes effect estimates were exaggerated when there was inadequate or unclear allocation concealment (ratio of odds ratios 0.69 (95% Cl 0.59 to 0.82)) or lack of blinding (0.75 (0.61 to 0.93)). In contrast, there was little evidence of bias in trials with objective outcomes: ratios of odds ratios 0.91 (0.80 to 1.03) for inadequate or unclear allocation concealment and 1.01 (0.92 to 1.10) for lackof blinding. There was little evidence for a difference between trials of drug and non- drug interventions. Except fortrials with all cause mortality as the outcome, the magnitude of bias varied between meta-analyses. Conclusions The average bias associated with defects in the conduct of randomised trials varies with the type of outcome. Systematic reviewers should routinely assess the risk of bias in the results of trials, and should report meta-analyses restricted to trials at low risk of bias either as the primary analysis or in conjunction with less restrictive analyses. INSET: WHAT IS ALREADY KNOWN ON THIS TOPIC. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09598146
Volume :
336
Issue :
7644
Database :
Academic Search Index
Journal :
BMJ: British Medical Journal (International Edition)
Publication Type :
Academic Journal
Accession number :
31478881
Full Text :
https://doi.org/10.1136/bmj.39465.451748.AD