A systematic survey showed important limitations in the methods for assessing drug safety among systematic reviews.
J Clin Epidemiol. 2020 Apr 01;:
Authors: Li L, Deng K, Busse JW, Zhou X, Xu C, Liu Z, Ren Y, Zou K, Sun X
OBJECTIVES: To examine the design, conduct, and analysis of systematic reviews assessing drug safety through a cross-sectional survey.
STUDY DESIGN AND SETTING: We searched PubMed to identity systematic reviews published in the Cochrane Database of Systematic Reviews and Core Clinical Journals indexed in 2015, and randomly sampled systematic reviews assessing drug effects at a 1:1 ratio of Cochrane and non-Cochrane reviews. Teams of two investigators independently conducted study screening and collected data, using pre-specified, standardized questionnaires. In addition to general information, we collected details about the planning and analyses of safety outcomes.
RESULTS: We included 120 systematic reviews, including 60 Cochrane and 60 non-Cochrane ones. Most reviews searched PubMed/MEDLINE (n=117, 97.5%), EMBASE (n=105, 87.5%) and Cochrane CENTRAL (n=110, 91.7%), and conducted independent and duplicate study selection (n=98, 81.7%), risk of bias assessment (n=105, 87.5%), and data collection (n=105, 87.5%). Only nine (7.5%) reviews clearly defined safety outcomes, and seven (5.8%) defined a primary safety outcome; none stated whether the primary safety outcome was pre-defined. Among the 80 reviews that pooled the primary dichotomous safety data across studies, less than half (41%; n=33) conducted subgroup analysis to explore for sources of heterogeneity or reported a GRADE assessment for the overall quality of evidence. Cochrane reviews were more likely to provide a study protocol (100% vs. 23.3%, P<0.001), involve methodologists (53.3% vs. 20.0%, P<0.001), and report a GRADE assessment for the primary safety outcome (70.6% vs. 19.6%, P<0.001).
CONCLUSIONS: Our findings highlighted areas for improved planning and analysis in the assessment of drug safety among systematic reviews. Cochrane reviews were superior to non-Cochrane reviews; however, most reviews did not pre-specify their safety outcomes or methods for analysis, explore sources of heterogeneity among pooled effects, or assess the overall quality of evidence with the GRADE approach.
PMID: 32247024 [PubMed – as supplied by publisher]
Source: ncbi 2
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