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Multiplicity of data in trial reports and the reliability of meta-analyses: empirical study

cris.virtualsource.author-orcidc0dd548b-3615-470c-8476-aa9a40d49236
cris.virtualsource.author-orcid27e66509-69e4-4bbf-ab62-ebd20b6d2e74
datacite.rightsopen.access
dc.contributor.authorNüesch, Eveline
dc.contributor.authorNüesch, Eveline
dc.contributor.authorHiggins, Julian P T
dc.contributor.authorJüni, Peter
dc.contributor.authorGøtzsche, Peter C
dc.date.accessioned2024-10-11T09:22:23Z
dc.date.available2024-10-11T09:22:23Z
dc.date.issued2011
dc.description.abstractObjectives To examine the extent of multiplicity of data in trial reports and to assess the impact of multiplicity on meta-analysis results. Design Empirical study on a cohort of Cochrane systematic reviews. Data sources All Cochrane systematic reviews published from issue 3 in 2006 to issue 2 in 2007 that presented a result as a standardised mean difference (SMD). We retrieved trial reports contributing to the first SMD result in each review, and downloaded review protocols. We used these SMDs to identify a specific outcome for each meta-analysis from its protocol. Review methods Reviews were eligible if SMD results were based on two to ten randomised trials and if protocols described the outcome. We excluded reviews if they only presented results of subgroup analyses. Based on review protocols and index outcomes, two observers independently extracted the data necessary to calculate SMDs from the original trial reports for any intervention group, time point, or outcome measure compatible with the protocol. From the extracted data, we used Monte Carlo simulations to calculate all possible SMDs for every meta-analysis. Results We identified 19 eligible meta-analyses (including 83 trials). Published review protocols often lacked information about which data to choose. Twenty-four (29%) trials reported data for multiple intervention groups, 30 (36%) reported data for multiple time points, and 29 (35%) reported the index outcome measured on multiple scales. In 18 meta-analyses, we found multiplicity of data in at least one trial report; the median difference between the smallest and largest SMD results within a meta-analysis was 0.40 standard deviation units (range 0.04 to 0.91). Conclusions Multiplicity of data can affect the findings of systematic reviews and meta-analyses. To reduce the risk of bias, reviews and meta-analyses should comply with prespecified protocols that clearly identify time points, intervention groups, and scales of interest.
dc.description.sponsorshipInstitut für Sozial- und Präventivmedizin (ISPM)
dc.identifier.doi10.7892/boris.7359
dc.identifier.isi000294599900001
dc.identifier.pmid21878462
dc.identifier.publisherDOI10.1136/bmj.d4829
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/77814
dc.language.isoen
dc.publisherBMJ Publishing Group
dc.publisher.placeLondon
dc.relation.ispartofBMJ
dc.relation.issn1756-1833
dc.relation.organizationInstitute of Social and Preventive Medicine
dc.titleMultiplicity of data in trial reports and the reliability of meta-analyses: empirical study
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issued4829
oaire.citation.startPaged4829
oaire.citation.volume343
oairecerif.author.affiliationInstitut für Sozial- und Präventivmedizin (ISPM)
oairecerif.author.affiliationInstitut für Sozial- und Präventivmedizin (ISPM)
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unibe.description.ispublishedpub
unibe.eprints.legacyId7359
unibe.journal.abbrevTitleBMJ
unibe.refereedtrue
unibe.subtype.articlejournal

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