GRADE guidelines 17: assessing the risk of bias associated with missing participant outcome data in a body of evidence

dc.contributor.authorGordon, Guyatt H.
dc.contributor.authorEbrahim, Shanil
dc.contributor.authorAlonso-Coello, Pablo
dc.contributor.authorJohnston, Bradley C.
dc.contributor.authorMathioudakis, Alexander G.
dc.contributor.authorBriel, Matthias
dc.contributor.authorMustafa, Reem A.
dc.contributor.authorSun, Xin
dc.contributor.authorWalter, Stephen D.
dc.contributor.authorHeels-Ansdell, Diane M.
dc.contributor.authorNeumann, Ignacio
dc.contributor.authorKahale, Lara A.
dc.contributor.authorIorio, A. M.
dc.contributor.authorMeerpohl, Joerg J.
dc.contributor.authorSchunëmann, Holger J.
dc.contributor.authorAkl, Elie A.
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:49:59Z
dc.date.available2025-01-24T11:49:59Z
dc.date.issued2017
dc.description.abstractObjective To provide GRADE guidance for assessing risk of bias across an entire body of evidence consequent on missing data for systematic reviews of both binary and continuous outcomes. Study Design and Setting Systematic survey of published methodological research, iterative discussions, testing in systematic reviews, and feedback from the GRADE Working Group. Results Approaches begin with a primary meta-analysis using a complete case analysis followed by sensitivity meta-analyses imputing, in each study, data for those with missing data, and then pooling across studies. For binary outcomes, we suggest use of “plausible worst case” in which review authors assume that those with missing data in treatment arms have proportionally higher event rates than those followed successfully. For continuous outcomes, imputed mean values come from other studies within the systematic review and the standard deviation (SD) from the median SDs of the control arms of all studies. Conclusions If the results of the primary meta-analysis are robust to the most extreme assumptions viewed as plausible, one does not rate down certainty in the evidence for risk of bias due to missing participant outcome data. If the results prove not robust to plausible assumptions, one would rate down certainty in the evidence for risk of bias. © 2017 Elsevier Inc.
dc.identifier.doihttps://doi.org/10.1016/j.jclinepi.2017.05.005
dc.identifier.eid2-s2.0-85021808658
dc.identifier.pmid28529188
dc.identifier.urihttp://hdl.handle.net/10938/30922
dc.language.isoen
dc.publisherElsevier USA
dc.relation.ispartofJournal of Clinical Epidemiology
dc.sourceScopus
dc.subjectGrade
dc.subjectMissing participant data
dc.subjectRisk of bias
dc.subjectSystematic reviews
dc.subjectTrials
dc.subjectBias (epidemiology)
dc.subjectHumans
dc.subjectLost to follow-up
dc.subjectPatient dropouts
dc.subjectResearch design
dc.subjectReview literature as topic
dc.subjectRisk assessment
dc.subjectArticle
dc.subjectData analysis
dc.subjectIntention to treat analysis
dc.subjectOutcome assessment
dc.subjectPriority journal
dc.subjectStatistical bias
dc.subjectFollow up
dc.subjectHuman
dc.subjectLiterature
dc.subjectMethodology
dc.subjectPatient dropout
dc.subjectPractice guideline
dc.subjectStatistics and numerical data
dc.titleGRADE guidelines 17: assessing the risk of bias associated with missing participant outcome data in a body of evidence
dc.typeArticle

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