Preferred Reporting Items for a Systematic Review and Meta-analysis of Diagnostic Test Accuracy Studies

Matthew D. F. McInnes(University of Ottawa), David Moher(Ottawa Hospital), Brett D. Thombs(Jewish General Hospital), Trevor A. McGrath(University of Ottawa), Patrick M. Bossuyt(Amsterdam UMC Location University of Amsterdam), and the PRISMA-DTA Group(Canadian Agency for Drugs and Technologies in Health), Tammy Clifford(Délégation Paris 5), Jérémie F. Cohen(Délégation Paris 5), Jonathan J Deeks(Brown University), Constantine Gatsonis(Brown University), Lotty Hooft(University of Exeter), Harriet Hunt(University of Exeter), Christopher Hyde(University of Exeter), Daniël A. Korevaar(Amsterdam UMC Location University of Amsterdam), Mariska Leeflang(The University of Sydney), Petra Macaskill(The University of Sydney), Johannes B. Reitsma(Public Health Agency of Canada), Rachel Rodin(University of Bern), Anne WS Rutjes(University of Bern), Jean‐Paul Salameh(University of Ottawa), Adrienne Stevens(Ottawa Hospital), Yemisi Takwoingi(University of Calgary), Marcello Tonelli(Canadian Agency for Drugs and Technologies in Health), Laura Weeks(Canadian Agency for Drugs and Technologies in Health), Penny Whiting(National Institute for Health Research), Brian H Willis(University of Birmingham)
JAMA
January 23, 2018
Cited by 3,007Open Access
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Abstract

Importance: Systematic reviews of diagnostic test accuracy synthesize data from primary diagnostic studies that have evaluated the accuracy of 1 or more index tests against a reference standard, provide estimates of test performance, allow comparisons of the accuracy of different tests, and facilitate the identification of sources of variability in test accuracy. Objective: To develop the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) diagnostic test accuracy guideline as a stand-alone extension of the PRISMA statement. Modifications to the PRISMA statement reflect the specific requirements for reporting of systematic reviews and meta-analyses of diagnostic test accuracy studies and the abstracts for these reviews. Design: Established standards from the Enhancing the Quality and Transparency of Health Research (EQUATOR) Network were followed for the development of the guideline. The original PRISMA statement was used as a framework on which to modify and add items. A group of 24 multidisciplinary experts used a systematic review of articles on existing reporting guidelines and methods, a 3-round Delphi process, a consensus meeting, pilot testing, and iterative refinement to develop the PRISMA diagnostic test accuracy guideline. The final version of the PRISMA diagnostic test accuracy guideline checklist was approved by the group. Findings: The systematic review (produced 64 items) and the Delphi process (provided feedback on 7 proposed items; 1 item was later split into 2 items) identified 71 potentially relevant items for consideration. The Delphi process reduced these to 60 items that were discussed at the consensus meeting. Following the meeting, pilot testing and iterative feedback were used to generate the 27-item PRISMA diagnostic test accuracy checklist. To reflect specific or optimal contemporary systematic review methods for diagnostic test accuracy, 8 of the 27 original PRISMA items were left unchanged, 17 were modified, 2 were added, and 2 were omitted. Conclusions and Relevance: The 27-item PRISMA diagnostic test accuracy checklist provides specific guidance for reporting of systematic reviews. The PRISMA diagnostic test accuracy guideline can facilitate the transparent reporting of reviews, and may assist in the evaluation of validity and applicability, enhance replicability of reviews, and make the results from systematic reviews of diagnostic test accuracy studies more useful.


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