GRADE guidelines: 18. How ROBINS-I and other tools to assess risk of bias in nonrandomized studies should be used to rate the certainty of a body of evidence

To provide guidance on how systematic review authors, guideline developers, and health technology assessment practitioners should approach the use of the risk of bias in nonrandomized studies of interventions (ROBINS-I) tool as a part of GRADE's certainty rating process. The study design and se...

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Veröffentlicht in:Journal of clinical epidemiology Jg. 111; S. 105 - 114
Hauptverfasser: Schünemann, Holger J., Cuello, Carlos, Akl, Elie A., Mustafa, Reem A., Meerpohl, Jörg J., Thayer, Kris, Morgan, Rebecca L., Gartlehner, Gerald, Kunz, Regina, Katikireddi, S Vittal, Sterne, Jonathan, Higgins, Julian PT, Guyatt, Gordon
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States Elsevier Inc 01.07.2019
Elsevier Limited
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ISSN:0895-4356, 1878-5921, 1878-5921
Online-Zugang:Volltext
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Zusammenfassung:To provide guidance on how systematic review authors, guideline developers, and health technology assessment practitioners should approach the use of the risk of bias in nonrandomized studies of interventions (ROBINS-I) tool as a part of GRADE's certainty rating process. The study design and setting comprised iterative discussions, testing in systematic reviews, and presentation at GRADE working group meetings with feedback from the GRADE working group. We describe where to start the initial assessment of a body of evidence with the use of ROBINS-I and where one would anticipate the final rating would end up. The GRADE accounted for issues that mitigate concerns about confounding and selection bias by introducing the upgrading domains: large effects, dose-effect relations, and when plausible residual confounders or other biases increase certainty. They will need to be considered in an assessment of a body of evidence when using ROBINS-I. The use of ROBINS-I in GRADE assessments may allow for a better comparison of evidence from randomized controlled trials (RCTs) and nonrandomized studies (NRSs) because they are placed on a common metric for risk of bias. Challenges remain, including appropriate presentation of evidence from RCTs and NRSs for decision-making and how to optimally integrate RCTs and NRSs in an evidence assessment.
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ISSN:0895-4356
1878-5921
1878-5921
DOI:10.1016/j.jclinepi.2018.01.012