PROBAST: A tool to assess risk of bias and applicability of prediction model studies: Explanation and elaboration
Moons, Karel G.M.; Wolff, Robert F.; Riley, Richard D.; Whiting, Penny F.; Westwood, Marie; Collins, Gary S.; Reitsma, Johannes B.; Kleijnen, Jos; Mallett, Sue
(2019) Annals of Internal Medicine, volume 170, issue 1, pp. W1 - W33
(Article)
Abstract
Prediction models in health care use predictors to estimate for an individual the probability that a condition or disease is already present (diagnostic model) or will occur in the future (prognostic model). Publications on prediction models have become more common in recent years, and competing prediction models frequently exist for
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the same outcome or target population. Health care providers, guideline developers, and policymakers are often unsure which model to use or recommend, and in which persons or settings. Hence, systematic reviews of these studies are increasingly demanded, required, and performed. A key part of a systematic review of prediction models is examination of risk of bias and applicability to the intended population and setting. To help reviewers with this process, the authors developed PROBAST (Prediction model Risk Of Bias ASsessment Tool) for studies developing, validating, or updating (for example, extending) prediction models, both diagnostic and prognostic. PROBAST was developed through a consensus process involving a group of experts in the field. It includes 20 signaling questions across 4 domains (participants, predictors, outcome, and analysis). This explanation and elaboration document describes the rationale for including each domain and signaling question and guides researchers, reviewers, readers, and guideline developers in how to use them to assess risk of bias and applicability concerns. All concepts are illustrated with published examples across different topics. The latest version of the PROBAST checklist, accompanying documents, and filled-in examples can be downloaded from www.probast.org.
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Keywords: Internal Medicine
ISSN: 0003-4819
Publisher: American College of Physicians
Note: Funding Information: Disclosures: Dr. Wolff reports grants from Bayer, Biogen, Pfizer, UCB, Amgen, BioMarin, Grünenthal, Chiesi, and TESARO outside the submitted work. Dr. Westwood reports grants from Bayer, Biogen, Pfizer, UCB, Amgen, BioMarin, Grünenthal, Chiesi, and TESARO outside the submitted work. Dr. Kleijnen reports grants from Bayer, Biogen, Pfizer, UCB, Amgen, BioMarin, Grünenthal, Chiesi, and TESARO outside the submitted work. Authors not named here have disclosed no conflicts of interest. Disclosures can also be viewed at www.acponline.org/authors/icmje/ConflictOfInterestForms .do?msNum=M18-1376. Funding Information: Financial Support: Drs. Moons and Reitsma received financial support from the Netherlands Organisation for Scientific Research (ZONMW 918.10.615 and 91208004). Dr. Riley is a member of the Evidence Synthesis Working Group funded by the NIHR School for Primary Care Research (project 390). Dr. Whiting (time) was supported by the NIHR Collaboration for Leadership in Applied Health Research and Care West at University Hospitals Bristol NHS Foundation Trust. Dr. Collins was supported by the NIHR Biomedical Research Centre, Oxford. Dr. Mallett is supported by NIHR Birmingham Biomedical Research Centre at the University Hospitals Birmingham NHS Foundation Trust and the University of Birmingham. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Publisher Copyright: © 2019 American College of Physicians.
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