A causal roadmap for generating high-quality real-world evidence

Author:

Dang Lauren E.ORCID,Gruber Susan,Lee Hana,Dahabreh Issa J.,Stuart Elizabeth A.,Williamson Brian D.ORCID,Wyss Richard,Díaz IvánORCID,Ghosh Debashis,Kıcıman Emre,Alemayehu Demissie,Hoffman Katherine L.,Vossen Carla Y.,Huml Raymond A.ORCID,Ravn Henrik,Kvist Kajsa,Pratley Richard,Shih Mei-Chiung,Pennello GeneORCID,Martin David,Waddy Salina P.,Barr Charles E.,Akacha Mouna,Buse John B.ORCID,van der Laan Mark,Petersen Maya

Abstract

Abstract Increasing emphasis on the use of real-world evidence (RWE) to support clinical policy and regulatory decision-making has led to a proliferation of guidance, advice, and frameworks from regulatory agencies, academia, professional societies, and industry. A broad spectrum of studies use real-world data (RWD) to produce RWE, ranging from randomized trials with outcomes assessed using RWD to fully observational studies. Yet, many proposals for generating RWE lack sufficient detail, and many analyses of RWD suffer from implausible assumptions, other methodological flaws, or inappropriate interpretations. The Causal Roadmap is an explicit, itemized, iterative process that guides investigators to prespecify study design and analysis plans; it addresses a wide range of guidance within a single framework. By supporting the transparent evaluation of causal assumptions and facilitating objective comparisons of design and analysis choices based on prespecified criteria, the Roadmap can help investigators to evaluate the quality of evidence that a given study is likely to produce, specify a study to generate high-quality RWE, and communicate effectively with regulatory agencies and other stakeholders. This paper aims to disseminate and extend the Causal Roadmap framework for use by clinical and translational researchers; three companion papers demonstrate applications of the Causal Roadmap for specific use cases.

Publisher

Cambridge University Press (CUP)

Subject

General Medicine

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