A basic study design for expedited safety signal evaluation based on electronic healthcare data

Authors

  • Sebastian Schneeweiss MD, ScD

    Corresponding author
    1. Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital & Harvard Medical School, Boston, MA 02120, USA
    • Division of Pharmacoepidemiology and Pharmacoeconomics, 1620 Tremont Street, Suite 3030, Boston, MA 02120, USA.
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  • This manuscript was presented at a meeting convened by the Engelberg Center at The Brookings Institute, in collaboration with the Centers for Education and Research on Therapeutics (CERTs) on ‘Methods, Tools, and Scientific Operations for the Sentinel System’ chaired by Dr Rich Platt and Dr Mark McClellan, Washington, DC, 7 May 2010.

Abstract

Active drug safety monitoring based on longitudinal electronic healthcare databases (a Sentinel System), as outlined in recent FDA-commissioned reports, consists of several interlocked processes, including signal generation, signal strengthening, and signal evaluation. Once a signal of a potential drug safety issue is generated, signal strengthening and signal evaluation have to follow in short sequence in order to quickly provide as much information about the triggering drug-event association as possible.

This paper proposes a basic study design based on the incident user cohort design for expedited signal evaluation in longitudinal healthcare databases. It will not resolve all methodological issues nor will it fit all study questions arising within the framework of a Sentinel System. It should rather be seen as a guidance that will fit the majority of situations and serve as a starting point for adaptations to specific studies.

Such an approach will expedite and structure the process of study development and highlight specific assumptions, which is particularly valuable in a Sentinel System where signals are by definition preliminary and evaluation of signals is time critical. Copyright © 2010 John Wiley & Sons, Ltd.

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