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Impact of exposure accrual on sequential postmarket evaluations: a simulation study
Author(s) -
Maro Judith C.,
Brown Jeffrey S.
Publication year - 2011
Publication title -
pharmacoepidemiology and drug safety
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.023
H-Index - 96
eISSN - 1099-1557
pISSN - 1053-8569
DOI - 10.1002/pds.2223
Subject(s) - accrual , medicine , medicaid , food and drug administration , control (management) , environmental health , actuarial science , econometrics , accounting , computer science , business , health care , earnings , economics , economic growth , artificial intelligence
Purpose We frame the challenges in conducting sequential database surveillance (SDS) analyses and use simulation techniques to illustrate one of these aspects: the accrual of exposed person‐time. We discuss the role of SDS analyses in the US Food and Drug Administration's planned Sentinel System and suggest the outline of a decision–analytic framework that might aid regulatory authorities in planning postmarket surveillance. Methods We trace exposure accrual using US Medicaid data for new molecular entities approved in 2005 and 2006 and simulate risk estimates that are observable using SDS by varying the event rate of the health outcome of interest (HOI) in the control group. Results Sequential database surveillance may considerably narrow risk estimates for most products within 2 years when the underlying control group HOI occurs commonly ( i.e., at least 1 HOI/100 person‐years). Exposure accrual may be insufficient for detecting relative risks with infrequent, rare, or very rare HOIs (i.e., less frequent than 1 event/1000 person‐years). However, if SDS is used to quickly detect or rule out an incremental risk difference , then a majority of products are viable SDS candidates. Conclusions As a surveillance tool, SDS performs differently depending on whether its intended regulatory target is to narrow relative risk estimates or to confirm/rule out absolute levels of excess risk. These desired endpoints, in addition to the number of exposures available for analysis and the underlying HOI rates, influence the number of products that would be viable candidates for SDS. Copyright © 2011 John Wiley & Sons, Ltd.