Literature DB >> 29327136

Signal Detection for Recently Approved Products: Adapting and Evaluating Self-Controlled Case Series Method Using a US Claims and UK Electronic Medical Records Database.

Xiaofeng Zhou1, Ian J Douglas2, Rongjun Shen3, Andrew Bate3,4.   

Abstract

INTRODUCTION: The Self-Controlled Case Series (SCCS) method has been widely used for hypothesis testing, but there is limited evidence of its performance for safety signal detection.
OBJECTIVE: The objective of this study was to evaluate SCCS for signal detection on recently approved products.
METHODS: A retrospective study covered the period after three recently marketed drugs were launched through to 31 December 2010 using The Health Improvement Network, a UK primary care database, and Optum, a US claims database. The SCCS method was applied to examine five heterogenous outcomes with desvenlafaxine and escitalopram and six outcomes with adalimumab for Signals of Disproportional Recording (SDRs); a positive finding was determined to be when the lower bound of 95% Confidence Interval of the incidence rate ratio (IRR) estimate was >  1. Multiple design choices were tested and the trend in IRR estimates over calendar time for one drug event pair was examined.
RESULTS: All six outcomes with adalimumab, three of five outcomes with desvenlafaxine, and four of five outcomes with escitalopram had SDRs. SCCS highlighted all acute events in the primary analysis but was less successful with slower-onset outcomes. Performance varied by risk period definition. Changes in IRR estimates over quarterly intervals for adalimumab with herpes zoster showed marked higher SDR within 9 months of drug launch.
CONCLUSION: SCCS shows promise for signal detection: it may highlight known associations for recent marketed products and has potential for early signal identification. SCCS performance varied by design choice and the nature of both exposure and event pair. Future work is needed to determine how effective the approach is in prospective testing and determining the performance characteristics of the approach.

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Mesh:

Year:  2018        PMID: 29327136     DOI: 10.1007/s40264-017-0626-y

Source DB:  PubMed          Journal:  Drug Saf        ISSN: 0114-5916            Impact factor:   5.606


  39 in total

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4.  Empirical performance of the self-controlled case series design: lessons for developing a risk identification and analysis system.

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Journal:  Drug Saf       Date:  2013-10       Impact factor: 5.606

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6.  Validation studies of the health improvement network (THIN) database for pharmacoepidemiology research.

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7.  Use of the self-controlled case series method in drug safety assessment.

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10.  The risk of fractures associated with thiazolidinediones: a self-controlled case-series study.

Authors:  Ian J Douglas; Stephen J Evans; Stuart Pocock; Liam Smeeth
Journal:  PLoS Med       Date:  2009-09-29       Impact factor: 11.069

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