Evidence map›Paper›PMID 41384613›Full record

ArticlePharmacoepidemiology and drug safety2025

Performance of the Self-Controlled Case Series With Active Comparators for Drug Safety Signal Detection Using the Clinical Practice Research Datalink (CPRD).

Astrid Coste, Angel Y S Wong, Francois Haguinet, Andrew Bate, Ian J Douglas

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Article in Pharmacoepidemiology and drug safety, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Astrid CosteLSHTM, Department of Non-Communicable Disease Epidemiology, London, UK.ORCID 0000-0003-4207-7447
Angel Y S WongLSHTM, Department of Non-Communicable Disease Epidemiology, London, UK.ORCID 0000-0002-8618-7333
Francois HaguinetGSK Global Safety, Wavre, Belgium.
Andrew BateLSHTM, Department of Non-Communicable Disease Epidemiology, London, UK.ORCID 0000-0003-3151-3653
Ian J DouglasLSHTM, Department of Non-Communicable Disease Epidemiology, London, UK.

Funding

GlaxoSmithKline
6 · The paper itself

Abstract

backgroundThere is little evidence about signal detection using UK primary care electronic health records (EHRs). The self controlled case series (SCCS) is one of the most promising methods for drug safety signal detection using real world data, and incorporating active comparators could potentially improve its performance by addressing confounding by indication.

objectivesThis study aims to evaluate the performance of the SCCS with and without active comparators for signal detection using the UK Clinical Practice Research Datalink (CPRD) Aurum.

methodsWe applied the SCCS to macrolide and fluoroquinolone antibiotics, using amoxicillin and cefalexin as active comparators. In total seven drugs, and 30 outcomes from all organ classes were selected. We developed a reference set of 104 positive controls and 58 negative controls, using a taxonomy framework to ensure the selected drug outcome pairs are theoretically well suited to the SCCS design. Two-year observation periods with a 30-day risk window after each dispensing were used. Diagnostic performance was measured using sensitivity and specificity with respect to the product labels.

resultsThe sensitivity and specificity of the SCCS without active comparator in the 2017/2018 observation period were 0.57 and 0.77 when limited to pairs with satisfactory power. Specificity increased up to 0.89 with active comparators, however sensitivity decreased to 0.18. Five drug-outcome pairs were signals of disproportionality before they were present on labels.

conclusionsUsing a carefully designed reference set of drug-outcome pairs well suited to the study design, the SCCS performed moderately well for signal detection in CPRD. Whilst active comparators effectively reduced confounding by indication, they also reduced the number of correctly identified positive controls, due to a reduction in power. We showed some evidence that SCCS is able to highlight SDRs before they were present on labels.

Indexed as

Adverse Drug Reaction Reporting SystemsAnti-Bacterial AgentsDatabases, FactualDrug-Related Side Effects and Adverse ReactionsElectronic Health RecordsAmoxicillinFluoroquinolonesHumansPrimary Health CareSensitivity and SpecificityUnited KingdomAmoxicillinAnti-Bacterial AgentsFluoroquinolonesClinical Practice Research Datalinkpharmacoepidemiologypharmacovigilancereal‐world dataself‐controlled case seriessignal detection

Identifiers

PMID41384613
PMCPMC12699507

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