Performance of the Self-Controlled Case Series With Active Comparators for Drug Safety Signal Detection Using Merative MarketScan Research Databases.

IF 2.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Astrid Coste, Angel Y S Wong, Francois Haguinet, Andrew Bate, Ian J Douglas
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Abstract

Background: Despite testing of epidemiological methods in US Claims databases for signal detection, such data sources have not become a routine capability. 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.

Objectives: This study aims to evaluate the performance of the SCCS with and without active comparators for signal detection using US Merative MarketScan Commercial Claims and Medicare databases.

Methods: We applied the SCCS to macrolide and fluoroquinolone antibiotics, using amoxicillin and cefalexin as active comparators. In total, 7 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. A two-year observation period with a 30-day risk window after each dispensing was used. Diagnostic performance was measured using sensitivity and specificity with respect to the product labels.

Results: The SCCS without active comparators achieved sensitivities of 0.73 and 0.72 and specificities of 0.68 and 0.62 in commercial and Medicare claims, respectively, for pairs with sufficient power. Active comparators increased specificity up to 0.84 and 0.86, respectively, in Commercial Claims and Medicare but decreased sensitivity to 0.45 and 0.36.

Conclusions: MarketScan databases are potentially suitable for drug safety signal detection due to their large size and information contained. Using a carefully designed reference set of drug-outcome pairs well suited to the study design, the SCCS, while imperfect, performed comparably to optimal settings identified in previously published studies. Active comparators did not enhance overall performance but showed improved specificity by better controlling confounding by indication at the cost of reduced sensitivity.

Abstract Image

利用Merative MarketScan研究数据库进行药物安全信号检测的主动比较器自控案例系列的性能。
背景:尽管在美国索赔数据库中测试了流行病学方法用于信号检测,但此类数据源尚未成为常规能力。自我控制病例系列(SCCS)是使用真实世界数据进行药物安全信号检测的最有前途的方法之一,结合主动比较器可以通过解决适应症混淆问题来潜在地提高其性能。目的:本研究旨在利用US Merative MarketScan商业索赔和医疗保险数据库评估SCCS在信号检测方面的性能。方法:将SCCS应用于大环内酯类和氟喹诺酮类抗生素,以阿莫西林和头孢氨苄为活性比较物。总共从所有器官分类中选择了7种药物和30个结局。我们建立了104个阳性对照和58个阴性对照的参考集,使用分类框架确保所选药物结局对在理论上非常适合SCCS设计。2年观察期,每次配药后30天的风险窗口期。使用产品标签的敏感性和特异性来测量诊断性能。结果:无活性比较物的SCCS在商业和医疗保险索赔中,对于具有足够功率的配对,灵敏度分别为0.73和0.72,特异性分别为0.68和0.62。在商业索赔和医疗保险中,活性比较器的特异性分别增加到0.84和0.86,但敏感性降低到0.45和0.36。结论:MarketScan数据库容量大,信息量大,适合用于药物安全信号检测。SCCS使用精心设计的一组非常适合研究设计的药物结局对作为参考,虽然不完美,但其表现与先前发表的研究中确定的最佳设置相当。活性比较器没有提高总体性能,但通过降低灵敏度为代价的适应症更好地控制混杂,从而提高了特异性。
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来源期刊
CiteScore
4.80
自引率
7.70%
发文量
173
审稿时长
3 months
期刊介绍: The aim of Pharmacoepidemiology and Drug Safety is to provide an international forum for the communication and evaluation of data, methods and opinion in the discipline of pharmacoepidemiology. The Journal publishes peer-reviewed reports of original research, invited reviews and a variety of guest editorials and commentaries embracing scientific, medical, statistical, legal and economic aspects of pharmacoepidemiology and post-marketing surveillance of drug safety. Appropriate material in these categories may also be considered for publication as a Brief Report. Particular areas of interest include: design, analysis, results, and interpretation of studies looking at the benefit or safety of specific pharmaceuticals, biologics, or medical devices, including studies in pharmacovigilance, postmarketing surveillance, pharmacoeconomics, patient safety, molecular pharmacoepidemiology, or any other study within the broad field of pharmacoepidemiology; comparative effectiveness research relating to pharmaceuticals, biologics, and medical devices. Comparative effectiveness research is the generation and synthesis of evidence that compares the benefits and harms of alternative methods to prevent, diagnose, treat, and monitor a clinical condition, as these methods are truly used in the real world; methodologic contributions of relevance to pharmacoepidemiology, whether original contributions, reviews of existing methods, or tutorials for how to apply the methods of pharmacoepidemiology; assessments of harm versus benefit in drug therapy; patterns of drug utilization; relationships between pharmacoepidemiology and the formulation and interpretation of regulatory guidelines; evaluations of risk management plans and programmes relating to pharmaceuticals, biologics and medical devices.
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