首页> 美国卫生研究院文献>Frontiers in Pharmacology >Can Electronic Health Records Databases Complement Spontaneous Reporting System Databases? A Historical-Reconstruction of the Association of Rofecoxib and Acute Myocardial Infarction
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Can Electronic Health Records Databases Complement Spontaneous Reporting System Databases? A Historical-Reconstruction of the Association of Rofecoxib and Acute Myocardial Infarction

机译:电子病历数据库可以补充自发报告系统数据库吗?罗非昔布与急性心肌梗死关联的历史重建

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摘要

Background: Several initiatives have assessed if mining electronic health records (EHRs) may accelerate the process of drug safety signal detection. In Europe, Exploring and Understanding Adverse Drug Reactions (EU-ADR) Project Focused on utilizing clinical data from EHRs of over 30 million patients from several European countries. Rofecoxib is a prescription COX-2 selective Non-Steroidal Anti-Inflammatory Drugs (NSAID) approved in 1999. In September 2004, the manufacturer withdrew rofecoxib from the market because of safety concerns. In this study, we investigated if the signal concerning rofecoxib and acute myocardial infarction (AMI) could have been identified in EHR database (EU-ADR project) earlier than spontaneous reporting system (SRS), and in advance of rofecoxib withdrawal.Methods: Data from the EU-ADR project and WHO-VigiBase (for SRS) were used for the analysis. Signals were identified when respective statistics exceeded defined thresholds. The SRS analyses was conducted two ways- based on the date the AMI events with rofecoxib as a suspect medication were entered into the database and also the date that the AMI event occurred with exposure to rofecoxib.Results: Within the databases participating in EU-ADR it was possible to identify a strong signal concerning rofecoxib and AMI since Q3 2000 [RR LGPS = 4.5 (95% CI: 2.84–6.72)] and peaked to 4.8 in Q4 2000. In WHO-VigiBase, for AMI term grouping, the EB05 threshold of 2 was crossed in the Q4 2004 (EB05 = 2.94). Since then, the EB05 value increased consistently and peaked in Q3 2006 (EB05 = 48.3) and then again in Q2 2008 (EB05 = 48.5). About 93% (2260 out of 2422) of AMIs reported in WHO-VigiBase database actually occurred prior to the product withdrawal, however, they were reported after the risk minimization/risk communication efforts.Conclusion: In this study, EU-EHR databases were able to detect the AMI signal 4 years prior to the SRS database. We believe that for events that are consistently documented in EHR databases, such as serious events or events requiring in-patient medical intervention or hospitalization, the signal detection exercise in EHR would be beneficial for newly introduced medicinal products on the market, in addition to the SRS data.
机译:背景:多项举措已经评估了挖掘电子健康记录(EHR)是否可以加速药物安全信号检测的过程。在欧洲,“探索和理解药物不良反应”(EU-ADR)项目的重点是利用来自欧洲多个国家的超过3000万患者的EHR的临床数据。罗非考昔是1999年批准的处方用COX-2选择性非甾体抗炎药(NSAID)。由于安全方面的考虑,制造商于2004年9月将罗非考昔从市场上撤回。在这项研究中,我们调查了在自发报告系统(SRS)之前和在罗非考昔撤药之前是否可以早于EHR数据库(EU-ADR项目)中识别出有关罗非昔布和急性心肌梗塞(AMI)的信号。方法:使用来自EU-ADR项目和WHO-VigiBase(用于SRS)的数据进行分析。当各个统计信息超出定义的阈值时,将识别信号。 SRS分析有两种方式-基于将以罗非考昔作为可疑药物的AMI事件输入数据库的日期,以及与罗非考昔接触的AMI事件发生的日期。结果:自2000年第3季度以来,参与EU-ADR的数据库就有可能识别出与rofecoxib和AMI有关的强信号[RR LGPS = 4.5(95%CI:2.84–6.72)],并在2000年第4季度达到峰值4.8。在WHO-VigiBase中,对于AMI术语分组,在2004年第四季度超过了EB05阈值2(EB05 = 2.94)。此后,EB05值一直持续上升,并在2006年第三季度达到峰值(EB05 = 48.3),然后在2008年第二季度再次达到峰值(EB05 = 48.5)。 WHO-VigiBase数据库中报告的AMI中约有93%(2422个中的2260个)实际发生在产品撤回之前,但是在最小化风险/风险沟通工作之后才报告了。结论:根据研究,EU-EHR数据库能够比SRS数据库提前4年检测到AMI信号。我们认为,对于EHR数据库中一致记录的事件(例如严重事件或需要住院医疗干预或住院的事件),EHR中的信号检测练习除了对市场上新推出的医药产品有利之外, SRS数据。

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