首页> 美国卫生研究院文献>Pharmaceutics >Subset Analysis for Screening Drug–Drug Interaction Signal Using Pharmacovigilance Database
【2h】

Subset Analysis for Screening Drug–Drug Interaction Signal Using Pharmacovigilance Database

机译:使用药物检测数据库筛选药物 - 药物相互作用信号的子集分析

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Many patients require multi-drug combinations, and adverse event profiles reflect not only the effects of individual drugs but also drug–drug interactions. Although there are several algorithms for detecting drug–drug interaction signals, a simple analysis model is required for early detection of adverse events. Recently, there have been reports of detecting signals of drug–drug interactions using subset analysis, but appropriate detection criterion may not have been used. In this study, we presented and verified an appropriate criterion. The data source used was the Japanese Adverse Drug Event Report (JADER) database; “hypothetical” true data were generated through a combination of signals detected by three detection algorithms. The accuracy of the signal detection of the analytic model under investigation was verified using indicators used in machine learning. The newly proposed subset analysis confirmed that the signal detection was improved, compared with signal detection in the previous subset analysis, on the basis of the indicators of (0.584 to 0.809), (= ; ) (0.302 to 0.596), (0.583 to 0.878), (0.170 to 0.465), - (0.399 to 0.592), and ( ) (0.821 to 0.874). The previous subset analysis detected many false drug–drug interaction signals. Although the newly proposed subset analysis provides slightly lower detection accuracy for drug–drug interaction signals compared to signals compared to the Ω shrinkage measure model, the criteria used in the newly subset analysis significantly reduced the amount of falsely detected signals found in the previous subset analysis.
机译:许多患者需要多药物组合,而不利的事件概况不仅反映了个别药物的影响,也反映了药物 - 药物相互作用。尽管有几种用于检测药物 - 药物相互作用信号的算法,但是早期检测不良事件需要简单的分析模型。最近,已经有报道了使用子集分析检测药物 - 药物相互作用的信号,但可能不使用适当的检测标准。在本研究中,我们提出并验证了适当的标准。使用的数据源是日本不利药物事件报告(JADER)数据库;通过三个检测算法检测到的信号的组合产生“假设”真实数据。使用机器学习中使用的指标验证了正在研究的分析模型的信号检测的准确性。新增的子集分析证实,在先前的子集分析中,基于(0.584至0.809)的指标(=;)(0.302至0.596)(0.583至0.878)(0.583至0.878)(0.583至0.878)(0.583至0.878)(0.583至0.878)(0.583至0.878)(0.583至0.878)(0.583至0.878)(0.583至0.878)进行改善),(0.170至0.465), - (0.399至0.592),和()(0.821至0.874)。先前的子集分析检测到许多错误的药物 - 药物相互作用信号。虽然与ω收缩测量模型相比,新增的子集分析为药物 - 药物交互信号的检测精度略低,但是新子集分析中使用的标准显着降低了先前子集分析中发现的错误检测信号的量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号