Hsieh Miyuki Hsing-Chun, Liang Hsun-Yin, Tsai Chih-Ying, Tseng Yu-Ting, Chao Pi-Hui, Huang Wei-I, Chen Wen-Wen, Lin Swu-Jane, Lai Edward Chia-Cheng
Institute of Clinical Pharmacy and Pharmaceutical Sciences, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Taiwan Drug Relief Foundation (TDRF), Taipei, Taiwan.
Clin Epidemiol. 2023 Jan 18;15:91-107. doi: 10.2147/CLEP.S395922. eCollection 2023.
Development and evaluation of a drug-safety signal detection system integrating data-mining tools in longitudinal data is essential. This study aimed to construct a new triage system using longitudinal data for drug-safety signal detection, integrating data-mining tools, and evaluate adaptability of such system.
Based on relevant guidelines and structural frameworks in Taiwan's pharmacovigilance system, we constructed a triage system integrating sequence symmetry analysis (SSA) and tree-based scan statistics (TreeScan) as data-mining tools for detecting safety signals. We conducted an exploratory analysis utilizing Taiwan's National Health Insurance Database and selecting two drug classes (sodium-glucose co-transporter-2 inhibitors (SGLT2i) and non-fluorinated quinolones (NFQ)) as chronic and episodic treatment respectively, as examples to test feasibility of the system.
Under the proposed system, either cohort-based or self-controlled mining with SSA and TreeScan was selected, based on whether the screened drug had an appropriate comparator. All detected alerts were further classified as known adverse drug reactions (ADRs), events related to other causes or potential signals from the triage algorithm, building on existing drug labels and clinical judgement. Exploratory analysis revealed greater numbers of signals for NFQ with a relatively low proportion of known ADRs; most were related to indication, patient characteristics or bias. No safety signals were found. By contrast, most SGLT2i signals were known ADRs or events related to patient characteristics. Four were potential signals warranting further investigation.
The proposed system facilitated active and systematic screening to detect and classify potential safety signals. Countries with real-world longitudinal data could adopt it to streamline drug-safety surveillance.
开发并评估一种将数据挖掘工具集成到纵向数据中的药物安全信号检测系统至关重要。本研究旨在构建一种利用纵向数据进行药物安全信号检测的新分类系统,集成数据挖掘工具,并评估该系统的适用性。
基于台湾药物警戒系统的相关指南和结构框架,我们构建了一种分类系统,该系统集成了序列对称性分析(SSA)和基于树的扫描统计(TreeScan)作为检测安全信号的数据挖掘工具。我们利用台湾全民健康保险数据库进行了一项探索性分析,分别选择两类药物(钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)和非氟化喹诺酮类(NFQ))作为慢性治疗和发作性治疗的示例,以测试该系统的可行性。
在所提出的系统下,根据筛选出的药物是否有合适的对照,选择基于队列或自我对照的SSA和TreeScan挖掘方法。所有检测到的警报都根据现有药物标签和临床判断,进一步分类为已知的药物不良反应(ADR)、与其他原因相关的事件或分类算法产生的潜在信号。探索性分析显示,NFQ的信号数量较多,但已知ADR的比例相对较低;大多数与适应证、患者特征或偏倚有关。未发现安全信号。相比之下,大多数SGLT2i信号是已知的ADR或与患者特征相关的事件。有四个是值得进一步调查的潜在信号。
所提出的系统有助于进行主动和系统的筛选,以检测和分类潜在的安全信号。拥有真实世界纵向数据的国家可以采用该系统来简化药物安全监测。