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AZDrugMiner: An Information Extraction System for Mining Patient-Reported Adverse Drug Events in Online Patient Forums

机译:AZDrugMiner:一种信息提取系统,用于在在线患者论坛中挖掘患者报告的不良药物事件

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Post-marketing drug surveillance is a critical component of drug safety. Drug regulatory agencies such as the U.S. Food and Drug Administration (FDA) rely on voluntary reports from health professionals and consumers contributed to its FDA Adverse Event Reporting System (FAERS) to identify adverse drug events (ADEs). However, it is widely known that FAERS underestimates the prevalence of certain adverse events. Popular patient social media sites such as DailyStrength and PatientsLikeMe provide new information sources from which patient-reported ADEs may be extracted. In this study, we propose an analytical framework for extracting patient-reported adverse drug events from online patient forums. We develop a novel approach - the AZDrugMiner system - based on statistical learning to extract ad-verse drug events in patient discussions and identify reports from patient experiences. We evaluate our system using a set of manually annotated forum posts which show promising performance. We also examine correlations and differences between patient ADE reports extracted by our system and reports from FAERS. We conclude that patient social media ADE reports can be extracted effectively using our proposed framework. Those patient reports can reflect unique perspectives in treatment and be used to improve patient care and drug safety.
机译:上市后药品监督是药品安全的重要组成部分。诸如美国食品和药物管理局(FDA)之类的药物监管机构依靠卫生专业人员和消费者的自愿报告,向其FDA不良事件报告系统(FAERS)做出贡献,以识别不良药物事件(ADE)。但是,众所周知,FAERS会低估某些不良事件的发生率。诸如DailyStrength和PatientLikeMe之类的受欢迎的患者社交媒体网站提供了新的信息来源,可以从中提取患者报告的ADE。在这项研究中,我们提出了一个分析框架,用于从在线患者论坛中提取患者报告的不良药物事件。我们基于统计学习,开发了一种新颖的方法-AZDrugMiner系统-在患者讨论中提取不良药物事件并从患者经验中识别报告。我们使用一组手动注释的论坛帖子评估我们的系统,这些帖子显示出令人鼓舞的性能。我们还将检查系统提取的患者ADE报告与FAERS报告之间的相关性和差异。我们得出结论,使用我们提出的框架可以有效地提取患者社交媒体ADE报告。这些患者报告可以反映出治疗的独特观点,并可以用于改善患者护理和药物安全性。

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