将电子健康记录用于临床药理学研究:挑战与考虑因素。

IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Eissa Jafari, Marisa H. Blackman, Jason H. Karnes, Sara L. Van Driest, Dana C. Crawford, Leena Choi, Caitrin W. McDonough
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引用次数: 0

摘要

电子健康记录(EHR)包含大量有关个人的表型数据,这些数据通常收集了数十年。由于信息量巨大,电子病历数据已成为我们在医疗保健系统中进行首次发现和识别差异的强大资源。近年来,基于电子病历的研究数量激增,但这些研究大多针对疾病相关因素,而非药物治疗结果,如药物反应或药物不良反应。这主要是由于从电子病历中得出药物相关表型所面临的挑战。在临床药理学研究中,基于电子病历的发现具有巨大潜力,而从电子病历中准确、可重复地得出药物相关表型的具体挑战亟待解决。本综述详细评估了从电子病历中获取药物相关数据的挑战和注意事项。我们对基于电子病历的可计算表型进行了研究,并讨论了为临床药理学研究绘制药物信息的前沿方法,包括基于药物的可计算表型和自然语言处理。我们还讨论了其他注意事项,如数据结构、异质性和缺失数据、罕见表型以及电子病历内的多样性。通过进一步了解与使用电子病历数据开展临床药理研究相关的复杂性,研究人员将能更好地设计深思熟虑的研究,使结果更具可重复性。在利用电子病历进行临床药理研究方面取得的进展应能大大提高我们了解不同药物反应和预测药物不良反应的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Using electronic health records for clinical pharmacology research: Challenges and considerations

Electronic health records (EHRs) contain a vast array of phenotypic data on large numbers of individuals, often collected over decades. Due to the wealth of information, EHR data have emerged as a powerful resource to make first discoveries and identify disparities in our healthcare system. While the number of EHR-based studies has exploded in recent years, most of these studies are directed at associations with disease rather than pharmacotherapeutic outcomes, such as drug response or adverse drug reactions. This is largely due to challenges specific to deriving drug-related phenotypes from the EHR. There is great potential for EHR-based discovery in clinical pharmacology research, and there is a critical need to address specific challenges related to accurate and reproducible derivation of drug-related phenotypes from the EHR. This review provides a detailed evaluation of challenges and considerations for deriving drug-related data from EHRs. We provide an examination of EHR-based computable phenotypes and discuss cutting-edge approaches to map medication information for clinical pharmacology research, including medication-based computable phenotypes and natural language processing. We also discuss additional considerations such as data structure, heterogeneity and missing data, rare phenotypes, and diversity within the EHR. By further understanding the complexities associated with conducting clinical pharmacology research using EHR-based data, investigators will be better equipped to design thoughtful studies with more reproducible results. Progress in utilizing EHRs for clinical pharmacology research should lead to significant advances in our ability to understand differential drug response and predict adverse drug reactions.

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来源期刊
Cts-Clinical and Translational Science
Cts-Clinical and Translational Science 医学-医学:研究与实验
CiteScore
6.70
自引率
2.60%
发文量
234
审稿时长
6-12 weeks
期刊介绍: Clinical and Translational Science (CTS), an official journal of the American Society for Clinical Pharmacology and Therapeutics, highlights original translational medicine research that helps bridge laboratory discoveries with the diagnosis and treatment of human disease. Translational medicine is a multi-faceted discipline with a focus on translational therapeutics. In a broad sense, translational medicine bridges across the discovery, development, regulation, and utilization spectrum. Research may appear as Full Articles, Brief Reports, Commentaries, Phase Forwards (clinical trials), Reviews, or Tutorials. CTS also includes invited didactic content that covers the connections between clinical pharmacology and translational medicine. Best-in-class methodologies and best practices are also welcomed as Tutorials. These additional features provide context for research articles and facilitate understanding for a wide array of individuals interested in clinical and translational science. CTS welcomes high quality, scientifically sound, original manuscripts focused on clinical pharmacology and translational science, including animal, in vitro, in silico, and clinical studies supporting the breadth of drug discovery, development, regulation and clinical use of both traditional drugs and innovative modalities.
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