Pharmacogenomic augmented machine learning in electronic health record alerts: A health system-wide usability survey of clinicians

IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Caroline W. Grant, Jean Marrero-Polanco, Jeremiah B. Joyce, Barbara Barry, Ashley Stillwell, Kellie Kruger, Therese Anderson, Heather Talley, Mary Hedges, Jose Valery, Richard White, Richard R. Sharp, Paul E. Croarkin, Liselotte N. Dyrbye, William V. Bobo, Arjun P. Athreya
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引用次数: 0

Abstract

Pharmacogenomic (PGx) biomarkers integrated using machine learning can be embedded within the electronic health record (EHR) to provide clinicians with individualized predictions of drug treatment outcomes. Currently, however, drug alerts in the EHR are largely generic (not patient-specific) and contribute to increased clinician stress and burnout. Improving the usability of PGx alerts is an urgent need. Therefore, this work aimed to identify principles for optimal PGx alert design through a health-system-wide, mixed-methods study. Clinicians representing multiple practices and care settings (N = 1062) in urban, rural, and underserved regions were invited to complete an electronic survey comparing the usability of three drug alerts for citalopram, as a case study. Alert 1 contained a generic warning of pharmacogenomic effects on citalopram metabolism. Alerts 2 and 3 provided patient-specific predictions of citalopram efficacy with varying depth of information. Primary outcomes included the System's Usability Scale score (0–100 points) of each alert, the perceived impact of each alert on stress and decision-making, and clinicians' suggestions for alert improvement. Secondary outcomes included the assessment of alert preference by clinician age, practice type, and geographic setting. Qualitative information was captured to provide context to quantitative information. The final cohort comprised 305 geographically and clinically diverse clinicians. A simplified, individualized alert (Alert 2) was perceived as beneficial for decision-making and stress compared with a more detailed version (Alert 3) and the generic alert (Alert 1) regardless of age, practice type, or geographic setting. Findings emphasize the need for clinician-guided design of PGx alerts in the era of digital medicine.

电子健康记录警报中的药物基因组学增强型机器学习:针对临床医生的医疗系统可用性调查
利用机器学习整合的药物基因组(PGx)生物标志物可嵌入电子病历(EHR),为临床医生提供个性化的药物治疗结果预测。然而,目前电子病历中的药物警示大多是通用的(不是针对特定患者的),这会增加临床医生的压力和职业倦怠。提高 PGx 提示的可用性是当务之急。因此,这项工作旨在通过一项医疗系统范围内的混合方法研究,确定最佳 PGx 提示设计的原则。作为一项案例研究,我们邀请了代表城市、农村和医疗服务不足地区多种实践和医疗环境的临床医生(N = 1062)来完成一项电子调查,比较西酞普兰三种药物警示的可用性。警示 1 包含药物基因组学对西酞普兰代谢影响的通用警示。警报 2 和警报 3 提供了针对特定患者的西酞普兰疗效预测,信息深度各不相同。主要结果包括每个警报的系统易用性量表评分(0-100 分)、每个警报对压力和决策的感知影响以及临床医生对改进警报的建议。次要结果包括按临床医生的年龄、执业类型和地理环境对警报偏好的评估。采集的定性信息为定量信息提供了背景信息。最终的群组由 305 名不同地域和临床类型的临床医生组成。与更详细的版本(警报 3)和通用警报(警报 1)相比,简化的个性化警报(警报 2)被认为有利于决策和减轻压力,而与年龄、执业类型或地理环境无关。研究结果表明,在数字医学时代,临床医生需要在指导下设计 PGx 警报。
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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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