一种用于界定患者生成的健康数据临床责任的社会技术方法。
A sociotechnical approach to defining clinical responsibilities for patient-generated health data.
作者信息
Griffin Ashley C, Moyer Meagan F, Anoshiravani Arash, Hornsey Sondra, Sharp Christopher D
机构信息
Center for Biomedical Informatics Research, Stanford University School of Medicine, Stanford, CA, USA.
Center for Innovation to Implementation, VA Palo Alto Health Care System, Menlo Park, CA, USA.
出版信息
NPJ Digit Med. 2025 May 12;8(1):270. doi: 10.1038/s41746-025-01680-5.
The proliferation of health devices and apps has led to an abundance of patient-generated health data (PGHD), which has raised concerns about integration within clinical settings. We describe one health system’s sequential focus group approach for developing guiding principles to inform clinical responsibilities of PGHD. These principles center around (1) setting expectations; (2) preparing staffing and workflows; (3) delivering high-quality experiences; and (4) considerations for health information management of PGHD.
健康设备和应用程序的激增导致了大量患者生成的健康数据（PGHD），这引发了人们对其在临床环境中整合的担忧。我们描述了一个医疗系统采用的一系列焦点小组方法，以制定指导原则，为PGHD的临床职责提供信息。这些原则围绕以下几点：（1）设定期望；（2）准备人员配备和工作流程；（3）提供高质量体验；（4）PGHD健康信息管理的考量因素。
Zotero 插件