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青少年及家长代理在线记录访问:基于四项生物伦理原则的实证证据分析

Adolescent and parental proxy online record access: analysis of the empirical evidence based on four bioethical principles.

作者信息

Hagström Josefin, Hägglund Maria, Blease Charlotte

机构信息

Participatory eHealth and Health Data Research Group, Department of Women's and Children's Health, Uppsala University, Uppsala, Sweden.

MedTech Science & Innovation Centre, Uppsala University Hospital, Uppsala, Sweden.

出版信息

BMC Med Ethics. 2025 Feb 20;26(1):27. doi: 10.1186/s12910-025-01182-9.

Abstract

BACKGROUND

During recent decades, providing patients with access to their electronic health records (EHRs) has advanced in healthcare. In the European Union (EU), the General Data Protection Regulation provides individuals with the right to check their data in registries such as EHRs. A proposal for a European Health Data Space has been launched, which will further strengthen patients' right to have online access to their EHRs throughout Europe. Against these policy changes, scant attention has been paid to the ethical question about whether adolescents and parents should access the adolescent's EHR, and if so, under what conditions.

METHODS

In this paper, we apply biomedical ethical principles to explore key questions about adolescents' and parents' access to adolescents' EHRs, with the aim of informing future discussions about the development of ethical and policy practice guidelines.

RESULTS

Drawing on current empirical research, we find preliminary evidence that in some contexts, patient online record access (ORA) could help to facilitate autonomy for adolescents and parents as well as offering support in managing appointments and medications. Notably, however, we find contrasting perspectives between adolescents' and parents' experienced benefits and healthcare professionals' (HCPs) perceived potential harm, with the latter worried about decreased documentation quality after access. Concerns about capacity to understand their health information, and increased anxiety among adolescents obstruct the support of adolescent autonomy among parents and HCPs. Still, research is limited, particularly with respect to adolescents' experiences of reading their EHRs, and differences across settings have not been closely examined.

CONCLUSIONS

To advance more comprehensive understanding of the effects of ORA, and to inspire greater attention to, and development of, evidence-informed ethical guidance in this domain of clinical practice, we outline a range of empirical questions regarding adolescents' and parents' experiences that now warrant further study.

摘要

背景

在最近几十年里,让患者能够访问其电子健康记录(EHR)在医疗保健领域取得了进展。在欧盟(EU),《通用数据保护条例》赋予个人在诸如电子健康记录等登记处查看其数据的权利。一项关于欧洲健康数据空间的提案已经启动,这将进一步加强患者在整个欧洲在线访问其电子健康记录的权利。面对这些政策变化,对于青少年及其父母是否应该访问青少年的电子健康记录以及如果可以的话在何种条件下访问这一伦理问题,人们关注甚少。

方法

在本文中,我们应用生物医学伦理原则来探讨关于青少年及其父母访问青少年电子健康记录的关键问题,旨在为未来关于制定伦理和政策实践指南的讨论提供信息。

结果

借鉴当前的实证研究,我们发现初步证据表明,在某些情况下,患者在线记录访问(ORA)有助于促进青少年及其父母的自主性,同时在管理预约和用药方面提供支持。然而,值得注意的是,我们发现青少年和父母所体验到的益处与医疗保健专业人员(HCPs)所认为的潜在危害之间存在不同观点,后者担心访问后文档质量下降。对青少年理解其健康信息能力的担忧以及青少年焦虑情绪的增加阻碍了父母和医疗保健专业人员对青少年自主性的支持。尽管如此,研究仍然有限,特别是关于青少年阅读其电子健康记录的体验,而且不同环境下的差异尚未得到仔细研究。

结论

为了更全面地理解患者在线记录访问的影响,并激发对这一临床实践领域基于证据的伦理指导给予更多关注并加以发展,我们概述了一系列关于青少年及其父母体验的实证问题,这些问题现在值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/426d/11841295/83d65c30b24a/12910_2025_1182_Fig1_HTML.jpg

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