青少年及其父母使用医院病人门户网站的伦理和法律考虑:医院伦理委员会成员的观点

Q1 Arts and Humanities
P. Sipanoun, J. Wray, K. Oulton, F. Gibson
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引用次数: 1

摘要

2019年4月,我们医院过渡到电子病历系统和患者门户(MyGOSH)。MyGOSH允许12岁或以上的年轻人及其父母访问结果、文件、预约,并与他们的护理团队沟通。进行焦点小组讨论,从医院伦理委员会成员的角度探讨青少年及其父母使用患者门户网站的伦理和法律考虑。招募了医院儿科生物伦理中心的成员(n = 7)。所有参与者均提供书面知情同意书。对焦点小组的讨论进行了记录、逐字抄录,并利用专题分析进行了分析。英国卫生研究机构研究伦理委员会(REC)由伦敦东南研究委员会批准(IRAS项目ID: 248793;参考文献:18/LO/1945)。确定了四个主题和子主题:(1)授予访问权限-评估能力/能力的复杂性,因未披露诊断而被排除在MyGOSH之外,以及说实话;(2)导致不平等的不平等——机会不平等的复杂性;(3)应对变化——提供支持和管理期望;(4)参与、授权和理解——数据安全,授权年轻人拥有自己的健康数据,一刀切的系统可能无法满足所有家庭的需求,以及与年轻人/父母的早期参与。让家庭访问门户网站可以提高参与度,使他们能够更多地参与护理工作,但也给所有人带来了挑战。复杂性存在于门户访问的评估,以及在提供公平服务的同时支持和管理用户期望。所有关注患者门户实施的利益相关者都需要持续的支持,以应对道德和法律的复杂性,并促进公平和门户实用程序,以造福患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The ethical and legal considerations of young people and their parents using a hospital patient portal: Hospital Ethics Committee members perspectives
In April 2019, our hospital transitioned to an electronic patient record system and patient portal (MyGOSH). MyGOSH enables young people aged 12 years or older and their parents to access results, documentation, appointments, and to communicate with their care team. A focus group was conducted to explore the ethical and legal considerations of young people and their parents using a patient portal from the perspective of hospital Ethics Committee members. Members of the hospital Paediatric Bioethics Centre were recruited ( n = 7). Written informed consent was provided by all participants. The focus group discussion was recorded, transcribed verbatim and analysed using thematic analysis. Health Research Authority Research Ethics Committee (REC) Approval was granted by London Southeast REC (IRAS Project ID: 248793; REC Reference: 18/LO/1945). Four themes, and sub-themes, were identified: (1) granting access – complexities of assessing competence/capacity, exclusion from MyGOSH due to non-disclosure of diagnosis, and truth-telling; (2) inequalities resulting in inequities – complexities of inequity in access; (3) responding to change – providing support and managing expectations; (4) engagement, empowerment and understanding – data safety, empowering young people to take ownership of their health data, a one-size fits all system may not meet the needs of all families, and early engagement with young people/parents. Giving families portal access can increase engagement, empowering them to be more involved in care, yet poses challenges for all. Complexities exist in the assessment for portal access, and supporting and managing user expectations whilst providing an equitable service. Ongoing support is required for all stakeholders following patient portal implementation to navigate the ethical and legal complexities, and to promote equity and portal utility for patient benefit.
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来源期刊
Clinical Ethics
Clinical Ethics Arts and Humanities-Philosophy
CiteScore
1.30
自引率
0.00%
发文量
42
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