与护理网络分享患者技术偏好:利益相关者对痴呆症护理“Let’s Talk Tech”决策援助的看法。

IF 3.4 3区 医学 Q2 NEUROSCIENCES
Clara Berridge, Natalie R Turner, William B Lober, George Demiris, Jeffrey Kaye
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引用次数: 0

摘要

背景let 's Talk Tech (LTT)是一项针对失忆患者及其护理伙伴的自我管理的网络干预,旨在支持有关数字健康技术的决策。在过去的工作中,夫妻希望与他们更大的护理网络共享LTT偏好报告。目的:本研究旨在了解护理对想要与谁分享他们的技术偏好报告,为什么,如果和如何临床医生想要接收他们。方法15对轻度认知障碍(MCI)或早期痴呆患者(n = 15)和一名护理伴侣(n = 15)共同完成LTT和2个调查问题。护理合作伙伴完成了独立的随访访谈,来自4个阿尔茨海默病研究中心附属诊所的32名临床医生查看了LTT报告并完成了10个问题的调查。我们对调查结果使用描述性统计,对访谈使用专题分析。结果三分之二的护理伙伴(n = 10)希望与家庭成员分享报告。一半(n = 8)的人希望与临床医生分享,让他们了解二人组的计划,并促进有关技术选择的对话。32名临床医生中有30名表示,他们希望获得患者的技术偏好报告,25名希望通过电子健康记录(EHR)访问报告。结论:研究结果表明,共享技术偏好对家庭成员和医疗服务提供者都有潜在价值。临床医生高度接受在电子病历中访问技术偏好报告,并将技术讨论作为预先护理计划的一部分。未来的研究应该测试电子病历的整合和共享技术偏好的潜力,以支持以人为本的技术选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sharing patient technology preferences with care networks: Stakeholders' views of the "Let's Talk Tech" decision aid for dementia care.

BackgroundLet's Talk Tech (LTT) is a self-administered web intervention for people with memory loss and their care partners that supports decision-making about digital health technologies. In past work, dyads wanted to share LTT preference reports with their larger care networks.ObjectiveThis study aims to understand with whom care dyads want to share their technology preference reports and why, and if and how clinicians want to receive them.MethodsTogether, fifteen dyads of people living with mild cognitive impairment (MCI) or early-stage dementia (n = 15) and a care partner (n = 15) completed LTT and two survey questions. Care partners completed independent follow-up interviews, and 32 clinicians at four Alzheimer's Disease Research Center-affiliated clinics viewed an LTT report and completed a 10-question survey. We used descriptive statistics for survey responses and thematic analysis for interviews.ResultsTwo-thirds of care partners (n = 10) wanted to share the report with family members. Half (n = 8) wanted to share it with clinicians to keep them informed about the dyad's planning and facilitate conversations about technology options. 30 of 32 clinicians reported they would want their patients' technology preferences reports, with 25 wanting to access it via the electronic health record (EHR).ConclusionsFindings demonstrate potential value to both family dyads and providers of sharing technology preferences beyond the care dyad. Clinicians were highly receptive to accessing technology preference reports in EHRs and to having discussions about technology be a part of advance care planning. Future research should test integration in the EHR and the potential of sharing technology preferences to support person-centered technology choices.

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来源期刊
Journal of Alzheimer's Disease
Journal of Alzheimer's Disease 医学-神经科学
CiteScore
6.40
自引率
7.50%
发文量
1327
审稿时长
2 months
期刊介绍: The Journal of Alzheimer''s Disease (JAD) is an international multidisciplinary journal to facilitate progress in understanding the etiology, pathogenesis, epidemiology, genetics, behavior, treatment and psychology of Alzheimer''s disease. The journal publishes research reports, reviews, short communications, hypotheses, ethics reviews, book reviews, and letters-to-the-editor. The journal is dedicated to providing an open forum for original research that will expedite our fundamental understanding of Alzheimer''s disease.
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