对远程自我管理帕金森病护理路径的可行性、可接受性和安全性进行真实世界评估:医疗保健改进计划。

IF 4 3区 医学 Q2 NEUROSCIENCES
Angie A Kehagia, Sarah Chowienczyk, Michelle Helena van Velthoven, Emma King, Tracie North, Deb Shenton, Jane Abraham, Joseph Langley, Rebecca Partridge, Ursula Ankeny, Terry Gorst, Emma Edwards, Sue Whipps, Martha Batup, Jane Rideout, Mat Swabey, Jemma Inches, Sue Bentley, Georgina Gilbert, Camille Carroll
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引用次数: 0

摘要

背景:帕金森病(PwP)患者对有效和高效护理的需求尚未得到满足。我们采取了一项服务改进措施,共同开发并实施了一种新的护理路径--居家护理(HBC),该护理路径基于支持性自我管理、远程监控以及在需要时触发医疗保健联系的能力:评估居家护理的可行性、可接受性和安全性:我们评估了首批 100 名接受居家护理的患者 6 个月的数据。患者监测在基线和 6 个月时进行,包括运动(MDS-UPDRS II 和加速度计)、非运动(NMSQ、PDSS-2、HADS)和生活质量(PDQ)测量。护理质量根据英国帕金森病国家审核标准进行审核。过程测量反映了可行性。采用问卷调查和半结构化访谈等混合方法评估可接受性:在 2019 年 10 月至 2021 年 1 月期间,108 名患者加入了 HBC,其中 100 名患者在 6 个月后获得了数据。所有调查问卷的回收率超过 90%,97% 的问卷内容完整或缺失项目小于 3 个。报告和沟通都在约定的时间内完成。与基线相比,在接受 HBC 治疗 6 个月后,帕金森病症状趋于稳定;更多的患者感到自己的意见被倾听(90% 对 79%),并且能够寻求帮助(79% 对 68%)。HBC 符合 93% 的国家审核标准。访谈的关键主题包括自主和赋权:我们已经证明了新型远程帕金森病护理路径的可接受性、可行性和安全性。确保可扩展性将扩大其覆盖范围,并为服务不足的社区带来益处,从而能够与标准护理和成本效益评估进行正式比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-World Evaluation of the Feasibility, Acceptability and Safety of a Remote, Self-Management Parkinson's Disease Care Pathway: A Healthcare Improvement Initiative.

Background: There is significant unmet need for effective and efficiently delivered care for people with Parkinson's disease (PwP). We undertook a service improvement initiative to co-develop and implement a new care pathway, Home Based Care (HBC), based on supported self-management, remote monitoring and the ability to trigger a healthcare contact when needed.

Objective: To evaluate feasibility, acceptability and safety of Home Based Care.

Methods: We evaluated data from the first 100 patients on HBC for 6 months. Patient monitoring, performed at baseline and 6-monthly, comprised motor (MDS-UPDRS II and accelerometer), non-motor (NMSQ, PDSS-2, HADS) and quality of life (PDQ) measures. Care quality was audited against Parkinson's UK national audit standards. Process measures captured feasibility. Acceptability was assessed using a mixed-methods approach comprising questionnaires and semi-structured interviews.

Results: Between October 2019 and January 2021, 108 PwP were enrolled onto HBC, with data from 100 being available at 6 months. Over 90% of all questionnaires were returned, 97% were complete or had < 3 missing items. Reporting and communications occurred within agreed timeframes. Compared with baseline, after 6m on HBC, PD symptoms were stable; more PwP felt listened to (90% vs. 79%) and able to seek help (79% vs. 68%). HBC met 93% of national audit criteria. Key themes from the interviews included autonomy and empowerment.

Conclusions: We have demonstrated acceptability, feasibility and safety of our novel remotely delivered Parkinson's care pathway. Ensuring scalability will widen its reach and realize its benefits for underserved communities, enabling formal comparisons with standard care and cost-effectiveness evaluation.

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来源期刊
CiteScore
8.40
自引率
5.80%
发文量
338
审稿时长
>12 weeks
期刊介绍: The Journal of Parkinson''s Disease (JPD) publishes original research in basic science, translational research and clinical medicine in Parkinson’s disease in cooperation with the Journal of Alzheimer''s Disease. It features a first class Editorial Board and provides rigorous peer review and rapid online publication.
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