Interview Results From a Telehealth Hospice Intervention for Children and Young Adults With Cancer.

IF 3.2 2区 医学 Q2 CLINICAL NEUROLOGY
Shaheen Rana, Nicholas P DeGroote, Ebonee Harris, Anna Lange, Karen Wasilewski-Masker, James L Klosky, Joanne Wolfe, Dio Kavalieratos, Katharine E Brock
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Abstract

Background and aims: Surveyed families of children and young adults with cancer who participated in a pilot study of three coordinated telehealth visits (triad of patient/family, hospital clinician, and hospice nurse) during the first month of hospice enrollment found telehealth feasible and were highly satisfied with hospice care. The aim of this study is to further explore adult patient and caregiver perspectives on telehealth, specifically the benefits of telehealth, trade-offs with in-person appointments, and the impact on patient care and family end-of-life preparations.

Methods: This is a single-arm prospective pilot study of patients aged 0-29-with cancer initiating hospice care between 2021 and 2022 and their caregivers. Semi-structured qualitative interviews were conducted with adult patients after the first telehealth visit and with caregivers during bereavement. Traditional content analysis methods were employed to analyze the interviews.

Results: The primary themes identified were (1) convenience and positive experiences with technology (addressing family questions and concerns, comfort of home, user-friendliness of technology), (2) benefits of coordinated appointments (improved collaboration/communication among team members and patient/caregiver understanding), (3) the positive impact of telehealth visits on care (symptom management, support, and preparation for end-of-life).

Conclusions: Adult patients enrolled in hospice and bereaved caregivers found coordinated telehealth visits to be beneficial, notably the convenience, comfort, time and cost savings of participating from home. Coordinated telehealth visits provide opportunities for hospice and hospital clinicians to communicate and collaborate on symptom management plans while supporting and guiding families in end-of-life preparations.

对患有癌症的儿童和青少年进行远程医疗临终关怀干预的访谈结果。
背景与目的:在接受安宁疗护登记的第一个月,参与三次协调远程医疗访视(病人/家属、医院临床医生和安宁疗护护士三方)的儿童和年轻癌症患者的家庭被调查发现,远程医疗是可行的,并且对安宁疗护非常满意。本研究的目的是进一步探讨成人患者和护理人员对远程医疗的看法,特别是远程医疗的好处,与面对面预约的权衡,以及对患者护理和家庭临终准备的影响。方法:这是一项单臂前瞻性试点研究,研究对象为年龄在0-29岁之间、在2021-2022年间开始安宁疗护的癌症患者及其照护者。在第一次远程医疗访问后与成年患者进行了半结构化定性访谈,并在丧亲期间与护理人员进行了访谈。采用传统的内容分析方法对访谈进行分析。结果:确定的主要主题是(1)便利和积极的技术体验(解决家庭问题和关注,家庭舒适,技术的用户友好性),(2)协调预约的好处(改善团队成员之间的协作/沟通和患者/护理人员的理解),(3)远程医疗访问对护理的积极影响(症状管理,支持和临终准备)。结论:参加安宁疗护的成年病人和丧亲照护者发现协调的远程医疗访视是有益的,特别是在家参与的便利性、舒适性、时间和成本节约。协调的远程保健访问为临终关怀和医院临床医生提供了就症状管理计划进行沟通和协作的机会,同时支持和指导家属进行临终准备。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.90
自引率
6.40%
发文量
821
审稿时长
26 days
期刊介绍: The Journal of Pain and Symptom Management is an internationally respected, peer-reviewed journal and serves an interdisciplinary audience of professionals by providing a forum for the publication of the latest clinical research and best practices related to the relief of illness burden among patients afflicted with serious or life-threatening illness.
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