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开发一种资源,供医疗专业人员在肾脏护理咨询期间提出预先护理计划主题:一种多用户中心设计。

Development of a Resource for Health Professionals to Raise Advance Care Planning Topics During Kidney Care Consultations: A Multiple User-Centered Design.

作者信息

Winterbottom Anna, Hurst Helen, Murtagh Fliss E M, Bekker Hilary L, Ormandy Paula, Hole Barnaby, Russon Lynne, Murphy Emma, Bucknall Keith, Mooney Andrew

机构信息

Leeds Renal Unit, Leeds Teaching Hospitals NHS Trust & Institute of Health Sciences, School of Medicine, University of Leeds, Leeds, UK.

School of Health and Society, University of Salford and Northern Care Alliance NHS Foundation Trust, Salford, UK.

出版信息

Kidney Med. 2024 Jul 18;6(9):100874. doi: 10.1016/j.xkme.2024.100874. eCollection 2024 Sep.

Abstract

RATIONALE & OBJECTIVE: Planning and delivering treatment pathways that integrate end-of-life care, frailty assessment, and enhanced supportive care is a service priority. Despite this, people with kidney failure are less likely to have an advance care plan and receive hospice and palliative care compared with other chronic illness populations. This is linked to health professionals feeling unskilled initiating conversations around future treatment and care options. This article describes research underpinning the development of a guide for kidney health professionals discussing end-of-life and advance care planning options with people with kidney failure and family members.

STUDY DESIGN

The study comprised 2 parts: an initial cross-sectional qualitative approach using in-depth interviews with older adults with kidney failure and (bereaved) carers followed by resource development with input from multiple stakeholders.

SETTING & PARTICIPANTS: Older adults with kidney failure and (bereaved) carers recruited from 2 renal units in the North of England and by online advertisements with national United Kingdom-based kidney patient charities. Resource development included input from co-applicants, independent advisory committee, patient and public involvement team, multidisciplinary health professionals and academics in the United Kingdom and Denmark.

ANALYTICAL APPROACH

Thematic analysis was used to analyze the data.

RESULTS

Twenty-seven people were interviewed: older adults with kidney failure (n = 18), carers (n = 5), bereaved carers (n = 4). Five themes are described: the context within which end-of-life conversations take place, preferences for end-of-life treatment and care, family members' role and needs in supporting people with kidney failure at the end-of-life, expectations and experience of dialysis treatment, and beliefs and experiences of death and dying.

LIMITATIONS

Participants were mainly White, British, and receiving hemodialysis.

CONCLUSIONS

People with (lived) experience of kidney failure informed a guide which aims to build on health professionals existing skills and improve confidence having conversations about future treatment and care. Kidney teams have expressed interest implementing the guide in practice and within their broader communications training packages.

摘要

原理与目的

规划并提供整合临终关怀、衰弱评估及强化支持性护理的治疗路径是一项服务重点。尽管如此,与其他慢性病群体相比,肾衰竭患者制定预先护理计划并接受临终关怀和姑息治疗的可能性较小。这与医疗专业人员在开启关于未来治疗和护理选择的对话时缺乏技能有关。本文描述了一项研究,该研究为肾脏健康专业人员制定了一份指南,用于与肾衰竭患者及其家属讨论临终关怀和预先护理计划选项。

研究设计

该研究包括两部分:最初采用横断面定性研究方法,对老年肾衰竭患者和(丧亲的)照料者进行深入访谈,随后在多个利益相关者的参与下进行资源开发。

研究背景与参与者

从英格兰北部的两个肾脏科病房招募老年肾衰竭患者和(丧亲的)照料者,并通过英国全国性肾脏患者慈善机构的在线广告进行招募。资源开发包括联合申请人、独立咨询委员会、患者及公众参与团队、英国和丹麦的多学科医疗专业人员及学者的参与。

分析方法

采用主题分析法对数据进行分析。

结果

共访谈了27人:老年肾衰竭患者(n = 18)、照料者(n = 5)、丧亲照料者(n = 4)。描述了五个主题:临终对话发生的背景、临终治疗和护理的偏好、家庭成员在临终时支持肾衰竭患者的角色和需求、透析治疗的期望和体验,以及对死亡和临终的信念和体验。

局限性

参与者主要是白人、英国人,且正在接受血液透析。

结论

有肾衰竭(生活)经历的人提供了一份指南,该指南旨在基于医疗专业人员现有的技能,增强他们就未来治疗和护理进行对话的信心。肾脏团队已表示有兴趣在实践中以及在更广泛的沟通培训包中实施该指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1431/11359737/f6b0c0838bad/gr1.jpg

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