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为改善肾衰竭患者临终关怀而开展的共享决策干预的可行性与可接受性:一项多中心随机对照试验试点研究

Feasibility and acceptability of the ShareD dEciSIon making for patients with kidney failuRE to improve end-of-life care intervention: A pilot multicentre randomised controlled trial.

作者信息

Buur Louise Engelbrecht, Bekker Hilary Louise, Søndergaard Henning, Kannegaard Michell, Madsen Jens Kristian, Khatir Dinah Sherzad, Finderup Jeanette

机构信息

Department of Renal Medicine, Aarhus University Hospital, Aarhus, Denmark.

Research Centre for Patient Involvement (ResCenPI), Aarhus University, Aarhus, Denmark.

出版信息

Int J Nurs Stud Adv. 2024 Aug 5;7:100231. doi: 10.1016/j.ijnsa.2024.100231. eCollection 2024 Dec.

Abstract

BACKGROUND

Kidney failure is associated with a high disease burden and high mortality rates. National and international guidelines recommend health professionals involve patients with kidney failure in making decisions about end-of-life care, but implementation of these conversations within kidney services varies. We developed the DESIRE (ShareD dEciSIon-making for patients with kidney failuRE to improve end-of-life care) intervention from our studies investigating multiple decision maker needs and experiences of end-of-life care in kidney services. The DESIRE intervention's three components are a training programme for health professionals, a patient decision aid, and a kidney service consultation held to facilitate shared decision-making conversations about planning end-of-life care.

OBJECTIVES

To assess the feasibility and acceptability of integrating the DESIRE intervention within kidney services.

DESIGN

A pilot study using a multicentre randomised controlled design.

SETTING

Four Danish nephrology departments.

PARTICIPANTS

Patients with kidney failure who were 75 years of age or above, their relatives, and health professionals.

METHODS

Patients were randomised to either the intervention or usual care. Feasibility data regarding delivering the intervention, the trial design, and outcome measures were collected through questionnaires and audio recordings at four points in time: before, during, post, and 3 months after the intervention. Acceptability data were collected through semi-structured interviews with patients and relatives, as well as a focus group with health professionals post the intervention.

RESULTS

Twenty-seven patients out of the 32 planned were randomised either to the intervention (= 14) or usual care (= 13). In addition, four relatives and 12 health professionals participated. Follow-up was completed by 81 % (= 22) of patient participants. We found that both feasibility and acceptability data suggested health professionals improved their decision support and shared decision-making skills via the training. Patient and relative participants experienced the intervention as supporting a shared decision-making process; from audio recordings, we showed health professionals were able to support proactively decision-making about end-of-life care within these consultations. All stakeholders perceived the intervention to be effective in promoting shared decision-making and relevant for supporting end-of-life care planning.

CONCLUSIONS

Participant feedback indicated that the DESIRE intervention can be integrated into practice to support patients, relatives, and health professionals in planning end-of-life care alongside the management of worsening kidney failure. Minimising exhaustion and enhancing engagement with the intervention should be a focus for subsequent refinement of the intervention.

REGISTRATION

The study has been registered at ClinicalTrials.gov with the identifier: NCT05842772. Date of first recruitment: March 20, 2023

摘要

背景

肾衰竭与高疾病负担和高死亡率相关。国家和国际指南建议医疗专业人员让肾衰竭患者参与临终关怀决策,但这些对话在肾脏服务中的实施情况各不相同。我们在研究中调查了肾脏服务中多个决策者对临终关怀的需求和经历,在此基础上开发了DESIRE(为改善肾衰竭患者临终关怀的共享决策)干预措施。DESIRE干预措施的三个组成部分是针对医疗专业人员的培训计划、患者决策辅助工具以及为促进关于临终关怀规划的共享决策对话而举行的肾脏服务咨询。

目的

评估将DESIRE干预措施整合到肾脏服务中的可行性和可接受性。

设计

采用多中心随机对照设计的试点研究。

地点

四个丹麦肾脏病科。

参与者

75岁及以上的肾衰竭患者、他们的亲属以及医疗专业人员。

方法

患者被随机分配到干预组或常规护理组。通过在四个时间点(干预前、干预期间、干预后和干预后3个月)进行问卷调查和录音,收集有关提供干预措施、试验设计和结果测量的可行性数据。通过对患者和亲属进行半结构化访谈以及在干预后与医疗专业人员进行焦点小组讨论来收集可接受性数据。

结果

计划中的32名患者中有27名被随机分配到干预组(=14)或常规护理组(=13)。此外,4名亲属和12名医疗专业人员参与了研究。81%(=22)的患者参与者完成了随访。我们发现,可行性和可接受性数据均表明,医疗专业人员通过培训提高了他们的决策支持和共享决策技能。患者和亲属参与者认为该干预措施有助于支持共享决策过程;从录音中可以看出,医疗专业人员能够在这些咨询中积极支持关于临终关怀的决策。所有利益相关者都认为该干预措施在促进共享决策方面有效,并且与支持临终关怀规划相关。

结论

参与者的反馈表明,DESIRE干预措施可以整合到实践中,以支持患者、亲属和医疗专业人员在管理肾衰竭恶化的同时规划临终关怀。尽量减少疲惫并增强对干预措施的参与度应是后续完善该干预措施的重点。

注册情况

该研究已在ClinicalTrials.gov注册,标识符为:NCT05842772。首次招募日期:2023年3月20日

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f11/11363568/e3fda090cd79/gr1.jpg

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