肾衰竭患者 "ShareD dEciSIon "改善临终关怀干预的可行性和可接受性:多中心随机对照试验

Louise Engelbrecht Buur , Hilary Louise Bekker , Henning Søndergaard , Michell Kannegaard , Jens Kristian Madsen , Dinah Sherzad Khatir , Jeanette Finderup
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引用次数: 0

摘要

背景肾衰竭与高疾病负担和高死亡率有关。国家和国际指南建议医护人员让肾衰竭患者参与生命末期护理决策,但在肾脏服务机构中,这些对话的实施情况各不相同。我们在调查肾脏服务中多个决策者的需求和临终关怀经验的基础上,开发了 DESIRE(肾衰竭患者分享决策以改善临终关怀)干预措施。目标评估将 DESIRE 干预纳入肾脏服务的可行性和可接受性。设计采用多中心随机对照设计进行试点研究。在干预前、干预中、干预后和干预后 3 个月的四个时间点,通过问卷和录音收集有关实施干预、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,以及在干预后与医护人员进行焦点小组讨论,收集了可接受性数据。结果在计划的 32 名患者中,有 27 名被随机分配到干预(14 人)或常规护理(13 人)中。此外,还有 4 名亲属和 12 名医疗专业人员参与。81%(22 人)的患者完成了随访。我们发现,可行性和可接受性数据都表明,医护人员通过培训提高了决策支持和共同决策技能。患者和亲属参与者认为干预措施支持了共同决策过程;通过录音,我们发现医护人员能够在这些咨询中积极主动地支持临终关怀决策。结论参与者的反馈意见表明,DESIRE 干预措施可与实践相结合,在治疗肾衰竭恶化的同时,支持患者、亲属和医疗专业人员规划临终关怀。最大限度地减少干预过程中的疲惫感和提高参与度应成为后续改进干预的重点。注册该研究已在ClinicalTrials.gov上注册,标识符为NCT05842772:NCT05842772。首次招募日期:2023 年 3 月 20 日:首次招募日期:2023 年 3 月 20 日。
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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

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 (n= 14) or usual care (n= 13). In addition, four relatives and 12 health professionals participated. Follow-up was completed by 81 % (n= 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.

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审稿时长
81 days
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