在加拿大省级网络中整合慢性肾脏疾病护理的预先护理计划的推动因素和障碍。

IF 1.6 Q3 UROLOGY & NEPHROLOGY
Canadian Journal of Kidney Health and Disease Pub Date : 2025-07-01 eCollection Date: 2025-01-01 DOI:10.1177/20543581251350891
Helen H L Chiu, John Duncan, Sherri Lynn Kensall, Yanchini Rajmohan, Sushila Saunders, Sarah Thomas, Salma Wadhwania, Gaylene Hargrove
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引用次数: 0

摘要

背景:患有晚期慢性肾脏疾病的个体可以通过及时的提前护理计划和讨论他们的护理目标,从综合姑息治疗方法中获益。尽管文献和指南强调在慢性肾脏疾病管理中需要预先护理计划,但以治疗为中心的方法仍然是常态,部分原因是提供者不愿意参与预先护理计划对话。在不列颠哥伦比亚省(BC),启动了综合姑息肾病学(IPN)项目,以加强肾脏保健提供者对预先护理计划和护理目标讨论的参与,培训该省肾脏保健提供者发起严重疾病对话,并为全省肾脏网络的患者和提供者开发标准化资源。目的:作为质量改进的一部分,本研究强调了成人慢性肾病患者的卫生保健提供者参与预先护理计划的障碍/挑战和推动因素。设计:采用多方法研究。环境:加拿大不列颠哥伦比亚省。参与者:在非透析和透析护理机构工作的肾脏保健提供者。方法:通过半结构化调查、个人访谈和对全省慢性肾脏疾病患者的卫生保健提供者的焦点小组收集数据。结果:一项肾脏保健提供者调查(n = 90)的结果显示,自我报告的综合姑息治疗方法的知识以及参与预先护理计划讨论的能力和舒适度有所改善。一对一访谈(n = 15)和焦点小组访谈(n = 32)的结果表明,与患者采取关系方法,提高提供者对预先护理计划的舒适度和能力,明确谁应该参与预先护理计划对话的角色和责任,有利于患者护理。围绕推进综合姑息治疗方法的目标,支持护理团队之间的凝聚力,并为肾脏护理团队提供指导和有针对性的教育和资源,可以实现有效的预先护理计划讨论。局限性:本研究受限于有目的的抽样,样本量小,以及由于参与者兴趣和环境造成的潜在偏倚。结论:对于肾脏卫生保健提供者来说,有针对性的教育和资源,明确角色和责任,以及与患者的长期关系可能有助于推动文化转变,从以治疗为重点到在整个疾病过程中整合姑息治疗。试验注册:未注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enablers and Barriers to Integrating Advance Care Planning in Chronic Kidney Disease Care in a Canadian Provincial Network.

Background: Individuals with advanced chronic kidney disease benefit from an integrated palliative approach to care through timely advance care planning and discussions about their goals of care. Despite literature and guidelines emphasizing the need for advance care planning in chronic kidney disease management, treatment-focused approach remains the norm, partly due to provider reluctance and discomfort in engaging in advance care planning conversations. In British Columbia (BC), the Integrated Palliative Nephrology (IPN) project was launched to enhance kidney health care provider engagement in advance care planning and goals of care discussions, to train kidney health care providers in the province to initiate serious illness conversations, and to develop standardized resources for patients and providers across a provincial renal network.

Objective: As part of the quality improvement, this study highlights the barriers/challenges and enablers to engage in advance care planning for health care providers of adult patients with chronic kidney disease.

Design: A multi-methods approach was used.

Setting: British Columbia, Canada.

Participants: Kidney health care providers who worked in nondialysis and dialysis care settings.

Methods: Data were collected through semistructured surveys, individual interviews, and focus groups with health care providers across the province who care for patients with chronic kidney disease.

Results: The results of a kidney health care provider survey (n = 90) showed self-reported improvements in knowledge of the integrated palliative approach and competency and comfort engaging in advance care planning discussions. The results of one-on-one interviews (n = 15) and focus groups (n = 32) with kidney health care providers showed that taking a relational approach with patients, enhancing provider comfort and competency with advance care planning, clarifying roles and responsibilities around who should engage in advance care planning conversation was beneficial to patient care. Supporting cohesion among care teams around the goal of advancing an integrated palliative approach, and offering mentorship and targeted education and resources for the kidney care team, can enable effective advance care planning discussions.

Limitations: The study was limited by purposive sampling, a small sample size, and potential bias due to participant interests and settings.

Conclusions: For kidney health care providers, targeted education and resources, clarity around roles and responsibilities, and long-term relationships with patients may help advance the cultural shift from treatment focus to integrating palliative care across the continuum of the illness journey.

Trial registration: Not registered.

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来源期刊
CiteScore
3.00
自引率
5.90%
发文量
84
审稿时长
12 weeks
期刊介绍: Canadian Journal of Kidney Health and Disease, the official journal of the Canadian Society of Nephrology, is an open access, peer-reviewed online journal that encourages high quality submissions focused on clinical, translational and health services delivery research in the field of chronic kidney disease, dialysis, kidney transplantation and organ donation. Our mandate is to promote and advocate for kidney health as it impacts national and international communities. Basic science, translational studies and clinical studies will be peer reviewed and processed by an Editorial Board comprised of geographically diverse Canadian and international nephrologists, internists and allied health professionals; this Editorial Board is mandated to ensure highest quality publications.
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