"They Know You Better Than the Transplant Team": An Interpretive Description Study Exploring the Perspectives of Living Kidney Donors About Care Received From Family Physicians.

IF 1.5 Q3 UROLOGY & NEPHROLOGY
Canadian Journal of Kidney Health and Disease Pub Date : 2025-03-14 eCollection Date: 2025-01-01 DOI:10.1177/20543581251324548
Katya Loban, Charo Rodriguez, Antoine Przybylak-Brouillard, Elie Fadel, Heather Badenoch, Peter Nugus, Ann Bugeja, Justin Gill, Marie-Chantal Fortin, Emilie Trinh, Scott McKay, Shaifali Sandal
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引用次数: 0

Abstract

Background: Given the significant benefits of living donor kidney transplantation, the nephrology and transplant communities are augmenting efforts to increase living kidney donation. However, prior living kidney donors (LKDs) report suboptimal experiences and unmet care needs. The LKDs are healthy, and the vast majority have good outcomes post-donation. Thus, in clinical practice, their care is primarily assumed by practitioners, such as family physicians (FPs).

Objective: This study aimed to better understand the integration of primary care in LKDs' donation trajectory from the point of view of the latter. Our specific research questions were: (1) How do LKDs perceive the role of FPs currently integrated into the donation trajectory? (2) What are their needs and expectations from their FPs?

Design: An interpretive description methodology.

Setting and participants: Canadian LKDs who donated a kidney prior to 2020.

Methods: Qualitative interviews and inductive thematic analysis.

Results: In our sample of 49 LKDs who donated between 2007 and 2020, 61.2% were women and 87.8% were white. Also, 87.8% and 83.7% were attached to an FP pre- and post-donation (1 by a nurse practitioner) with 16.3% reporting no regular FP post-donation. Although participants provided varying accounts, an overwhelming majority described challenges with timely access to needed care; lack of cohesive continuity of care; variability in the services offered by FPs; and challenges with coordination of care between providers. Many reported poor coordination and communication between FPs and donor teams. Most articulated the desire to see an expanded role for FPs. This included improvements in knowledge regarding living donor care, information and care brokerage, continuous integrative care, and mental and emotional support.

Limitations: Limited transferability of our findings to other countries with variable payment structures.

Conclusions: Our work suggests that improving LKD care requires developing care pathways that facilitate donor transition and care coordination between donor teams and primary care practitioners. Given the challenges being faced by primary care in Canada, we believe that pragmatic strategies to better support primary care practitioners and a stronger integration of primary care with the living kidney donation process are essential. In addition, strategies to better support the mental health of LKDs are also needed. The LKDs provide a valuable gift to our health systems and to patients with kidney failure. It is our responsibility to optimize their experiences and improve their care.

“他们比移植团队更了解你”:一项探讨活体肾供者从家庭医生那里接受护理的观点的解释性描述研究。
背景:鉴于活体肾移植的显著好处,肾脏学和移植界正在加大努力,以增加活体肾捐赠。然而,先前的活体肾脏供者(LKDs)报告不理想的经历和未满足的护理需求。LKDs是健康的,绝大多数捐献后的结果都很好。因此,在临床实践中,他们的护理主要由从业者承担,如家庭医生(FPs)。目的:本研究旨在从低龄儿童捐献轨迹的角度,更好地了解初级保健在低龄儿童捐献轨迹中的整合。我们的具体研究问题是:(1)LKDs如何看待目前整合到捐赠轨迹中的FPs的作用?(2)他们对FPs的需求和期望是什么?设计:解释性描述方法。背景和参与者:在2020年之前捐赠肾脏的加拿大LKDs。方法:定性访谈和归纳专题分析。结果:在2007年至2020年期间捐赠的49名LKDs样本中,61.2%是女性,87.8%是白人。此外,87.8%和83.7%的人在捐献前和捐献后都有计划生育(1名护士执业),16.3%的人在捐献后没有定期计划生育。尽管参与者提供了不同的说法,但绝大多数人描述了及时获得所需护理的挑战;缺乏连贯的连续性;FPs所提供服务的可变性;以及提供者之间协调护理的挑战。许多国家报告说,FPs和捐助小组之间的协调和沟通很差。大多数人都希望看到FPs扮演更大的角色。这包括对活体捐赠者护理、信息和护理代理、持续综合护理以及精神和情感支持方面知识的改进。局限性:我们的研究结果在其他支付结构多变的国家的可转移性有限。结论:我们的工作表明,改善LKD护理需要发展护理途径,促进供体过渡和供体团队和初级保健从业人员之间的护理协调。考虑到加拿大初级保健面临的挑战,我们认为,更好地支持初级保健从业人员和加强初级保健与活体肾脏捐赠过程的整合的务实战略是必不可少的。此外,还需要制定战略,更好地支持弱势群体的心理健康。LKDs为我们的卫生系统和肾衰竭患者提供了一份宝贵的礼物。我们有责任优化他们的体验,改善他们的护理。
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
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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