Transitioning from CKD to Kidney Failure: A Mixed Methods Study of Patient Perspectives.

IF 8.2 1区 医学 Q1 UROLOGY & NEPHROLOGY
Megan Urbanski,Laura A Siminoff,Amy Waterman,Crystal A Gadegbeku,Levent Dumenci,Kimberly Jacob Arriola,Laura C Plantinga,Heather Gardiner
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Abstract

RATIONALE & OBJECTIVE The transition from chronic kidney disease (CKD) to kidney failure (KF) is life-changing. We explored the KF transition and dialysis start experiences of patients with varying degrees of prior nephrology care and preparation. STUDY DESIGN Convergent parallel mixed methods study using surveys and interviews. SETTING & PARTICIPANTS Data were collected from December 2018 to January 2020 among adults in metropolitan Philadelphia who had recently transitioned from CKD to KF and started dialysis. ANALYTICAL APPROACH Participants were categorized as either having had 1) some prior nephrology care and placement of an arteriovenous or peritoneal dialysis access, 2) minimal nephrology care (prior nephrology care, but no placement of a dialysis access), or 3) no prior nephrology care or placement of an access. Applied thematic analysis guided the qualitative analysis, and quantitative data were fully described. RESULTS KF transition was tumultuous for all participants (N=47), regardless of preparation (some prior care, n=23 [48.9%]; minimal prior care, n=13 [27.7%]; no prior care, n=11 [23.4%]). Dialysis start occurred along a spectrum of urgency with most (n=44; 93.6%) initiating dialysis in a hospital, and nearly all (n=46; 97.9%) were treated with in-center hemodialysis. Four additional themes emerged: (1) participants were unprepared to receive the KF diagnosis because they were unaware of the urgency of their medical situation; (2) the KF diagnosis communication environment was chaotic, but effective provider communication helped; (3) the first dialysis treatment was marked by intense apprehension and fear; and (4) participants prioritized making sense of their sudden new reality. LIMITATIONS Limited geographic representation and the exclusion of non-English-speaking participants. CONCLUSIONS Irrespective of prior preparation, participants experienced apprehension and fear during the transition from CKD to KF. Successfully addressing modifiable health system-level factors that affect this critical care transition and directly address the patient experience is needed to improve care and outcomes. PLAIN-LANGUAGE SUMMARY The progression from chronic kidney disease to kidney failure and dialysis is a challenging time for patients. We sought to understand the experiences of patients - those who had received prior kidney disease care, and those who had not - during this transition to kidney failure and dialysis treatment. We interviewed and surveyed 47 patients in metropolitan Philadelphia within 5 months of their dialysis initiation to understand and compare their experiences. Nearly all participants described this transition as traumatic and chaotic, even those with prior kidney disease care. This study underscores the need for patient-centered, health-system level programs that equip patients with the knowledge, resources, and support necessary to cope with this major life change and ultimately improve patient outcomes.
从CKD到肾衰竭的转变:一项混合方法的患者视角研究。
从慢性肾脏疾病(CKD)到肾衰竭(KF)的转变是改变生活的。我们探讨了不同程度的肾内科护理和准备的患者的KF转换和透析开始经验。研究设计使用调查和访谈的趋同平行混合方法研究。背景和参与者数据收集于2018年12月至2020年1月,来自费城大都会的成年人,他们最近从CKD过渡到KF并开始透析。分析方法:参与者被分类为:1)有一些先前的肾脏病学治疗并放置了动静脉或腹膜透析通道,2)最小的肾脏病学治疗(先前的肾脏病学治疗,但没有放置透析通道),或3)没有先前的肾脏病学治疗或放置了通道。应用专题分析指导定性分析,充分描述定量数据。结果所有参与者(N=47)的skf转换都是混乱的,无论是否做了准备(一些先前护理,N= 23[48.9%];最少的先前护理,N= 13[27.7%];没有先前护理,N= 11[23.4%])。透析开始是在紧急情况下发生的,大多数(n=44, 93.6%)在医院开始透析,几乎所有(n=46, 97.9%)患者都接受了中心血液透析治疗。出现了另外四个主题:(1)参与者没有准备好接受KF诊断,因为他们没有意识到自己医疗状况的紧迫性;(2) KF诊断沟通环境混乱,但有效的提供者沟通有所帮助;(3)第一次透析治疗表现出强烈的忧虑和恐惧;(4)参与者优先考虑如何理解他们突如其来的新现实。局限性:地域代表性有限,非英语国家的参与者被排除在外。结论:与之前的准备不同,参与者在从CKD到KF的转变过程中经历了忧虑和恐惧。要改善护理和结果,需要成功解决影响这一危重护理转变的可改变的卫生系统级因素,并直接解决患者体验。从慢性肾脏疾病发展到肾衰竭和透析对患者来说是一个具有挑战性的时期。我们试图了解患者的经历——那些之前接受过肾脏疾病治疗的患者和那些没有接受过肾脏疾病治疗的患者——在向肾衰竭和透析治疗过渡的过程中。我们在费城大都会对47名开始透析的患者进行了5个月内的访谈和调查,以了解和比较他们的经历。几乎所有的参与者都将这种转变描述为创伤性和混乱的,即使是那些先前有肾脏疾病治疗的人。本研究强调需要以患者为中心的卫生系统级项目,为患者提供应对这一重大生活变化所需的知识、资源和支持,并最终改善患者的预后。
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
American Journal of Kidney Diseases
American Journal of Kidney Diseases 医学-泌尿学与肾脏学
CiteScore
20.40
自引率
2.30%
发文量
732
审稿时长
3-8 weeks
期刊介绍: The American Journal of Kidney Diseases (AJKD), the National Kidney Foundation's official journal, is globally recognized for its leadership in clinical nephrology content. Monthly, AJKD publishes original investigations on kidney diseases, hypertension, dialysis therapies, and kidney transplantation. Rigorous peer-review, statistical scrutiny, and a structured format characterize the publication process. Each issue includes case reports unveiling new diseases and potential therapeutic strategies.
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