Pediatric to adult transition in chronic kidney disease: a scoping review.

IF 2.4 4区 医学 Q2 UROLOGY & NEPHROLOGY
Zachariah Alkhayri, Rama Safadi, Andrea Varghese, Mustafa Husein, Shay Tanna, Sahithi R Mallyala, Nikhil Rayarakula, Carol L Vincent, Rupesh Raina
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引用次数: 0

Abstract

Introduction: Chronic kidney disease (CKD) presents unique medical and psychosocial challenges in children and adolescents that differ from adult patients with CKD. Transitioning from pediatric to adult care is a critical period. Insufficient planning and inadequate preparation increase the risk of medication nonadherence, loss to follow-up, graft failure in transplant patients, and increased morbidity. Transition models address barriers to successful transition, yet vary in their approach.

Methods: We conducted a scoping review of the transition of care in pediatric CKD in accordance with PRISMA-ScR guidelines. We included PubMed/MEDLINE full-text articles, KDIGO guidelines, and grey literature on transition models between 1st January 2000 and 31st August 2025. Eligible studies included original research articles in English, human clinical trials, and guidelines specifically addressing pediatric-to-adult CKD transition of care.

Results: We identified barriers to effective transition at the patient, provider, and system levels. Patients often lacked health literacy, emotional readiness, or independence. Providers faced challenges with communication across pediatric and adult care teams. System-level obstacles included gaps in insurance coverage and limited resources. To assess readiness, models such as ON TRAC, TRAQ, RTQ, and the UNC TRxANSITION offer valuable questionnaires. Early preparation between the ages of 11-14, a gradual increase in patient autonomy, multidisciplinary teams' involvement, and structured transfer clinics are recommended for proper CKD transition.

Discussion: An effective transition is vital for improving both pediatric and adult health outcomes. Future research should focus on standardized protocols such as the Six Core Elements of Health Care Transition and the integration of technology-based tools to better engage adolescent patients. Structured and evidence-based transition models supported by healthcare systems can improve transition.

慢性肾脏疾病从儿童到成人的转变:一个范围综述。
慢性肾脏疾病(CKD)在儿童和青少年中表现出与成人CKD患者不同的独特的医学和社会心理挑战。从儿科到成人护理的过渡是一个关键时期。不充分的计划和准备增加了药物不依从、随访失败、移植患者移植失败和发病率增加的风险。转换模型处理成功转换的障碍,但方法不同。方法:我们根据PRISMA-ScR指南对儿童CKD的护理转变进行了范围审查。我们收录了PubMed/MEDLINE的全文文章、KDIGO指南和关于2000年1月1日至2025年8月31日过渡模型的灰色文献。符合条件的研究包括英文原创研究文章、人体临床试验和专门针对儿科到成人CKD护理过渡的指南。结果:我们确定了患者、提供者和系统层面有效过渡的障碍。患者通常缺乏健康知识、情绪准备或独立性。提供者面临着儿科和成人护理团队之间沟通的挑战。系统层面的障碍包括保险覆盖面的差距和有限的资源。为了评估准备情况,诸如ON TRAC、TRAQ、RTQ和UNC transition等模型提供了有价值的调查问卷。建议在11-14岁之间进行早期准备,逐渐增加患者的自主性,多学科团队的参与,以及结构化的转移诊所,以实现适当的CKD过渡。讨论:有效的过渡对于改善儿童和成人的健康结果至关重要。未来的研究应侧重于标准化方案,如卫生保健转型的六个核心要素和基于技术的工具的整合,以更好地吸引青少年患者。由卫生保健系统支持的结构化和循证过渡模型可以改善过渡。
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
BMC Nephrology
BMC Nephrology UROLOGY & NEPHROLOGY-
CiteScore
4.30
自引率
0.00%
发文量
375
审稿时长
3-8 weeks
期刊介绍: BMC Nephrology is an open access journal publishing original peer-reviewed research articles in all aspects of the prevention, diagnosis and management of kidney and associated disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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