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综述-先天性泌尿道疾病的肾移植。

Review - Renal transplantation for congenital urological diseases.

机构信息

Division of Urology, Department of Surgery, The Hospital for Sick Children, Toronto, Canada; Division of Urology, Department of Surgery, University of Toronto, Toronto, Canada.

Division of Urology, Department of Surgery, The Hospital for Sick Children, Toronto, Canada.

出版信息

J Pediatr Urol. 2024 Oct;20(5):990-997. doi: 10.1016/j.jpurol.2024.07.017. Epub 2024 Jul 24.

Abstract

INTRODUCTION

Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) are structural disorders originating prenatally and present at birth. Affecting 4.2 to 1000 per 10,000 births globally, CAKUT includes conditions like posterior urethral valves, cloacal anomalies, and reflux nephropathy. These anomalies can lead to chronic kidney disease (CKD) or end-stage kidney disease (ESKD) in children, necessitating renal replacement therapy or transplantation.

OBJECTIVES

This article aims to provide an updated perspective on pediatric kidney transplantation for children with CAKUT, emphasizing pre-transplant evaluation and management to optimize long-term outcomes.

METHODS

A comprehensive urologic evaluation is essential for children with ESKD being considered for kidney transplantation. Key pre-transplant investigations include kidney/bladder ultrasound (US), voiding cystourethrogram (VCUG), uroflowmetry, and urodynamics (UDS)/video-urodynamics (VUDS). Non-operative interventions such as pharmacotherapy and clean intermittent catheterization (CIC) are also considered. Surgical interventions, like augmentation cystoplasty or continent catheterizable channels, are evaluated based on individual patient needs.

RESULTS

Kidney/bladder US and VCUG provide essential anatomical information. UDS offers comprehensive functional data, identifying hostile bladders needing pre-transplant optimization. Non-surgical measures like anticholinergics and CIC improve bladder function, while surgical options enhance compliance and capacity. Concurrent interventions during transplantation are feasible but require careful consideration of risks and benefits.

DISCUSSION

Children with CAKUT undergoing kidney transplantation exhibit comparable or better graft survival rates than those without CAKUT. However, those with lower urinary tract obstructions (LUTO) may have poorer long-term outcomes. UDS is crucial for evaluating bladder function pre-transplant, guiding the need for interventions. Long-term monitoring for urinary tract infections (UTIs) and bladder dysfunction is essential.

CONCLUSION

Optimal outcomes in pediatric kidney transplantation for CAKUT patients require thorough pre-transplant evaluation and management, particularly for those with LUTO. Multidisciplinary approaches ensure careful monitoring and timely interventions, improving graft survival and quality of life for these patients.

摘要

引言

先天性肾和尿路畸形(CAKUT)是一种先天起源并在出生时即存在的结构异常。全球每 10000 名新生儿中就有 4.2 到 1000 名患有 CAKUT,包括后尿道瓣膜、泄殖腔畸形和反流性肾病等疾病。这些异常可能导致儿童慢性肾脏病(CKD)或终末期肾病(ESKD),需要进行肾脏替代治疗或移植。

目的

本文旨在为 CAKUT 患儿的儿科肾移植提供最新视角,强调移植前评估和管理,以优化长期结果。

方法

对于考虑进行肾移植的 ESKD 患儿,需要进行全面的泌尿科评估。关键的移植前检查包括肾脏/膀胱超声(US)、排尿性膀胱尿道造影(VCUG)、尿流率和尿动力学(UDS)/视频尿动力学(VUDS)。还考虑了非手术干预措施,如药物治疗和清洁间歇性导尿(CIC)。根据患者的个体需求,评估手术干预措施,如膀胱扩张术或 continent 可插管通道。

结果

肾脏/膀胱 US 和 VCUG 提供重要的解剖学信息。UDS 提供全面的功能数据,确定需要移植前优化的敌对膀胱。非手术措施,如抗胆碱能药物和 CIC,可改善膀胱功能,而手术选择可提高顺应性和容量。移植期间同时进行干预是可行的,但需要仔细考虑风险和收益。

讨论

接受肾移植的 CAKUT 患儿的移植物存活率与无 CAKUT 的患儿相当或更好。然而,有下尿路梗阻(LUTO)的患儿可能有较差的长期结果。UDS 对于移植前评估膀胱功能至关重要,指导干预的必要性。需要长期监测尿路感染(UTI)和膀胱功能障碍。

结论

CAKUT 患儿接受肾移植的最佳结果需要彻底的移植前评估和管理,特别是对于 LUTO 患儿。多学科方法确保了仔细的监测和及时的干预,提高了这些患者的移植物存活率和生活质量。

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