[2024 EAU/ESPU pediatric urology guidelines: key updates and clinical interpretation of congenital lower urinary tract obstruction].

Q2 Medicine
Lingli Mei, Zhihui Zheng, Chang Tao, Guangjie Chen, Xiang Yan
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引用次数: 0

Abstract

Congenital lower urinary tract obstruction (CLUTO) is a spectrum of fetal malformations caused by anatomical abnormalities of the urethra, characterized by high rates of perinatal complications and mortality. The 2024 joint guideline from the European Association of Urology (EAU) and the European Society for Paediatric Urology (ESPU) introduces systematic revisions to the comprehensive management of CLUTO. Key updates encompass advancements in prenatal and postnatal screening and precise diagnosis, refined fetal prognosis assessment, clearer indications and modality selection for prenatal intervention, optimization of postnatal treatment strategies, and the establishment of a lifelong follow-up framework within an integrated care pathway. This article elucidates these key updates by comparing the 2024 EAU/ESPU guideline with the 2022 European Rare Kidney Disease Reference Network (ERKNet) Consensus. It also discusses ongoing controversies and future research directions. The aim is to provide clinicians with the latest evidence-based insights to inform practice, ultimately improving outcomes and quality of life for children with CLUTO.

[2024年EAU/ESPU儿科泌尿外科指南:先天性下尿路梗阻的关键更新和临床解释]。
先天性下尿路梗阻(CLUTO)是由尿道解剖异常引起的一系列胎儿畸形,其特点是围产期并发症和死亡率高。欧洲泌尿外科协会(EAU)和欧洲儿科泌尿外科学会(ESPU)的2024年联合指南对CLUTO的综合管理进行了系统修订。主要更新包括产前和产后筛查和精确诊断的进展,胎儿预后评估的改进,产前干预的适应症和模式选择的更明确,产后治疗策略的优化,以及在综合护理途径中建立终身随访框架。本文通过比较2024年EAU/ESPU指南与2022年欧洲罕见肾病参考网络(ERKNet)共识来阐明这些关键的更新。并讨论了目前存在的争议和未来的研究方向。目的是为临床医生提供最新的基于证据的见解,以告知实践,最终改善患有CLUTO的儿童的结果和生活质量。
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
3.80
自引率
0.00%
发文量
67
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