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肾素 - 血管紧张素 - 醛固酮抑制剂治疗先天性肾脏和尿路异常儿童蛋白尿:尚需更多证据

Renin angiotensin aldosterone inhibitors in the treatment of proteinuria in children with congenital anomalies of the kidney and urinary tract: more evidence needed.

作者信息

Rivetti Giulio, Gizzone Pietro, Di Sessa Anna, Guarino Stefano, Miraglia Del Giudice Emanuele, Marzuillo Pierluigi

机构信息

Department of Woman, Child and of General and Specialized Surgery, Università degli Studi della Campania "Luigi Vanvitelli", Napoli, Italy.

出版信息

Expert Rev Clin Pharmacol. 2023 Jul-Dec;16(9):791-798. doi: 10.1080/17512433.2023.2247985. Epub 2023 Aug 20.

Abstract

INTRODUCTION

Congenital anomalies of the kidney and urinary tract (CAKUT) can be associated with proteinuria, possibly leading to a decline in kidney function. The aim of this review is to evaluate evidence on the efficacy of renin-angiotensin-aldosterone system inhibitors (RAASi) in children affected by CAKUT with proteinuria or chronic kidney disease (CKD).

AREAS COVERED

We conducted a bibliographic search between 1 December 2022 and 20 February 2023, including randomized controlled trials, case-control studies, observational studies, meta-analyses, and systematic reviews dealing with the efficacy of RAASi in reducing proteinuria and slowing the decline of kidney function in children.

EXPERT OPINION

RAASi are effective in reducing proteinuria and slowing CKD progression in many renal conditions; however, the efficacy of these drugs in patients affected by CAKUT with proteinuria is still unknown. While waiting for more evidence, when facing a child with CAKUT with isolated proteinuria or with proteinuria and CKD, a 6-12-month trial with RAASi with gradual increase to the maximal tolerated dose should be considered. If no improvement of proteinuria is obtained, the RAASi should be discontinued.

摘要

引言

先天性肾和尿路异常(CAKUT)可能与蛋白尿有关,这可能导致肾功能下降。本综述的目的是评估肾素-血管紧张素-醛固酮系统抑制剂(RAASi)对受CAKUT影响并伴有蛋白尿或慢性肾脏病(CKD)儿童的疗效证据。

涵盖领域

我们在2022年12月1日至2023年2月20日期间进行了文献检索,包括随机对照试验、病例对照研究、观察性研究、荟萃分析以及关于RAASi在降低儿童蛋白尿和减缓肾功能下降方面疗效的系统评价。

专家意见

RAASi在许多肾脏疾病中可有效降低蛋白尿并减缓CKD进展;然而,这些药物对受CAKUT影响并伴有蛋白尿患者的疗效仍不清楚。在等待更多证据时,当面对患有孤立性蛋白尿或伴有蛋白尿和CKD的CAKUT儿童时,应考虑进行为期6至12个月的RAASi试验,并逐渐增加至最大耐受剂量。如果蛋白尿没有改善,应停用RAASi。

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