Future risks of chronic kidney disease and end-stage kidney disease in infants with postnatally-repaired posterior urethral valve: A systematic review

S. Uwaezuoke, U. Muoneke, N. Mbanefo
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引用次数: 1

Abstract

Background and Objectives: Several studies show that most infants with posterior urethral valve (PUV) do not fully recover their renal function, despite postnatal interventions to obviate the consequences of lower urinary tract obstruction. This systematic review assesses the future risks of chronic kidney disease (CKD) and end-stage kidney disease (ESKD) in infants with postnatally-repaired PUV. Methods: We electronically searched PubMed, Medline, Embase, and Google Scholar databases for articles published between 2000 and 2020 (Date of the last search: September 12, 2020) using appropriate descriptors. We selected the studies based on adopted eligibility and exclusion criteria. We independently retrieved relevant data from the selected studies using a preconceived data-extraction form. We analyzed the aggregate data among the selected studies that signified future CKD and ESKD after the postnatal intervention and computed their mean prevalence rates. We also calculated the average point estimate of CKD and ESKD relative risks (RR) as the effect estimate at a 95% confidence interval. Results: Eleven studies were selected and reviewed, in which a total of 1362 patients were managed and followed up for variable periods. The aggregate data on ESKD prevalence from seven studies showed that a total of 112 patients developed ESKD out of a total patient-population of 446, giving a calculated mean ESKD prevalence of 24%. The CKD prevalence data in nine studies showed that 210 patients had CKD, out of 741 patients that were followed up, with a calculated mean CKD prevalence of 28%. The pooled RR of ESKD in seven studies and RR of CKD in nine studies was 0.5 (−0.48, 1.48) and 0.57 (−0.41, 1.55), respectively. Conclusions: Future risks of CKD and ESKD are still high in patients with postnatally-repaired PUV. We advocate a management approach that involves a synergy between pediatric nephrologists and urologists to ensure prompt renoprotective strategies and timely surgical intervention.
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先天性后尿道瓣膜修复的婴儿慢性肾病和终末期肾病的未来风险:一项系统综述
背景和目的:几项研究表明,大多数患有后尿道瓣膜(PUV)的婴儿,尽管产后干预以消除下尿路梗阻的后果,但仍不能完全恢复肾功能。本系统综述评估了先天性PUV修复后婴儿发生慢性肾脏疾病(CKD)和终末期肾脏疾病(ESKD)的未来风险。方法:我们以电子方式检索PubMed、Medline、Embase和Google Scholar数据库,检索2000年至2020年(最后一次检索日期:2020年9月12日)发表的文章。我们根据采用的资格和排除标准选择研究。我们使用预先设计的数据提取表格从选定的研究中独立检索相关数据。我们分析了所选研究中表明产后干预后未来CKD和ESKD的总数据,并计算了它们的平均患病率。我们还计算了CKD和ESKD相对风险(RR)的平均点估计值作为95%置信区间的效果估计值。结果:选择并回顾了11项研究,共管理1362例患者,并进行了不同时期的随访。来自7项研究的ESKD患病率汇总数据显示,在446名患者中,共有112名患者发生了ESKD,计算出ESKD的平均患病率为24%。九项研究的CKD患病率数据显示,在随访的741例患者中,210例患者患有CKD,计算出的平均CKD患病率为28%。7项研究中ESKD和9项研究中CKD的合并RR分别为0.5(- 0.48,1.48)和0.57(- 0.41,1.55)。结论:先天性PUV修复后发生CKD和ESKD的风险仍然很高。我们提倡一种管理方法,包括儿科肾病学家和泌尿科医生之间的协同作用,以确保及时的肾脏保护策略和及时的手术干预。
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