Clinical Management of Children with a Congenital Solitary Functioning Kidney: Overview and Recommendations

被引:37
作者
In't Woud, Sander Groen [1 ,2 ,5 ]
Westland, Rik [3 ]
Feitz, Wout F. J. [4 ]
Roeleveld, Nel [1 ]
van Wijk, Joanna A. E. [4 ]
van der Zanden, Loes F. M. [1 ]
Schreuder, Michiel F. [2 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Hlth Sci, Dept Hlth Evidence, Nijmegen, Netherlands
[2] Radboudumc Amalia Childrens Hosp, Radboud Inst Mol Life Sci, Dept Pediat Nephrol, Nijmegen, Netherlands
[3] Amsterdam UMC, Dept Pediat Nephrol, Amsterdam, Netherlands
[4] Radboudumc Amalia Childrens Hosp, Radboud Inst Mol Life Sci, Dept Urol, Div Pediat Urol, Nijmegen, Netherlands
[5] Radboud Univ Nijmegen, Med Ctr, Dept Hlth Evidence, POB 9101, NL-6500 HB Nijmegen, Netherlands
来源
EUROPEAN UROLOGY OPEN SCIENCE | 2021年 / 25卷
关键词
Clinical management; Congenital anomalies of the kidney and urinary tract; Multicystic dysplastic kidney; Solitary functioning kidney; Unilateral renal agenesis;
D O I
10.1016/j.euros.2021.01.003
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Context: A congenital solitary functioning kidney (cSFK) is a common developmental defect that predisposes to hypertension and chronic kidney disease (CKD) as a consequence of hyperfiltration. Every urologist takes care of patients with a cSFK, since some will need lifelong urological care or will come with clinical problems or questions to an adult urologist later in life. Objective: We aim to provide clear recommendations for the initial clinical management and follow-up of children with a cSFK. Evidence acquisition: PubMed and EMBASE were searched to identify relevant publications, which were combined with guidelines on related topics and expert opinion. Evidence synthesis: Initially, cSFK diagnosis should be confirmed and risk factors for kidney injury should be identified using ultrasound. Although more research into early predictors of kidney injury is needed, additional congenital anomalies of the kidney or urinary tract and absence of compensatory kidney hypertrophy have repeatedly been associated with a worse prognosis. The role of voiding cystour-ethrography and antibiotic prophylaxis remains controversial, and is complicated by the exclusion of children with a cSFK from studies. A yearly follow-up for signs of kidney injury is recommended for children with a cSFK. As masked hypertension is prevalent, annual ambulatory blood pressure measurement should be considered. During puberty, an increasing incidence of kidney injury is seen, indicating that long-term follow-up is necessary. If signs of kidney injury are present, angiotensin converting enzyme inhibitors are the first-line drugs of choice. Conclusions: This overview points to the urological and medical clinical aspects and long-term care guidance for children with a cSFK, who are at risk of hypertension and CKD. Monitoring for signs of kidney injury is therefore recommended throughout life. Large, prospective studies with long-term follow-up of clearly defined cohorts are still needed to facilitate more risk-based and individualized clinical management. Patient summary: Many children are born with only one functioning kidney, which could lead to kidney injury later in life. Therefore, a kidney ultrasound is made soon after birth, and other investigations may be needed as well. Urologists taking care of patients with a solitary functioning kidney should realize the longterm clinical aspects, which might need medical management. (C) 2021 The Author(s). Published by Elsevier B.V. on behalf of European Association of Urology.
引用
收藏
页码:11 / 20
页数:10
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