Abstract

ContextA 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. ObjectiveWe aim to provide clear recommendations for the initial clinical management and follow-up of children with a cSFK. Evidence acquisitionPubMed and EMBASE were searched to identify relevant publications, which were combined with guidelines on related topics and expert opinion. Evidence synthesisInitially, 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 cystourethrography 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. ConclusionsThis 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 summaryMany 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 long-term clinical aspects, which might need medical management.

Highlights

  • Every urologist takes care of patients with a solitary functioning kidney (SFK), and within the field of pediatric urology, for transition of care, and for adult urologists taking over the care of patients with a congenital anomaly, clear clinical management tools are needed

  • >5000 children are born with a congenital solitary functioning kidney (cSFK) in the USA and EU alone, and in most cases, a cSFK is the consequence of unilateral renal agenesis (URA) or multicystic dysplastic kidney (MCDK)

  • Patients with a cSFK could be considered as having an extra indication for a voiding cystourethrogram (VCUG) as high-grade vesicoureteral reflux (VUR) appears to be a risk factor for kidney scarring [23,24,25], and kidney scarring can be considered to pose an additional risk in patients with an already reduced kidney mass

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Summary

Introduction

Every urologist takes care of patients with a solitary functioning kidney (SFK), and within the field of pediatric urology, for transition of care, and for adult urologists taking over the care of patients with a congenital anomaly, clear clinical management tools are needed. This overview points to the urological and medical clinical aspects and provides long-term care guidance for children with a congenital solitary functioning kidney (cSFK), which is a developmental defect with an estimated prevalence of 1 in 1500 newborns [1,2,3]. When insufficient evidence was available, recommendations were formulated in consensus meetings among the authors

Pathophysiology
Clinical presentation
Assessment and diagnosis
Treatment and prognosis
18 URA 15 URA 22 URA 28 cSFK 49 SFK b 38 cSFK 50 cSFK 81 cSFK 301
Future perspectives
Findings
Conclusions
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