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Clinical Management of Children with a Congenital Solitary Functioning Kidney: Overview and Recommendations
Sander Groen In 't Woud1,2, Rik Westland3, Wout F J Feitz4
1Department for Health Evidence, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, The Netherlands.
Insights
Children with a congenital solitary functioning kidney (cSFK) require lifelong monitoring for hypertension and chronic kidney disease (CKD). Early diagnosis and risk factor identification are crucial for managing cSFK and preventing kidney injury.
Area of Science:
- Pediatric Urology
- Nephrology
- Developmental Biology
Background:
- Congenital solitary functioning kidney (cSFK) is a common condition predisposing to hypertension and chronic kidney disease (CKD) due to hyperfiltration.
- Urologists frequently manage patients with cSFK, who may require lifelong care or present with later-life clinical issues.
- Understanding the long-term implications of cSFK is essential for pediatric and adult urological practice.
Purpose of the Study:
- To establish clear recommendations for the initial clinical management of children diagnosed with cSFK.
- To provide guidance on the appropriate follow-up protocols for pediatric patients with cSFK.
- To address the urological and medical aspects of long-term care for individuals with cSFK.
Main Methods:
- Systematic literature search of PubMed and EMBASE databases.
- Inclusion of relevant clinical guidelines and expert opinions to supplement search findings.
- Synthesis of evidence to formulate management and follow-up recommendations.
Main Results:
- Initial management involves confirming cSFK diagnosis and identifying kidney injury risk factors via ultrasound.
- Additional congenital anomalies and lack of compensatory hypertrophy are associated with poorer prognosis.
- Yearly follow-up for kidney injury signs, including annual ambulatory blood pressure monitoring, is recommended; ACE inhibitors are first-line for injury.
Conclusions:
- Children with cSFK are at lifelong risk of hypertension and CKD, necessitating continuous monitoring.
- Current evidence highlights the need for more large-scale, prospective studies for individualized risk-based management.
- Long-term urological and medical surveillance is critical for optimizing outcomes in patients with cSFK.
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 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.
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 long-term clinical aspects, which might need medical management.
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