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.
Abstract

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