Postoperative Genitourinary Challenges in Children with Anorectal Malformations: A Prospective Cohort Study

Fatemeh Abedi Karjiban1, Fariba Jahangiri2, Mahmoud Salek2

  • 1School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Insights

Anorectal malformations (ARM) are linked to neurogenic bladder and vesicoureteral reflux (VUR), particularly with posterior sagittal anorectoplasty (PSARP) and high-type ARM. Early diagnosis and follow-up are vital to prevent kidney failure.

Area of Science:

  • Pediatric Surgery
  • Urology
  • Congenital Anomalies

Background:

  • Anorectal malformations (ARM) are congenital defects often accompanied by genitourinary (GU) issues.
  • Surgical interventions for ARM include colostomy and posterior sagittal anorectoplasty (PSARP).

Purpose of the Study:

  • To assess the incidence of neurogenic bladder and vesicoureteral reflux (VUR) in pediatric patients with ARM.
  • To explore associations between these GU abnormalities and ARM type, fistula location, vertebral anomalies, and surgical techniques.

Main Methods:

  • A retrospective cohort study of 173 children with ARM was conducted over a 10-year period (July 2011-July 2021).
  • Genitourinary data, including urinary tract infections, VUR, and neurogenic bladder, were collected from medical records and follow-up visits.

Main Results:

  • Neurogenic bladder (37 patients) and VUR (44 patients) were diagnosed in a significant portion of the cohort.
  • Higher rates of neurogenic bladder and VUR were observed in patients undergoing PSARP.
  • Neurogenic bladder was more common in high-type ARM and rectourethral fistula cases, with recurrent UTIs highest in boys with high-type ARM.
  • Approximately 8% of patients developed signs of kidney failure.

Conclusions:

  • Genitourinary issues are common in ARM patients, necessitating parental education on regular follow-up.
  • Early detection and intervention are critical to prevent long-term kidney damage and progression to end-stage renal disease (ESRD).
Abstract

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