[Anorectal malformations: a 6-years review at the University Clinics of Lubumbashi]

Trésor Kibangula Kasanga1, Didier Tshibangu Mujinga1, Florent Tshibwid Zeng2

  • 1Département de Chirurgie, Faculté de Médecine, Cliniques Universitaires de Lubumbashi, Université de Lubumbashi, Lubumbashi, République Démocratique du Congo.

Insights

Anorectal malformations (ARM) are common in infants, often diagnosed late via intestinal obstruction. Early detection and consistent follow-up are crucial for improving outcomes and reducing mortality in these congenital anomalies.

Area of Science:

  • Pediatric Surgery
  • Congenital Anomalies
  • Neonatal Care

Background:

  • Anorectal malformations (ARM) encompass a spectrum of congenital anomalies affecting the genitourinary and anal structures.
  • Early diagnosis of ARM is critical for effective management and reducing associated mortality, particularly in resource-limited settings.

Observation:

  • A prospective study included 24 infants (median age 2 days) with ARM.
  • Intestinal obstruction was the most common diagnostic presentation (50%).
  • Low ARM, often without fistula, was frequent (45.7%), with intestinal atresia as the most common associated anomaly.

Findings:

  • Anoplasty was performed in 54.1% of patients.
  • Mortality was 25% (6/24), with 25% lost to follow-up.
  • Among reviewed patients, 75% (9/12) achieved fecal continence, predominantly those with low ARM.

Implications:

  • ARM diagnosis frequently occurs late, during intestinal obstruction, highlighting a need for improved early detection strategies.
  • High mortality and loss to follow-up underscore the necessity for enhanced long-term patient monitoring and care systems.
  • Strategies to improve early diagnosis and ensure consistent follow-up are vital for better functional outcomes and reduced mortality in ARM patients.

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