Comparative outcomes in intestinal atresia: a clinical outcome and pathophysiology analysis

Sathyaprasad Burjonrappa1, Elise Crete, Sarah Bouchard

  • 1Division of Pediatric Surgery, Department of Surgery, New York Medical College, Valhalla, New York, NY 10595, USA. sathyabc@yahoo.com

Insights

Outcomes for 130 intestinal atresias show distal types are hard to diagnose prenatally. Proximal atresias have lower birth weights, and screening for anomalies is crucial for all intestinal atresia cases.

Area of Science:

  • Pediatric Surgery
  • Gastroenterology
  • Neonatal Medicine

Background:

  • Intestinal atresia is a congenital condition requiring surgical intervention.
  • Understanding outcomes based on atresia location is vital for patient management.

Purpose of the Study:

  • To analyze the outcomes of 130 cases of intestinal atresia treated between 1982 and 2007.
  • To identify factors influencing diagnosis, treatment, and survival in different types of intestinal atresia.

Main Methods:

  • Retrospective analysis of patient records.
  • Data collected included atresia location, demographics, prenatal diagnosis rates, birth weight, associated anomalies, surgical procedures, time to oral feeds, re-interventions, and mortality.
  • Statistical analysis using Fisher test and ANOVA.

Main Results:

  • Duodenal atresia (DA) had lower birth weight (2,380.5g) compared to jejuno-ileal (JIA) and colonic atresia (CA).
  • Prenatal diagnosis rates varied: 46% for DA, 41% for JIA, and 12.5% for CA.
  • Mortality was zero for DA and CA, but six deaths occurred in the JIA group, often associated with severe anomalies or complications like sepsis.

Conclusions:

  • Distal intestinal atresias present diagnostic challenges antenatally.
  • Proximal atresias are associated with significantly lower birth weights.
  • Comprehensive screening for congenital anomalies is essential in all intestinal atresia patients.
Abstract

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