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Gastroschisis complicated by intestinal atresia
Journal of Pediatric Surgery
|June 1, 1981
Summary
Gastroschisis with intestinal discontinuity in infants can be successfully treated. Surgical repair of intestinal continuity, even after initial complications, leads to survival.
Area of Science:
- Pediatric Surgery
- Neonatal Care
- Gastrointestinal Surgery
Background:
- Gastroschisis is a congenital abdominal wall defect requiring surgical intervention.
- Associated intestinal injury, such as atresia or necrosis, complicates gastroschisis repair.
- Early management involves primary closure and decompression, with potential need for staged reconstruction.
Observation:
- Five infants with gastroschisis presented with loss of intestinal continuity within 4 years.
- These cases involved intestinal atresia or a gangrenous ileal segment.
- Initial management included gastroschisis closure, intestinal decompression, and either enterostomy or tube intubation.
Findings:
- Four infants underwent a second operation between 2 and 4 weeks of age to re-establish intestinal continuity.
- At reoperation, the previously matted intestine appeared normal with resolved edema and minimal adhesions.
- The initially perceived shortened intestine was found to be of adequate length for anastomosis.
Implications:
- Surgical repair of intestinal continuity in gastroschisis is feasible and successful.
- Accurate assessment of intestinal length is crucial and often underestimated at birth.
- Principles for repairing isolated neonatal intestinal atresia are applicable in these complex cases.