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Complications and follow-up of gastroschisis
Insights
This study reviewed 27 gastroschisis cases, noting improved surgical outcomes and reduced mortality. However, serious complications persist, especially with premature infants and associated anomalies.
Area of Science:
- Pediatric Surgery
- Neonatal Care
- Congenital Anomalies
Background:
- Gastroschisis is a congenital abdominal wall defect requiring surgical intervention.
- Historically, high mortality rates were associated with gastroschisis management.
- Improved neonatal care and surgical techniques have evolved over time.
Abstract:
Twenty-seven patients with gastroschisis were seen at the Red Cross War Memorial Children's Hospital between 1960 and 1977. Twenty-five children were operated on either by primary closure, by skin closure alone, or by the insertion of a reinforced Silastic pouch or patch. The mortality rate has been reduced from 62% to 33% over the past 6 years. Despite better metabolic and respiratory care and intravenous alimentation, serious complications still occur, particularly when prematurity and associated anomalies such as atresia or meconium ileus exist. Other problems were respiratory complications, ileus, perforation, gangrene, intestinal obstruction, enterocolitis and disaccharide intolerance. The long-term follow-up of some of these patients is described.
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