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Feeding troubles following delayed primary repair of esophageal atresia

S Cavallaro1, A Pineschi, G Freni

  • 1Department of Pediatric Surgery, Regina Margherita Children's Hospital, Torino, Italy.

Insights

Delayed primary anastomosis in esophageal atresia infants led to significant feeding difficulties and growth delays. These infants experienced more swallowing problems and respiratory issues compared to those with direct anastomosis.

Area of Science:

  • Pediatric Surgery
  • Gastroenterology
  • Developmental Biology

Background:

  • Long-gap esophageal atresia presents significant surgical challenges.
  • Delayed primary anastomosis is a surgical approach for specific esophageal atresia cases.
  • Esophageal motility disorders are common in congenital esophageal anomalies.

Purpose of the Study:

  • To compare feeding outcomes and growth in infants with long-gap esophageal atresia treated with delayed versus direct primary anastomosis.
  • To evaluate the impact of surgical timing on swallowing function, esophageal motility, and gastroesophageal reflux.
  • To identify long-term consequences of delayed anastomosis on infant development.

Main Methods:

  • Retrospective comparison of two groups of infants with long-gap esophageal atresia (delayed anastomosis, n=5; direct anastomosis, n=20).
  • Data collection via esophagrams, 24-hour pH monitoring, and questionnaires on growth and feeding.
  • Assessment of feeding patterns, growth parameters (height, weight), and clinical symptoms (dysphagia, vomiting, respiratory issues).

Main Results:

  • Infants in the delayed anastomosis group (Group B) showed significantly retarded bottle feeding, introduction of solids, height, and weight parameters.
  • Group B experienced more frequent feeding difficulties, dysphagia, vomiting, coughing, choking, and recurrent respiratory symptoms compared to Group A.
  • Esophageal motility was impaired in all patients, with more pooling, retrograde flow, and delayed clearing in Group B. Severe gastroesophageal reflux was noted in both groups, with delayed clearing times in refluxing children.

Conclusions:

  • Delayed primary anastomosis in long-gap esophageal atresia exacerbates congenital esophageal motility deficits.
  • This approach leads to protracted dysphagia, impacting infant feeding, growth, and overall well-being.
  • The findings highlight the significant challenges faced by families and healthcare providers managing these complex cases.

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