Diverticulum formation after circular myotomy for esophageal atresia
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Updated: Oct 29, 2026

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Published on: April 17, 2020
Insights
The Livaditis technique for esophageal atresia using circular myotomy can lead to complications like strictures or diverticula. Careful long-term follow-up is crucial for patients undergoing this procedure.
Area of Science:
- Pediatric Surgery
- Thoracic Surgery
- Congenital Abnormalities
Background:
- Esophageal atresia (EA) with tracheoesophageal fistula (TEF) is a complex congenital anomaly.
- Surgical correction often requires techniques to bridge the esophageal gap, especially in longer-gap EA.
Observation:
- This study reviewed six cases of EA treated with circular myotomy of the upper pouch (Livaditis technique) for end-to-end anastomosis.
- All six patients had a lower TEF and underwent surgery between 15 and 96 hours after birth without preoperative pouch elongation.
Findings:
- Three patients had uneventful outcomes, while three developed mild strictures responsive to dilatation.
- Two patients developed diverticula, one causing acute respiratory distress and the other severe dysphagia, necessitating esophageal replacement.
- Complications included ballooning at the myotomy site, strictures, and diverticula formation.
Implications:
- The Livaditis technique for EA requires vigilant early and late postoperative monitoring.
- Close surveillance is particularly important for patients with anastomotic strictures or associated tracheomalacia.
- Management of EA complications may involve dilatations or, in severe cases, esophageal replacement.
Abstract:
Out of our last 70 cases of esophageal atresia, a circular myotomy of the upper pouch (Livaditis technique) was required in six patients to achieve an end-to-end anastomosis: all had a lower tracheoesophageal fistula. They were operated on between 15 and 96 hours after birth, without any preoperative attempt of elongation of the upper pouch. Follow-up ranged from 14 to 77 months. Three patients had an uneventful postoperative course and late outcome, despite a moderate ballooning at the myotomy site in one. Three babies developed a mild stricture which responded easily to a few dilatations. Asymptomatic ballooning at the myotomy site was observed in one baby; the other two developed a diverticulum responsible for acute respiratory distress in one case and severe dysphagia in the other. both required esophageal replacement. These observations call attention to the fact that patients treated by myotomy should be followed very carefully early and late, especially if an anastomotic stricture develops or in case of associated tracheomalacia.
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