Severe tracheomalacia associated with esophageal atresia: Results of surgical treatment

Robert M. Filler*, Antonio Messineo, Itzhak Vinograd

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

115 Scopus citations


This study reviews our experience from 1977 to 1991 with 32 children born with esophageal atresia and tracheoesophageal fistula (EA-TEF) who later underwent surgery for severe tracheomalacia. Indications for surgery included dying spells (21), inability to extubate the airway (nasotracheal tube 5, tracheotomy 3), and recurrent pneumonia (3). Diagnosis was confirmed by chest x-ray, esophagogram, and bronchoscopy. Aortopexy was performed in 31 of 32 children; a splint without aortopexy was used in one older girl. Splinting was also necessary in two of the 31 at the initial operation, when aortopexy failed to prevent tracheal collapse. There were four initial failures. Currently, 29 children are well (median follow-up, 6.6 years). Two have a tracheostomy in place, and one, who had a vascular ring divided after aortopexy, died at home of unknown cause 1 month later. These findings indicate that aortopexy provides long-term relief of severe symptoms of tracheomalacia associated with EA-TEF in almost all affected children. When aortopexy fails, the insertion of an airway splint may succeed; otherwise, tracheostomy is necessary.

Original languageEnglish
Pages (from-to)1136-1141
Number of pages6
JournalJournal of Pediatric Surgery
Issue number8
StatePublished - Aug 1992
Externally publishedYes


  • Tracheomalacia
  • aortopexy
  • esophageal atresia
  • tracheoesophageal malformation


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