Congenital H-type tracheoesophageal fistula: A multicenter review of outcomes in a rare disease

J Pediatr Surg. 2017 Nov;52(11):1711-1714. doi: 10.1016/j.jpedsurg.2017.05.002. Epub 2017 May 11.

Abstract

Objective: To perform a multicenter review of outcomes in patients with H-type tracheoesophageal fistula (TEF) in order to better understand the incidence and causes of post-operative complications.

Background: H-type TEF without esophageal atresia (EA) is a rare anomaly with a fundamentally different management algorithm than the more common types of EA/TEF. Outcomes after surgical treatment of H-type TEF are largely unknown, but many authoritative textbooks describe a high incidence of respiratory complications.

Methods: A multicenter retrospective review of all H-type TEF patients treated at 14 tertiary children's hospital from 2002-2012 was performed. Data were systematically collected concerning associated anomalies, operative techniques, hospital course, and short and long-term outcomes. Descriptive analyses were performed.

Results: We identified 102 patients (median 9.5 per center, range 1-16) with H-type TEF. The overall survival was 97%. Most patients were repaired via the cervical approach (96%). The in-hospital complication rate, excluding vocal cord issues, was 16%; this included an 8% post-operative leak rate. Twenty-two percent failed initial extubation after repair. A total of 22% of the entire group had vocal cord abnormalities (paralysis or paresis) on laryngoscopy that were likely because of recurrent laryngeal nerve injury. Nine percent required a tracheostomy. Only 3% had a recurrent fistula, all of which were treated with reoperation.

Conclusions: There is a high rate of recurrent laryngeal nerve injury after H-type TEF repair. This underscores the need for meticulous surgical technique at the initial repair and suggests that early vocal cord evaluation should be performed for any post-operative respiratory difficulty. Routine evaluation of vocal cord function after H-type TEF repair should be considered.

The level of evidence rating: Level IV.

Keywords: Congenital esophageal anomaly; Neonatal; Pediatric; Recurrent laryngeal nerve injury; Tracheoesophageal fistula.

Publication types

  • Multicenter Study

MeSH terms

  • Child, Preschool
  • Esophagoplasty
  • Female
  • Humans
  • Incidence
  • Infant
  • Infant, Newborn
  • Laryngoscopy
  • Male
  • Postoperative Complications / epidemiology
  • Postoperative Complications / etiology
  • Rare Diseases
  • Recurrence
  • Recurrent Laryngeal Nerve Injuries / complications
  • Reoperation
  • Retrospective Studies
  • Tracheoesophageal Fistula / classification
  • Tracheoesophageal Fistula / surgery*
  • Tracheostomy