Literature DB >> 27372236

Cervical repair of congenital tracheoesophageal fistula: Complications lurking!

Andrea Conforti1, Chiara Iacusso2, Laura Valfrè2, Marilena Trozzi3, Sergio Bottero3, Pietro Bagolan2.   

Abstract

AIM: Esophageal atresia (EA) and tracheoesophageal fistula (TEF) consist of a spectrum of rare congenital abnormalities. Although EA surgical treatment is well established, the outcome of EA with proximal fistula (type B and D EA) or isolated H-type fistula (type E EA) is poorly explored. These forms of EA shared a common surgical step: the need of a cervical approach to close the fistula. Therefore, the aim of present study is to evaluate postoperative outcomes of patients treated for Gross type B-D and E EA, on regards of their cervical surgery.
MATERIALS AND METHODS: A retrospective case series analysis of all patients affected by type B-D and E EA, and admitted to our tertiary care center between January 2003 and December 2014 was performed. All patients underwent preoperative flexible laryngo-tracheobronchoscopy (LTBS) as part of our standardized preoperative diagnostic assessment to define the diagnosis, evaluate preoperative vocal cord motility and to cannulate the fistula when required. Fistula closure was always performed through a right cervical access. Analysis of all cases and comparison between type B-D and E EA were performed. Mann-Whitney test, Chi-squared test and unpaired t test were used as appropriate; p<0.05 was considered significant.
RESULTS: During the study period, 180 EA newborns were treated. Proximal or isolated TEF was found in 18 patients (10%): 7 type B, 11 type E EA. Patients affected by type B and E EA/TEF frequently present associated major malformations (27%), and major cardiac abnormalities (44%). Major postoperative complications were: vocal cord paralysis (5 patients), bilateral in 2 infants requiring tracheostomy, cerebral ischemia (1 patient), and cardiac failure (1 patient).
CONCLUSION: Patients affected by type B and E EA have a high rate of associated abnormalities, and risk of possible sequelae. Postoperative complications are common, with possible transient vocal cord dismotility, but in some cases persistent paralysis may require tracheostomy. Therefore, both preoperative and postoperative LTBS is highly recommended to evaluate the presence of a proximal fistula, and vocal cord motility, even in asymptomatic patients, to rule out any possible intraoperative "surprise" and any vocal cord abnormality and to possibly define its pathogenesis (congenital vs. iatrogenic).
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Esophageal atresia; Isolated tracheoesophageal fistula; TEF

Mesh:

Year:  2016        PMID: 27372236     DOI: 10.1016/j.jpedsurg.2016.06.010

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  3 in total

1.  Long-term outcomes following H-type tracheoesophageal fistula repair in infants.

Authors:  Augusto Zani; Luai Jamal; Giovanni Cobellis; Justyna M Wolinska; Samuel Fung; Evan J Propst; Priscilla P L Chiu; Agostino Pierro
Journal:  Pediatr Surg Int       Date:  2016-11-28       Impact factor: 1.827

Review 2.  Respiratory Morbidity in Children with Repaired Congenital Esophageal Atresia with or without Tracheoesophageal Fistula.

Authors:  Maria Francesca Patria; Stefano Ghislanzoni; Francesco Macchini; Mara Lelii; Alessandro Mori; Ernesto Leva; Nicola Principi; Susanna Esposito
Journal:  Int J Environ Res Public Health       Date:  2017-09-27       Impact factor: 3.390

3.  Diagnostic and management strategies for congenital H-type tracheoesophageal fistula: a systematic review.

Authors:  Keerthika Sampat; Paul D Losty
Journal:  Pediatr Surg Int       Date:  2021-01-20       Impact factor: 1.827

  3 in total

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