Diagnosis and Management of Congenital H-Type Tracheoesophageal Fistula: Results of a National Survey

Author:

Morchio Cecilia1,Ganarin Alba2,Conforti Andrea3,Leva Ernesto4,Gaglione Giovanni5,Brenco Gaia6,Zambaiti Elisa7ORCID,Chiarenza Salvatore Fabio8,Caldaro Tamara9,Cheli Maurizio10,Boroni Giovanni11ORCID,Marcandella Elena Sofia12ORCID,Riccipetitoni Giovanna1314,Cacciaguerra Sebastiano15,Di Benedetto Vincenzo16,Gentilino Valerio17,Lisi Gabriele18ORCID,Morini Francesco19,Midrio Paola2

Affiliation:

1. School of Pediatric Surgery, University of Florence, 50100 Florence, Italy

2. Pediatric Surgery Unit, Ca’ Foncello Hospital, 31100 Treviso, Italy

3. Neonatal Surgery Unit, Medical and Surgical Department of Fetus-Newborn-Infant, Bambino Gesù Children’s Hospital, IRCCS, 00100 Rome, Italy

4. Pediatric Surgery Unit, Fondazione IRCCS Ca’ Granda—Ospedale Maggiore Policlinico, University of Milan, 20100 Milan, Italy

5. UOC Pediatric Surgery Unit, AORN Santobono-Pausilipon, 80100 Naples, Italy

6. Pediatric Surgery Unit, IRCCS Giannina Gaslini’s Hospital, 16100 Genova, Italy

7. Department of Pediatric General Surgery, Regina Margherita Children’s Hospital, Azienda Ospedaliero Universitaria Città della Salute e della Scienza, 10100 Turin, Italy

8. Department of Pediatric Surgery, San Bortolo Hospital, 36100 Vicenza, Italy

9. Digestive Endoscopy and Surgery Unit, Bambino Gesu Children’s Hospital, IRCCS, 00100 Rome, Italy

10. Pediatric Surgery Unit, Ospedale Papa Giovanni XXIII, 24100 Bergamo, Italy

11. Department of Paediatric Surgery, ASST Spedali Civili di Brescia, 25100 Brescia, Italy

12. Paediatric Surgery Unit, Women’s and Children’s Health Department, University of Padua, 35100 Padua, Italy

13. Department of Paediatric Surgery, “V. Buzzi” Children’s Hospital, 20100 Milan, Italy

14. Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, Fondazione IRCCS Policlinico San Matteo, 27100 Pavia, Italy

15. Department of Pediatric Surgery, Ospedale Garibaldi-Nesima, 95100 Catania, Italy

16. Department of Pediatric Surgery, G. Rodolico—San Marco Hospital, 95100 Catania, Italy

17. Division of Pediatric Surgery, Woman and Child Department, “Filippo Del Ponte” Hospital, ASST Sette Laghi, 21100 Varese, Italy

18. Pediatric Surgery Unit, Santo Spirito Hospital, University of Chieti-Pescara, 65100 Pescara, Italy

19. Department of Maternal and Child Health and Urological Sciences, La Sapienza University, 00100 Rome, Italy

Abstract

Background: Congenital h-type tracheoesophageal fistula (H-TEF) without esophageal atresia (EA) represents about 4% of congenital esophageal anomalies. The diagnosis is challenging, and surgery is considered curative. The aim was to report a national survey on the diagnosis, management, and outcome of patients with congenital H-TEF. Methods: Following approval of the Italian Society of Pediatric Surgery, a survey was sent to all Pediatric Surgery Units to retrospectively collect H-TEF treated in the period 2010–2022. Descriptive analysis was performed, and results are given as prevalence, mean ± standard deviation (SD), or median and interquartile range (IQR). Results: The survey was sent to 65 units. Seventeen responded with one or more cases; 78 patients were diagnosed with H-TEF during the study period. Associated malformations were present in 43%, mostly cardiac (31%). The most frequent symptoms were cough (36%), bronchopneumonia (24%), and dysphagia (19%). H-TEF was detected by tracheobronchoscopy (90%), and/or upper GI (58%), and/or esophagoscopy (32%). The median age at diagnosis was 23 days (1 day–18 years). The most common approach was cervicotomy (76%), followed by thoracoscopy (14%) and thoracotomy (9%). The fistula underwent ligation and section of the fistula in 90% of the patients and clip closure and section in 9%. In one patient, the fistula was cauterized endoscopically. H-TEF preoperative cannulation was performed in 68% of cases, and a drain was placed in 26%. One month after surgery, 13% of the patients had mild persisting symptoms, mainly hypophonia. Recurrence occurred in 5%, and a second recurrence occurred in 1%. Conclusions: H-TEF prevalence was six cases/year, consistent with the expected rate of five cases/year in our country. The diagnosis was challenging, sometimes delayed, and, in most patients, required multiple examinations. Fistula ligation and section through cervicotomy were the most frequent treatment. Long-term outcomes are good, and recurrence is a rare event.

Publisher

MDPI AG

Reference29 articles.

1. Gross, R.E. (1953). Its Principles and Techniques, WB Saunders.

2. A fatal case of congenital tracheo-esophageal fistula;Lamb;Phila. Med. Times,1873

3. Esophageal atresia and tracheoesophageal fistula. A survey of its members by the surgical section of the American Academy of Pediatrics;Holder;Pediatrics,1964

4. Congenital tracheo-esophageal fistula without esophageal atresia;Helmsworth;J. Pediatr.,1951

5. Congenital H-type tracheoesophageal fistula in adults;Suen;J. Thorac. Dis.,2018

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