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

congenital tracheoesophageal fistula h-type esophageal atresia type E esophageal atresia

Journal

Children (Basel, Switzerland)
ISSN: 2227-9067
Titre abrégé: Children (Basel)
Pays: Switzerland
ID NLM: 101648936

Informations de publication

Date de publication:
02 Apr 2024
Historique:
received: 18 02 2024
revised: 12 03 2024
accepted: 29 03 2024
medline: 27 4 2024
pubmed: 27 4 2024
entrez: 27 4 2024
Statut: epublish

Résumé

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. 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). 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%. 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.

Sections du résumé

BACKGROUND 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 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 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 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.

Identifiants

pubmed: 38671640
pii: children11040423
doi: 10.3390/children11040423
pii:
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Cecilia Morchio (C)

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

Alba Ganarin (A)

Pediatric Surgery Unit, Ca' Foncello Hospital, 31100 Treviso, Italy.

Andrea Conforti (A)

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

Ernesto Leva (E)

Pediatric Surgery Unit, Fondazione IRCCS Ca' Granda-Ospedale Maggiore Policlinico, University of Milan, 20100 Milan, Italy.

Giovanni Gaglione (G)

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

Gaia Brenco (G)

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

Elisa Zambaiti (E)

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

Salvatore Fabio Chiarenza (SF)

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

Tamara Caldaro (T)

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

Maurizio Cheli (M)

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

Giovanni Boroni (G)

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

Elena Sofia Marcandella (ES)

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

Giovanna Riccipetitoni (G)

Department of Paediatric Surgery, "V. Buzzi" Children's Hospital, 20100 Milan, Italy.
Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, Fondazione IRCCS Policlinico San Matteo, 27100 Pavia, Italy.

Sebastiano Cacciaguerra (S)

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

Vincenzo Di Benedetto (V)

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

Valerio Gentilino (V)

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

Gabriele Lisi (G)

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

Francesco Morini (F)

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

Paola Midrio (P)

Pediatric Surgery Unit, Ca' Foncello Hospital, 31100 Treviso, Italy.

Classifications MeSH