Prevalence and natural history of scoliosis and associated congenital vertebral anomalies in patients operated for esophageal atresia with or without tracheoesophageal fistula.


Journal

Journal of pediatric surgery
ISSN: 1531-5037
Titre abrégé: J Pediatr Surg
Pays: United States
ID NLM: 0052631

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 13 04 2018
revised: 16 08 2018
accepted: 29 08 2018
pubmed: 12 10 2018
medline: 5 11 2019
entrez: 11 10 2018
Statut: ppublish

Résumé

Scoliosis has been reported after repair of esophageal atresia with or without tracheoesophageal fistula (EA-TEF). This study aims to investigate the prevalence and natural history of scoliosis and associated congenital vertebral anomalies in patients operated for EATEF. A retrospective review of patients operated for EA-TEF with radiological examination for the presence of scoliosis or associated spine congenital anomalies was done on 106 patients (ages 5-19 years). Scoliosis was found in 53 patients (49%) for which 46 of these were in the thoracic region and 33 were right-thoracic curves. After a follow-up ranging from 5 to 14 years, four patients (3.7%) out of 106 were operated for scoliosis. Right-sided thoracotomy (RST) was the identifiable risk factor for scoliosis development; all patients with scoliosis had their EA repaired through RST. Congenital vertebral anomalies were found in 8 of those patients (7.5%). After a median follow-up of 6.5 years, no patients progressed enough to require operation. Scoliosis affects one of every two patients operated for EA; it may progress to the indication of surgery. RST was the identifiable risk factor for scoliosis development.

Sections du résumé

BACKGROUND BACKGROUND
Scoliosis has been reported after repair of esophageal atresia with or without tracheoesophageal fistula (EA-TEF). This study aims to investigate the prevalence and natural history of scoliosis and associated congenital vertebral anomalies in patients operated for EATEF.
METHODS METHODS
A retrospective review of patients operated for EA-TEF with radiological examination for the presence of scoliosis or associated spine congenital anomalies was done on 106 patients (ages 5-19 years).
RESULTS RESULTS
Scoliosis was found in 53 patients (49%) for which 46 of these were in the thoracic region and 33 were right-thoracic curves. After a follow-up ranging from 5 to 14 years, four patients (3.7%) out of 106 were operated for scoliosis. Right-sided thoracotomy (RST) was the identifiable risk factor for scoliosis development; all patients with scoliosis had their EA repaired through RST. Congenital vertebral anomalies were found in 8 of those patients (7.5%). After a median follow-up of 6.5 years, no patients progressed enough to require operation.
CONCLUSION CONCLUSIONS
Scoliosis affects one of every two patients operated for EA; it may progress to the indication of surgery. RST was the identifiable risk factor for scoliosis development.

Identifiants

pubmed: 30301608
pii: S0022-3468(18)30556-6
doi: 10.1016/j.jpedsurg.2018.08.049
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1308-1311

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Hany Ag Soliman (HA)

University of Montreal, Montreal, Canada; CHU Sainte-Justine, Montreal, Canada; Al-Azhar University, Al Zahraa University Hospital, Egypt.

Christophe Faure (C)

University of Montreal, Montreal, Canada; CHU Sainte-Justine, Montreal, Canada.

Geneviève Berubé (G)

University of Sherbrooke, Sherbrooke, Canada.

Jean-Marc Mac-Thiong (JM)

University of Montreal, Montreal, Canada; CHU Sainte-Justine, Montreal, Canada; Hôpital du Sacré-Coeur, Montreal, Canada.

Soraya Barchi (S)

CHU Sainte-Justine, Montreal, Canada.

Stefan Parent (S)

University of Montreal, Montreal, Canada; CHU Sainte-Justine, Montreal, Canada; Hôpital du Sacré-Coeur, Montreal, Canada. Electronic address: stefan.parent@umontreal.ca.

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Classifications MeSH