Post-Operative Prognosis of the Patients with Esophageal Atresia: The 22-Year Experience of a Reference Hospital

dc.contributor.authorBAKAL, U.
dc.contributor.authorERSOZ, F.
dc.contributor.authorSARAC, M.
dc.contributor.authorAYDIN, M.
dc.contributor.authorTARTAR, T.
dc.contributor.authorORMAN, A.
dc.contributor.authorKAZEZ, A.
dc.date.accessioned2026-08-12T17:07:00Z
dc.date.issued2022
dc.departmentFırat Üniversitesi
dc.description.abstractIntroduction: To investigate the post-operative prognosis of newborns with esophageal atresia (EA). Methods: Patients operated for EA were classified according to their gestational age, birth-weight, gender, and study period (1996-2006 & 2007-2017), type of atresia, accompanying additional anomaly and Waterston risk categories. Results: Of the 87 cases, 87.4% had EA + distal tracheoesophageal fistula, 11.5% had isolated EA and 1.1% had isolated tracheoesophageal fistula. While 36.8% patients developed post-operative complications, 37% patients died. There was a statistically significant difference between full-term and preterm newborns in terms of mortality rate (p<0.05). Most of dead cases had low birth-weight of <2500 g (n=28/55). Mortality rates of the patients with EA according to two study periods were 57% and 22%, respectively. Main causes of mortality were sepsis (n=17), pneumonia (n=9), and respiratory failure (n=6). Mortality rate among those had accompanying additional anomaly was 84.4% (p<0.05). There was a significant difference between Waterston's risk classification (Groups C and B) and post-operative complication, and mortality rates (p<0.05). In those surviving cases, the most common long-term complication was dysphagia (83%). Conclusion: Morbidity and mortality rates of patients with EA in developing countries like to our study are still high. Low birth-weight, accompanying additional anomaly, Waterston Groups C and B, and post-operative complications are the most important causes of mortality. Waterston's risk classification is a good predictor of the prognosis in patients with EA.
dc.identifier.endpage169
dc.identifier.issn1013-9923
dc.identifier.issue3
dc.identifier.orcid0000-0003-1783-0185
dc.identifier.scopus2-s2.0-85134363679
dc.identifier.scopusqualityQ4
dc.identifier.startpage163
dc.identifier.urihttps://hdl.handle.net/11508/49459
dc.identifier.volume27
dc.identifier.wosWOS:000829093900002
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherMedcom Ltd
dc.relation.ispartofHong Kong Journal of Paediatrics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectClassification
dc.subjectEsophageal atresia
dc.subjectMortality
dc.subjectPrognosis
dc.subjectSurgery
dc.subjectTracheoesophageal fistula
dc.titlePost-Operative Prognosis of the Patients with Esophageal Atresia: The 22-Year Experience of a Reference Hospital
dc.typeArticle

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