Delayed diagnosis: An important prognostic factor for oesophageal atresia in developing countries

dc.contributor.authorKarakus, Suleyman Cuneyt
dc.contributor.authorOzokutan, Bulent Hayri
dc.contributor.authorBakal, Unal
dc.contributor.authorCeylan, Haluk
dc.contributor.authorSarac, Mehmet
dc.contributor.authorKul, Seval
dc.contributor.authorKazez, Ahmet
dc.date.accessioned2026-08-12T17:17:03Z
dc.date.issued2016
dc.departmentFırat Üniversitesi
dc.description.abstractAim: The aim of this study is to analyse the effect of delayed diagnosis on mortality rates, and evaluate the role of delayed diagnosis as a new prognostic factor in patients with oesophageal atresia (OA), especially in developing countries. Methods: The records of 80 consecutive patients with OA (2008-2013) were reviewed. Patients were divided into two groups according to the time of diagnosis. As we demonstrated the effect of delayed diagnosis on mortality, we decided to develop a new classification that will be utilised to predict the prognosis of OA. The discrimination ability of the new prognostic classification was compared with those of the Waterston, Montreal and Spitz classifications using the area under the curve. Results: The parameters of the new prognostic classification were birth weight less than 2000 g, the presence of major cardiac/life-threatening anomalies and delay in diagnosis. Class I consisted of patients with none or one of these parameters. Class II consisted of patients with two or three of these parameters. The area under the curve of the new classification was better than those of the other classifications in determining the prognosis of patients with OA. Conclusions: Delayed diagnosis of OA significantly led to morbidity and mortality. Although delayed diagnosis is not a characteristic of newborn or a marker of severity for OA and is a health care system issue in developing countries, we here point out that it is a prognostic factor in its own right. Our new classification has a superior discriminatory ability compared to the above-mentioned classifications.
dc.identifier.doi10.1111/jpc.13354
dc.identifier.endpage1094
dc.identifier.issn1034-4810
dc.identifier.issn1440-1754
dc.identifier.issue12
dc.identifier.orcid0000-0002-5140-8618
dc.identifier.pmid27701787
dc.identifier.scopus2-s2.0-84994749757
dc.identifier.scopusqualityQ2
dc.identifier.startpage1090
dc.identifier.urihttps://doi.org/10.1111/jpc.13354
dc.identifier.urihttps://hdl.handle.net/11508/52523
dc.identifier.volume52
dc.identifier.wosWOS:000391969800009
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley-Blackwell
dc.relation.ispartofJournal of Paediatrics and Child Health
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjecthealth policy
dc.subjectoesophageal congenital anomalies
dc.subjectoesophageal surgery
dc.subjectoutcomes
dc.titleDelayed diagnosis: An important prognostic factor for oesophageal atresia in developing countries
dc.typeArticle

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