Patients With Congenital Choanal Atresia Treated by Transnasal Endoscopic Surgery

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dc.contributor.authorKinis, Vefa
dc.contributor.authorOzbay, Musa
dc.contributor.authorAkdag, Mehmet
dc.contributor.authorCetin, Muzeyyen
dc.contributor.authorGul, Aylin
dc.contributor.authorYilmaz, Beyhan
dc.contributor.authorSengul, Engin
dc.date.accessioned2024-04-24T17:08:29Z
dc.date.available2024-04-24T17:08:29Z
dc.date.issued2014
dc.departmentDicle Üniversitesien_US
dc.description.abstractCongenital choanal atresia (CCA) is defined as a congenital failure in the development of communication between the nasal cavity and nasopharynx in newborns. It is the most common congenital anomaly of nose. Most of the patients presented with unilateral CCA. Neonates with bilateral CCA have severe respiratory distress after birth. Airway control with orotracheal intubation should be done immediately to save the life of neonate with bilateral CCA. After airway control, surgery should be performed as soon as possible. The aim of surgery is to create a patent nasal passage and to prevent restenosis with minimal morbidity. Transnasal endoscopic surgery of CCA has become the most popular treatment method. The retrospective review of 33 patients with CCA was presented in this study. The patients who were diagnosed at the neonate period and operated on in 6 months after birth were grouped as I (neonate). The patients who were diagnosed 6 months after birth were grouped as II (child-young adult). All patients were treated by transnasal endoscopic surgery. Stent were put in all patients to prevent restenosis. Although the restenosis rate was higher in group I (53.8%) than in group II (23.1%), it did not cause a statistically significant difference. Overall success rate of our surgical approach was 61.5%. Despite the surgical developments and many treatment modalities, restenosis is still the most challenging problem in CCA.en_US
dc.identifier.doi10.1097/SCS.0000000000000541
dc.identifier.endpage897en_US
dc.identifier.issn1049-2275
dc.identifier.issn1536-3732
dc.identifier.issue3en_US
dc.identifier.pmid24657974
dc.identifier.scopus2-s2.0-84900863154
dc.identifier.scopusqualityQ3
dc.identifier.startpage892en_US
dc.identifier.urihttps://doi.org/10.1097/SCS.0000000000000541
dc.identifier.urihttps://hdl.handle.net/11468/17355
dc.identifier.volume25en_US
dc.identifier.wosWOS:000337098200077
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.ispartofJournal of Craniofacial Surgery
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCongenitalen_US
dc.subjectChoanal Atresiaen_US
dc.subjectNeonateen_US
dc.subjectTransnasalen_US
dc.subjectEndoscopic Surgeryen_US
dc.subjectRestenosisen_US
dc.titlePatients With Congenital Choanal Atresia Treated by Transnasal Endoscopic Surgeryen_US
dc.titlePatients With Congenital Choanal Atresia Treated by Transnasal Endoscopic Surgery
dc.typeArticleen_US

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