A comprehensive analysis of 51 neonates with congenital intestinal atresia

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dc.contributor.authorOzturk, Hayrettin
dc.contributor.authorOzturk, Hulya
dc.contributor.authorGedik, Senol
dc.contributor.authorDuran, Hatun
dc.contributor.authorOnen, Abdurrahman
dc.date.accessioned2024-04-24T17:33:10Z
dc.date.available2024-04-24T17:33:10Z
dc.date.issued2007
dc.departmentDicle Üniversitesien_US
dc.description.abstractObjective: To determine contemporary patterns of presentation and trends in the management and outcome of 51 newborn infants with intestinal atresia. Methods: We retrospectively reviewed 51 cases of intestinal atresia between January 1983 and February 2003. Clinical data included antenatal history, age, gender, weight, presenting symptoms and signs, diagnostic procedures, location and type of atresia, associated abnormalities, surgical treatment, associated problems, morbidity, mortality and plans of treatment. Results: Twenty children had duodenal obstruction, 24 had jejunoileal atresia, and 7 had colonic atresia. Approximately one-fourth of patients associated with duodenal atresia. had preterm delivery and all patients with jejunoileal and colonic atresia were full term. Clinical features such as vomiting, abdominal distention, delayed meconium passage and jaundice were more frequent in jejunoileal atresia patients. Other associated organ anomalies particularly Down's syndrome were more frequent in duodenal atresia patients. A duodeno-duodenostomy was preferred in most of the patients with duodenal atresia and annular pancreas; duodenotomy and web excision for those with duodenal webs; and resection with end-to-end anastomosis for those with jejunoileal atresia. In all patients with colonic atresia, colostomy procedure was performed as the first step of surgery. Conclusion: Experienced neonatal care and prompt total parenteral. nutrition by placing central line during surgery may improve the outcome of such patients.en_US
dc.identifier.endpage1054en_US
dc.identifier.issn0379-5284
dc.identifier.issue7en_US
dc.identifier.pmid17603708
dc.identifier.scopus2-s2.0-34548436885
dc.identifier.scopusqualityQ2
dc.identifier.startpage1050en_US
dc.identifier.urihttps://hdl.handle.net/11468/20499
dc.identifier.volume28en_US
dc.identifier.wosWOS:000248396500010
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.publisherSaudi Med Jen_US
dc.relation.ispartofSaudi Medical Journal
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[No Keyword]en_US
dc.titleA comprehensive analysis of 51 neonates with congenital intestinal atresiaen_US
dc.titleA comprehensive analysis of 51 neonates with congenital intestinal atresia
dc.typeArticleen_US

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