A comprehensive analysis of 51 neonates with congenital intestinal atresia

dc.authorid0000-0001-5608-5742
dc.authorid0000-0003-1719-4924
dc.authorid0000-0003-1671-4094
dc.contributor.authorÖztürk, Hayrettin
dc.contributor.authorÖztürk, Hülya
dc.contributor.authorGedik, Şenol
dc.contributor.authorDuran, Hatun
dc.contributor.authorÖnen, Abdurrahman
dc.date.accessioned2021-06-23T19:20:08Z
dc.date.available2021-06-23T19:20:08Z
dc.date.issued2007
dc.departmentBAİBÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_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.pmid17603708en_US
dc.identifier.scopus2-s2.0-34548436885en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage1050en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12491/6065
dc.identifier.urihttps://smj.org.sa/content/smj/28/7/1050.full.pdf
dc.identifier.volume28en_US
dc.identifier.wosWOS:000248396500010en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.institutionauthorÖztürk, Hayrettin
dc.institutionauthorÖztürk, Hülya
dc.language.isoenen_US
dc.publisherSaudi Med Jen_US
dc.relation.ispartofSaudi Medical Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCongenital Intestinal Atresiaen_US
dc.titleA comprehensive analysis of 51 neonates with congenital intestinal atresiaen_US
dc.typeArticleen_US

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