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dc.contributor.authorShija, J. K.
dc.date.accessioned2019-06-03T11:58:27Z
dc.date.accessioned2019-10-04T00:41:40Z
dc.date.available2019-06-03T11:58:27Z
dc.date.available2019-10-04T00:41:40Z
dc.date.issued1976-06
dc.identifier.citationShija, J. K. (1976). Congenital atresia of the oesophagus. Medical Journal of Zambia. 10, (3)en
dc.identifier.urihttps://library.adhl.africa/handle/123456789/11668
dc.descriptionManagement of Congenital Esophageal Atresiaen
dc.description.abstractExperiences elsewhere in well-established Specialist Centres have shown that the management of Congenital Oesophageal Atresia is beset with many problems, including serious post-operative complications , and that this anomaly carries a high mortality (Cozzi & Wilkinson,1975).During january-December 1975, the first year of its existence, the newly-established Paediatric Surgical Unit at Muhimbili Hospital, Dar es Salaam,has had 2 cases of Oesophageal Atresia referred to it from the Neonatal Unit for treatment. The first case(F.N.) was, in spite of the late diagnosis, a total success (the first such success reported at this hospital), and the patient was last seen alive and well at the age of 9 months; the second case also had successful surgery but succumbed on the 11 th postoperative day due to intractable pulmonary complications. The problems faced and experience gained in the management of these cases are discussed.en
dc.description.sponsorshipOffice of Global AIDS/US Department of Stateen
dc.language.isoenen
dc.publisherMedical Journal of Zambiaen
dc.relation.ispartofseriesVol.10;(3)
dc.subjectPulmonary Complicationsen
dc.subjectEsophageal Atresiaen
dc.subjectSpecialties, Surgicalen
dc.titleCongenital atresia of the oesophagusen
dc.typeArticleen


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