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dc.date.accessioned2013-03-12T12:37:02Z
dc.date.available2016-11-22T23:30:34Z
dc.date.issued2011en_US
dc.date.submitted2011-11-18en_US
dc.identifier.citationMeland, Trond. Congenital Malformations of the Aortic Arch and Isthmus. Prosjektoppgave, University of Oslo, 2011en_US
dc.identifier.urihttp://hdl.handle.net/10852/29347
dc.description.abstractBakcground: This quality-control study includes patients operated for Coarctation of the Aorta or Interrupted Aortic Arch at Rikshospitalet between 1971 and 2001 to give a comprehensive presentation of the material and identify predictors for death and for re-operation free survival Methods: 588 patients were identified, information was obtained from databases, registries and patient records, then analyzed with Kaplan-Meier, univariate and multivariate regression analysis to identify risk factors. Results: Fwup completeness was (99,3%), median fwup time was 19,15 years. There were 348 boys (59,2%) and 240 girls (40,8%), 425 had isolated CoA (72,2%), 108 had hypoplasia (18,4%), 55 had IAA (9,4%) Age at initial repair was <1 month in 244 (41,5%), between 1 month and one year in 126 (21,4%), >1 year in 218 (37,1%). 330 was considered to be in comorbidity group I (56,1%), 130 in group II (22,1%), 128 in comorbidity group III (21,8%) There were 59 early deaths (9,4%) and a total mortality of 20,6%. Operation in early time period, comorbidity group III, median sternotomy approach and surgery in the neonatal period predicted death. 113 patients (19,2%) were re-operated at a median time of 8,09 years after initial surgery. Re-operation free survival was 55% 30-35 after inital repair. Risk factors for death or re-operation was early time period, hypoplasia, interrupted arch, group III comorbidity and repair at neonatal age. Conclusions: Mortality after surgical repair of Coa and IAA is linked to coexisting cardiac malformations. Hypoplasia of the aortic arch strongly predispose for re-operation.eng
dc.language.isoengen_US
dc.subjectkirurgi
dc.titleCongenital Malformations of the Aortic Arch and Isthmus : A retrospective study of 588 patients undergoing surgery for Aortic Coarctation or Interrupted Aortic Arch at Rikshospitalet from 1971 to 2001en_US
dc.typeMaster thesisen_US
dc.date.updated2011-12-22en_US
dc.creator.authorMeland, Tronden_US
dc.subject.nsiVDP::780en_US
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft.au=Meland, Trond&rft.title=Congenital Malformations of the Aortic Arch and Isthmus&rft.inst=University of Oslo&rft.date=2011&rft.degree=Prosjektoppgaveen_US
dc.identifier.urnURN:NBN:no-29865en_US
dc.type.documentProsjektoppgaveen_US
dc.identifier.duo143095en_US
dc.contributor.supervisorHarald L. Lindbergen_US
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/29347/2/Prosjekt-Meland.pdf


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