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dc.contributor.authorBilal, Mehmet Salih
dc.contributor.authorAvşar, Mustafa Kemal
dc.contributor.authorYıldırım, Özgür
dc.contributor.authorÖzyüksel, Arda
dc.contributor.authorZeybek, Cenap
dc.contributor.authorKüçükosmanoğlu, Osman
dc.contributor.authorDemiroluk, Şener
dc.date.accessioned10.07.201910:49:13
dc.date.accessioned2019-07-10T19:57:32Z
dc.date.available10.07.201910:49:13
dc.date.available2019-07-10T19:57:32Z
dc.date.issued2016en_US
dc.identifier.citationBilal, M. S., Avşar, M. K., Yıldırım, Ö., Özyüksel, A., Zeybek, C., Küçükosmanoğlu, O. ve Demiroluk, Ş. (2016). Double switch procedure and surgical alternatives for the treatment of congenitally corrected transposition of the great arteries. Journal Of Cardiac Surgery, 31(4), 231-236. https://dx.doi.org/10.1111/jocs.12728en_US
dc.identifier.issn0886-0440
dc.identifier.issn1540-8191
dc.identifier.urihttps://dx.doi.org/10.1111/jocs.12728
dc.identifier.urihttps://hdl.handle.net/20.500.12511/2998
dc.descriptionWOS: 000373615400011en_US
dc.descriptionPubMed ID: 26956686en_US
dc.description.abstractBackgroundWe present our experience with the double switch operation in sixteen patients with congenitally corrected transposition of the great arteries. MethodsWe enrolled 16 patients with congenitally corrected transposition of the great arteries operated by a single surgeon between 1995 and 2015. The mean age was 25 months (range 4 to 72 months) and the mean body weight was 8.9kg (range 4.3 to 19kg) at the time of operation. ResultsWe encountered seven patients with moderate to severe tricuspid regurgitation, five of which had Ebstein anomaly. We performed a combination of atrial and arterial switch procedures in 11 cases, one of which had a concomitant coarctation of the aorta that was repaired along with the double switch procedure. Atrial switch and the Rastelli procedures were performed in three cases with concomitant pulmonary stenosis. A combination of arterial switch, Hemi-Mustard procedure, and bidirectional cavopulmonary anastomosis was performed in two cases. During a mean follow-up period of 67 months (range three months to 18 years), we encountered one early postoperative mortality related to intracerebral bleeding. All but one of the patients are now in NYHA class I-II. ConclusionsCongenitally corrected transposition of the great arteries is a rare congenital cardiac anomaly in which the results of the anatomical repair with double switch operation appear to be superior to that achieved by a physiological repair. doi: 10.1111/jocs.12728 (J Card Surg 2016;31:231-236)en_US
dc.language.isoengen_US
dc.publisherWiley-Blackwellen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectDouble Switch Procedureen_US
dc.subjectSurgical Alternativesen_US
dc.subjectCongenitally Corrected Transpositionen_US
dc.subjectGreat Arteriesen_US
dc.titleDouble switch procedure and surgical alternatives for the treatment of congenitally corrected transposition of the great arteriesen_US
dc.typearticleen_US
dc.relation.journalJournal Of Cardiac Surgeryen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Kalp ve Damar Cerrahisi Ana Bilim Dalıen_US
dc.identifier.volume31en_US
dc.identifier.issue4en_US
dc.identifier.startpage231en_US
dc.identifier.endpage236en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1111/jocs.12728en_US


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