Surgical correction of cor triatriatum sinister in the paediatric population: mid-term results in 15 cases

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dc.authorid0000-0001-7478-6235
dc.contributor.authorÖzyüksel, Arda
dc.contributor.authorYıldırım, Özgür
dc.contributor.authorAvşar, Mustafa Kemal
dc.contributor.authorHayırlıoğlu, Mehmet
dc.contributor.authorDemiroluk, Şener
dc.contributor.authorKüçükosmano?lu, Osman
dc.contributor.authorBilal, Mehmet Salih
dc.date.accessioned10.07.201910:49:13
dc.date.accessioned2019-07-10T19:52:26Z
dc.date.available10.07.201910:49:13
dc.date.available2019-07-10T19:52:26Z
dc.date.issued2015
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Kalp ve Damar Cerrahisi Ana Bilim Dalı
dc.descriptionWOS: 000352166800006
dc.descriptionPubMed ID: 25312520
dc.description.abstractOBJECTIVES: Cor triatriatum sinister (CTS) is a rare developmental cardiac abnormality resulting in left ventricular inflow obstruction. In this report, we aimed to present our mid-term results of early childhood patients operated for CTS and associated cardiac abnormalities. METHODS: We enrolled 15 patients with CTS who were operated by a single surgeon between 2001 and 2013. A retrospective analysis was performed in order to determine the demographics, operative and postoperative results of the patients. The median age was 14 months and the median body weight was 8.2 kg at the time of operation. RESULTS: Fourteen patients had concomitant cardiac pathology. Three of the patients had atrial septal defect and 1 of the patients had partial abnormal pulmonary venous connection, whereas 4 of the patients had both. In 2 cases of complete atrioventricular septal defect, 1 case with ventricular septal defect, 1 case with patent ductus arteriosus, 1 case with double outlet right ventricle and another case with tetralogy of Fallot, complete repair was performed together with membrane resection in the left atrium (LA). The mean preoperative left atrial gradient was 13.3 mmHg, whereas the mean LA pressure at the first postoperative year was 4.2 mmHg. There was 1 case with early mortality due to septic multiorgan failure secondary to pneumonia. CONCLUSIONS: CTS is a rare congenital cardiac anomaly in which the results of the corrective surgery are encouraging. Early and long-term outcomes may be variable according to the associated congenital heart defects.
dc.identifier.citationÖzyüksel, A., Yıldırım, Ö., Avşar, M. K., Hayırlıoğlu, M., Demiroluk, Ş., Küçükosmano?lu, O. ve Bilal, M. S. (2015). Surgical correction of cor triatriatum sinister in the paediatric population: mid-term results in 15 cases. European Journal of Cardio-Thoracic Surgery, 47(1), e25-e28. https://dx.doi.org/10.1093/ejcts/ezu390
dc.identifier.doi10.1093/ejcts/ezu390
dc.identifier.endpagee28
dc.identifier.issn1010-7940
dc.identifier.issn1873-734X
dc.identifier.issue1
dc.identifier.startpagee25
dc.identifier.urihttps://dx.doi.org/10.1093/ejcts/ezu390
dc.identifier.urihttps://hdl.handle.net/20.500.12511/2402
dc.identifier.volume47
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherOxford University Press
dc.relation.ispartofEuropean Journal of Cardio-Thoracic Surgeryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCor Triatriatum Sinister
dc.subjectCongenital Heart Defects
dc.subjectCardiac Surgery
dc.titleSurgical correction of cor triatriatum sinister in the paediatric population: mid-term results in 15 cases
dc.typeArticle

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