Outcomes of arterial switch operation for Taussig-Bing anomaly versus transposition of great arteries and ventricular septal defect

dc.contributor.authorErek, Ersin
dc.contributor.authorSuzan, Dilek
dc.contributor.authorAydin, Selim
dc.contributor.authorYildiz, Okan
dc.contributor.authorKirat, Baris
dc.contributor.authorDemir, I. Halil
dc.contributor.authorOdemis, Ender
dc.date.accessioned2023-02-21T12:34:20Z
dc.date.available2023-02-21T12:34:20Z
dc.date.issued2019-01-01
dc.description.abstractBackground: This study aims to present the outcomes of arterial switch operation for Taussig-Bing anomaly versus transposition of the great arteries and ventricular septal defect. Methods: Between November 2010 and December 2 016, a total of 100 consecutive arterial switch operations in 42 pediatric patients (25 males, 17 females
dc.description.abstractmedian age 17 days
dc.description.abstractrange, 2 to 210 days) were performed in two centers. Among them, 42 patients had associated ventricular septal defect and were diagnosed with Taussig-Bing anomaly (n=15) or transposition of the great arteries and ventricular septal defect (n=27). Aortic arch anomalies were present in six patients (40\%) with Taussig-Bing anomaly and two patients (7.4\%) with transposition of the great arteries and ventricular septal defect (p=0.016). Coronary anomaly was observed in five (33.3\%) and six (22.2\%) patients, respectively. All patient had a large defect (multiple n=4), except for eight patients who had moderate defect in the transposition of the great arteries group. Results: Early mortality was 13.3\% in the Taussig-Bing anomaly group and 7.4\% in the other group. Extracorporeal membrane oxygenation support was needed in three patients. Delayed sternal closure was used in most of the patients (92.9\%). The median length of intensive care unit and hospital stays were similar between the groups. The median follow-up was 16 (range, 1 to 50) months. Two patients including one planned (debanding and multiple defect closure) and one unplanned (residual defect closure) were reoperated. Three patients needed aortic balloon angioplasty due to recoarctation and one patient underwent pulmonary balloon angioplasty. Overall reintervention rate was 18.4\%. Conclusion: Although the incidence of aortic arch and coronary anomalies were higher in patients with Taussig-Bing anomaly, early and mid-term results were similar. Based on these results, primary arterial switch operation seems to be successfully performed for both pathologies.
dc.description.issue3
dc.description.issueJUL
dc.description.pages266-273
dc.description.volume27
dc.identifier.doi10.5606/tgkdc.dergisi.2019.17245
dc.identifier.urihttps://hdl.handle.net/11443/1719
dc.identifier.urihttp://dx.doi.org/10.5606/tgkdc.dergisi.2019.17245
dc.identifier.wosWOS:000474629300002
dc.publisherBAYCINAR MEDICAL PUBL-BAYCINAR TIBBI YAYINCILIK
dc.relation.ispartofTURK GOGUS KALP DAMAR CERRAHISI DERGISI-TURKISH JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY
dc.subjectCongenital heart disease
dc.subjectneonate
dc.subjectTaussig-Bing anomaly
dc.subjecttransposition of great arteries
dc.subjectventricular septal defect
dc.titleOutcomes of arterial switch operation for Taussig-Bing anomaly versus transposition of great arteries and ventricular septal defect
dc.typeArticle

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