Arterial switch. Mid-term follow up, eleven years of experience
pp 107-111
DOI:
https://doi.org/10.7775/rac.v73i2.3928Keywords:
Congenital heart disease, Cardiovascular surgical procedures/nursery, Transposition of the great vessels, Follow up studiesAbstract
Work objective
To evaluate the short and mid-term outcome after arterial switch operation in infants with transposition of the great arteries (TGA).
Research Design and Methods
Between 1992-2003, 122 patients were discharged from hospital after an arterial switch operation. One hundred and one patients were followed-up between 6 months and 11 years, median: 4 years. Morphologic features: Simple TGA: 75; TGA and VSD: 36; Taussing-Bing anomaly: 9; TGA + VSD and pulmonary stenosis: 2; an anatomic variant from the usual coronary artery pattern was noted in 17 patients (13.9%).
Results
All survivors remained in NHYA funcional class I. Supravalvular pulmonary stenosis was detected in 25 children (24.7%), considered severe in 10 (9.9%). Nine of these underwent surgery to relieve the pulmonary obstruction. A pulmonary angioplasty was later required in 2 patients. It was successful in one. Mild to moderate aortic incompetence was found in 2 patients (1.9%). It did no progress. Some degree of coronary artery obstruction was documented in 3 patients. Left ventricular systolic function remained whithin normal limits in all. One patient died as a result to a left coronary artery kinking, clearly shown on the previous angiogram.
Conclusions:
The short and mid-term evolution after the arterial switch operation for TGA is excellent with a survival rate of 99% up to 11 years of follow-up. Ninety nine percent of survivors remain in NYHA functional class I, keep on sinus rhythm and have a normal left ventricular systolic function. The most frequent complication was supravalvular pulmonary stenosis (24.7%), severe in only 8.9% and required treatment. Aortic incompetence was not important and did not progress. The only cause of late mortality was coronary artery obstruction.
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