Congenitally corrected transposition of the great arteries: outcomes after single ventricle palliation
摘要
Congenitally corrected transposition of the great arteries (ccTGA) is a rare congenital cardiac anomaly. As a viable alternative for complex anatomical variants, the outcomes of single-ventricle palliation (SVP) in ccTGA patients remain poorly defined.
MethodsWe conducted a single-center retrospective analysis of ccTGA patients who underwent SVP between January 2004 and December 2020.
ResultsA total of 73 patients were included. Patients with ccTGA undergoing SVP demonstrated excellent early and mid-term outcomes, with no observed mortality and freedom from MAEs of 96.0%, 93.6%, and 78.0% at 5, 10, and 15 years postoperatively, respectively.
ConclusionsSVP can achieve excellent early and mid-term outcomes in carefully selected ccTGA patients. When complex biventricular repair is not feasible, SVP represents a safe and effective alternative.
ImpactSingle-ventricle palliation can achieve excellent outcomes in selected congenitally corrected transposition of the great arteries. When complex biventricular repair is not feasible, SVP represents a safe and effective alternative.