Transposition of the great arteries (TGA) covers a wide range of anatomic v
ariants involving not only the origin of the great arteries, but the intrac
ardiac structures and the aortic arch. TGA can now benefit from complete an
atomic repair, namely switch operation, performed in simple forms during th
e neonatal period Accurate pre and intraoperative assessment must take into
account the main anatomic features: relationship between the aorta and the
pulmonary artery and coronary arteries distribution. Over the last sixteen
years, 1 063 patients with TGA underwent anatomic repair in our institutio
n. Among 728 patients with simple TGA, 92 % were operated on within the fir
st 2 weeks of life. Among 335 patients with complex TGA, all had a large VS
D and 154 had additional anomalies. Among these 335 patients, 264 had one-s
tage complete repair. and 71 had two-stage repair, at the beginning of our
experience. In complex forms the main associated anomalies involved the ven
tricles (right ventricle hypoplasia (II), malaligned VSD (90), restrictive
VSD (3), multiple VSD (43)), the atrioventricular valves (straddling of the
mitral or tricuspid valve (15), mitral valve anomalies (cleft or tissue ta
g. 4) mid the aortic arch (coarctation [88], interrupted aortic arch (8)).
The hospital mortality was 6.9 % for simple TGA, 14.6 % for complex TGA. Ma
in causes of early death were failure in coronary artery relocation and pul
monary hypertensive crisis, Mean follow-up (95.5 % of patients) was 49 mont
hs. Overall 16-year survival was 87.9 %, 91,5 % for simple forms and 80.4 %
for complex forms Anatomic repair is nowadays the treatment of choice for
TGA. Long-term results will depend on the evolution of the relocated corona
ry arteries and of the neo-aortic valve.