Abstract
Background: The surgical concepts for patients with congenitally corrected transposition of the
great arteries (CCTGA) address discordant connections and associated lesions. The
outcomes after biventricular repair without correction of discordant connections (“classic
repair”, or with its correction “anatomic repair”) and after “univentricular palliation”
were investigated. Methods: All patients with CCTGA who underwent “classic repair” (n = 39), “anatomic repair”
(n = 6), or “univentricular palliation” (n = 11) between 1978 and 2006 were analyzed.
The most frequently associated lesions were ventricular septal defect (n = 48), tricuspid
insufficiency (TI) (n = 20) and functionally single ventricle (n = 11). Results: Thirty-day mortality was 4 % (2/56). Mean follow-up for early survivors was 7.2 ± 7.1
years. Eight patients died late, two after heart transplantation. Survival was not
significantly different between patients who underwent “anatomic” or “classic repair”,
or “univentricular palliation”: 83.3 ± 15.2 %, 79.7 ± 6.9 %, 90.9 ± 8.7 % at 10 years,
respectively. In multivariate analysis, the presence of TI emerged as the only risk
factor for late death (p = 0.004). Twenty patients required reoperation, mainly for TI (n = 10) and conduit
failure (n = 6). Freedom from reoperation was lower after “anatomic repair”, but ventricular
function was better and atrioventricular valves were more competent than after “classic
repair”. Conclusions: Biventricular “anatomic” or “classic repair” and “univentricular palliation” yield
equivalent survival rates in the mid-term. Biventricular “anatomic repair”, when feasible,
should be promoted because of its better long-term outcome.
Key words
cardiovascular surgery - congenital heart disease - great vessel anomalies
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1 Both authors contributed equally to the study.
Dr. Jürgen Hörer
Department of Cardiovascular Surgery
German Heart Center Munich at the Technical University
Lazarettstraße 36
80636 Munich
Germany
Phone: + 49 (0) 89 12 18 41 11
Fax: + 49 (0) 89 12 18 41 23
Email: hoerer@dhm.mhn.de