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The Journal of Thoracic and Cardiovascular Surgery, Vol 116, 770-779, Copyright © 1998 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
CP Brizard, C Mas, YS Sohn, AD Cochrane and TR Karl
OBJECTIVES: The study's object was to analyze the outcomes of
transatrial-transpulmonary repair in children with tetralogy of Fallot and
anomalous coronary artery crossing the right ventricular outflow tract.
METHODS: The transatrial-transpulmonary approach was used in 611
consecutive repairs, 36 (5.9%) of which were associated with a surgically
relevant coronary artery anomaly. The median age and weight of the patients
at repair were 23 months (2.8-170 months) and 9.9 kg (5.2-41 kg),
respectively. Anomalies included left anterior descending coronary artery
from right coronary artery or single right coronary artery (n = 22), right
coronary artery from left coronary artery or left anterior descending
coronary artery (n = 8), and large right coronary artery conal branch (n =
6). Diagnosis was established before the operation in 25 of 36 cases by
angiography (n = 24) or echocardiography (n = 1). The approach was
successful in 34 cases, in 25 of which placement of a limited transannular
patch was necessary. Two patients had a right ventricle-pulmonary artery
conduit as a result of proximity of the coronary branch to the pulmonary
arterial anulus and inability to adequately relieve the right ventricular
outflow tract obstruction. RESULTS: There have been no early or late
deaths. Mean right ventricle-pulmonary artery gradient at last follow-up
was 19 mm Hg (95% confidence interval 14.5-24 mm Hg), compared with 15 mm
Hg (95% confidence interval 12.5-17.5 mm Hg) for patients with normal
coronary arteries (P = .3). Actuarial freedom from reoperation at 120
months was 96.5% (95% confidence interval 79.8%-99.5%) and was also similar
between patients with and without coronary artery abnormalities (P = .92).
CONCLUSIONS: Surgically important coronary anomalies in tetralogy of Fallot
can be dealt with through the transatrial-transpulmonary approach in most
cases without major alterations in technique. Outcomes are similar to those
of other patients with tetralogy of Fallot. The presence of anomalous
coronary arteries does not impart incremental risk after this surgical
strategy.
ARTICLES
Transatrial-transpulmonary tetralogy of Fallot repair is effective in the presence of anomalous coronary arteries
Victorian Paediatric Cardiac Surgical Unit, Royal Children's Hospital, Melbourne, Australia.
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