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The Journal of Thoracic and Cardiovascular Surgery, Vol 86, 832-837, Copyright © 1983 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
WI Norwood, P Lang, AR Castaneda and TJ Hougen
From January, 1975, through September, 1982, 24 infants underwent primary
or staged repair of interrupted aortic arch (IAA) with ventricular septal
defect (VSD). Seven patients had IAA type A and 17 patients had type B.
Eleven of the patients, median age 5 days, underwent staged operations and
13 infants, median age 6 days, underwent primary repair. Palliation was by
tube graft interposition (six), subclavian-aortic anastomosis (three), left
carotid-aortic anastomosis (one), or end-to-side aortic anastomosis (one)
combined with pulmonary artery banding (eight) or early VSD closure. With
palliation, there were three (27%) early deaths among the eleven patients
and one (13%) late death among the eight remaining. Delayed repair at 5
days to 14 months (median 7 months) in seven patients incurred three (43%)
early and no late deaths. Primary repair in 13 patients consisted of VSD
closure combined with graft interposition (12) or end-to-side aortic
anastomosis (one), with three (23%) early and no late deaths. Nine of 14
survivors had hemodynamic evaluation by catheterization 1 to 3 years
following repair. None had a significant residual VSD or pressure gradients
between the ascending and thoracic aorta. Six had subaortic stenosis, two
mild (gradient less than 20 mm Hg) and four severe (gradient greater than
50 mm Hg), necessitating operation. Results of operations in neonates with
IAA continue to improve. Essential in management is an awareness that
subaortic stenosis and hypocalcemia may be accompaniments of this anomaly.
Based on these data, we prefer primary repair for IAA with VSD.
ARTICLES
Reparative operations for interrupted aortic arch with ventricular septal defect
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