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The Annals of Thoracic Surgery, Vol 40, 360-364, Copyright © 1985 by The Society of Thoracic Surgeons
PH Kay and DN Ross
Ninety-seven patients with pulmonary atresia underwent right ventricular
outflow tract reconstruction using a homograft conduit. There were 46
hospital deaths (47%). Hospital mortality was significantly related to
irreversible pulmonary hypertension (p less than 0.001) and thoracotomy for
ligation of bronchial collaterals (p less than 0.01). The actuarial
survival was 37 +/- 7% at 10 years. Sixteen patients undergoing
recatheterization at a mean of 6 years had a mean transconduit gradient of
24 +/- 15 mm Hg. Obstructed conduits (i.e., with a gradient of greater than
50 mm Hg) were replaced in 3 patients, corresponding to 13 +/- 8% at 10
years. In each instance, the obstruction was due to neointimal hyperplasia
in the Dacron tube rather than calcification of the homograft valve. The
fresh, antibiotic- sterilized aortic homograft is the conduit of choice for
right ventricular outflow tract reconstruction. The valve itself appears
more resistant to calcification than its xenograft counterpart, and the
absence of Dacron removes the problem of fibrinous peel obstructing the
conduit. We now construct a tube of autologous pericardium to increase the
length of the conduit and avoid complementary thoracotomy for ligation of
bronchial collaterals.
ARTICLES
Fifteen years' experience with the aortic homograft: the conduit of choice for right ventricular outflow tract reconstruction
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