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European Journal of Cardio-Thoracic Surgery, Vol 8, 651-656, Copyright © 1994 by European Association for Cardio-thoracic Surgery
A Kalangos, G Tayyareci, R Pretre, P Di Dio and O Sezerman
One hundred sixty-five patients undergoing primary myocardial
revascularization were prospectively entered into a randomized, double-
blind, placebo-controlled study, in a single institution, in order to
determine the influence of high- and low-dose aprotinin application on
early coronary artery bypass graft patency. All patients were operated on
by the same team and the three treatment groups were comparable in all
demographic data and surgical variables. Postoperative chest tube drainage
and transfusion requirements were significantly reduced in patients
receiving high or low doses of aprotinin. In all patients vein and internal
mammary artery graft patency was assessed by control coronary angiograms 4
to 15 days (median 8.2 days) postoperatively. In the high-dose aprotinin
group, 140 of 142 vein grafts and in the low- dose aprotinin group all of
the 128 vein grafts were patent compared with 138 of 139 in the placebo
group. The difference was not statistically significant (P > 0.05). All
pedicled internal mammary artery grafts were patent in the three treatment
groups. The prevalence of perioperative myocardial infarction was evaluated
by serial creatine kinase-myocardial band (CK-MB) isoenzyme measurements
and by electrocardiographic recordings. No additional changes that could be
attributed to aprotinin were observed. In conclusion, these results suggest
that perioperative myocardial infraction secondary to aprotinin- induced
native coronary artery or conduit thrombosis is not increased by aprotinin
in patients undergoing primary myocardial revascularization.
ARTICLES
Influence of aprotinin on early graft thrombosis in patients undergoing myocardial revascularization
Cardiovascular and Thoracic Surgery Center of Istanbul, Haydarpasa, Turkey.
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