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J Thorac Cardiovasc Surg 1995;110:1107-1117
© 1995 Mosby, Inc.
CARDIOPULMONARY BYPASS, |
Barcelona, Spain
Supported in part by Q. F. Bayer, Spain.
Received for publication Sept. 26, 1994. Accepted for publication March 15, 1995. Address for reprints: José Mateo, MD, Hematology Department, Hospital de Sant Pau, Av.P.Claret No. 167, 08025-Barcelona, Spain.
Abstract
Background. Aprotinin reduces blood loss in operations done with cardiopulmonary bypass, whereas the use of desmopressin remains controversial. We compared aprotinin, desmopressin, and placebo in a double-blind, randomized trial to evaluate bleeding and transfusion requirements. Methods and results.One hundred forty-nine patients (48 received aprotinin, 50 desmopressin, 51 placebo) were included. Blood loss and transfusion requirements were recorded and levels of Factor VIII coagulant activity, von Willebrand's factor, thrombin-antithrombin complexes, and D-dimer were measured. Overall blood loss was 195±146 ml/m 2in theaprotinin group, 400±192 ml/m 2in the desmopressingroup, and 489±361 ml/m 2in the placebo group (95% confidence intervals: difference between desmopressin and aprotinin 98 to 312 ml/m 2, p<0.001; difference betweenplacebo and aprotinin 190 to 398 ml/m 2, p<0.001). Twenty-six percent of patients treated with aprotinin, 66% of those treated with desmopressin, and 56% of those treated with placebo were given transfusion (95% confidence intervals: difference between aprotinin versus placebo plus desmopressin 51% to 71%, p<0.001). Fibrinolytic activation throughout cardiopulmonary bypass was markedly higher with placebo or desmopressin administration. D-dimer level correlated with overall blood loss in patients receiving desmopressin or placebo, but not in those receiving aprotinin.Conclusion. Aprotinin administration reduces blood loss and transfusion requirements in cardiopulmonary bypass. This benefit may be explained by a lower activation of fibrinolysis. (J THORAC CARDIOVASC SURG 1995;110:1107-17)
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