A Comparison of Aprotinin and Lysine Analogues in High-Risk Cardiac Surgery

Dean Fergusson(University of Ottawa), Paul C. Hébert(University of Ottawa), C. David Mazer(University of Toronto), Stephen E. Fremes(University of Toronto), Charles MacAdams(Libin Cardiovascular Institute of Alberta), John M. Murkin(Western University), Kevin Teoh(Health Sciences Centre), Peter C. Duke(Health Sciences Centre), Ramiro Arellano(Queen's University), Morris A. Blajchman(McMaster University), Jean S. Bussières(Institut Universitaire de Cardiologie et de Pneumologie de Québec), Dany Côté(Institut Universitaire de Cardiologie et de Pneumologie de Québec), Jacek Karski(Toronto General Hospital), Raymond Martineau(Montreal Heart Institute), James A. Robblee(University of Ottawa), Marc Rodger(University of Ottawa), George A. Wells(University of Ottawa), Jennifer Clinch, Roanda Pretorius
New England Journal of Medicine
May 14, 2008
Cited by 1,144Open Access
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Abstract

BACKGROUND: Antifibrinolytic agents are commonly used during cardiac surgery to minimize bleeding and to reduce exposure to blood products. We sought to determine whether aprotinin was superior to either tranexamic acid or aminocaproic acid in decreasing massive postoperative bleeding and other clinically important consequences. METHODS: In this multicenter, blinded trial, we randomly assigned 2331 high-risk cardiac surgical patients to one of three groups: 781 received aprotinin, 770 received tranexamic acid, and 780 received aminocaproic acid. The primary outcome was massive postoperative bleeding. Secondary outcomes included death from any cause at 30 days. RESULTS: The trial was terminated early because of a higher rate of death in patients receiving aprotinin. A total of 74 patients (9.5%) in the aprotinin group had massive bleeding, as compared with 93 (12.1%) in the tranexamic acid group and 94 (12.1%) in the aminocaproic acid group (relative risk in the aprotinin group for both comparisons, 0.79; 95% confidence interval [CI], 0.59 to 1.05). At 30 days, the rate of death from any cause was 6.0% in the aprotinin group, as compared with 3.9% in the tranexamic acid group (relative risk, 1.55; 95% CI, 0.99 to 2.42) and 4.0% in the aminocaproic acid group (relative risk, 1.52; 95% CI, 0.98 to 2.36). The relative risk of death in the aprotinin group, as compared with that in both groups receiving lysine analogues, was 1.53 (95% CI, 1.06 to 2.22). CONCLUSIONS: Despite the possibility of a modest reduction in the risk of massive bleeding, the strong and consistent negative mortality trend associated with aprotinin, as compared with the lysine analogues, precludes its use in high-risk cardiac surgery. (Current Controlled Trials number, ISRCTN15166455 [controlled-trials.com].).


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