Markers of Hypercoagulability in Patients with Hemophilia B Given Repeated, Large Doses of Factor IX Concentrates during and after Surgery

Author:

Santagostino E12,Mannucci P M12,Gringeri A12,Tagariello G32,Baudo F42,Bauer K A52,Rosenberg R D52

Affiliation:

1. Angelo Bianchi Bonomi Hemophilia and Thrombosis Center and Institute of Internal Medicine, IRCCS Maggiore Hospital and University of Milan, Italy

2. Department of Medicine, Beth Israel Hospital and Harvard Medical School Boston, MA, USA

3. Transfusion Center, Castelfranco, Veneto, Italy

4. Hematology Division, Ca Granda Hospital, Milan, Italy

5. Charles A. Dana Research Institute and the Harward-Thorndike Laboratory, Boston, MA, USA

Abstract

SummaryPurer factor IX (FIX) concentrates have been produced for the treatment of hemophilia B in the attempt to reduce the risk of thrombotic complications associated with the use of prothrombin complex concentrates. To evaluate ex vivo whether or not FIX concentrates activate the coagulation system in conditions associated with a high risk for thrombosis, we measured markers of hypercoagulability in 10 patients with hemophilia B who underwent surgery, mainly orthopedic procedures, covered by multiple concentrate infusions (40-80 U/kg/day). Postinfusion plasma levels of prothrombin fragment 1+2 and factor X activation peptide did not differ significantly from the presurgical levels, neither before nor after each concentrate dose. Therefore, it appears that prolonged treatment of patients with hemophilia B undergoing high risk surgical procedures with high doses of FIX concentrate does not cause systemic activation of coagulation. This suggests that purified FIX concentrates are preferable to prothrombin complex concentrates for conditions associated with an increased risk of thrombosis.

Publisher

Georg Thieme Verlag KG

Subject

Hematology

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