期刊论文详细信息
Reversal of Rivaroxaban and Dabigatran by Prothrombin Complex Concentrate A Randomized, Placebo-Controlled, Crossover Study in Healthy Subjects
Article
关键词: THROMBIN INHIBITOR DABIGATRAN;    FACTOR-XA INHIBITOR;    RECOMBINANT FACTOR VIIA;    TOTAL HIP;    GENERATION;    WARFARIN;    PHARMACODYNAMICS;    PHARMACOKINETICS;    ETEXILATE;    PROFILE;   
DOI  :  10.1161/CIRCULATIONAHA.111.029017
来源: SCIE
【 摘 要 】

Background-Rivaroxaban and dabigatran are new oral anticoagulants that specifically inhibit factor Xa and thrombin, respectively. Clinical studies on the prevention and treatment of venous and arterial thromboembolism show promising results. A major disadvantage of these anticoagulants is the absence of an antidote in case of serious bleeding or when an emergency intervention needs immediate correction of coagulation. This study evaluated the potential of prothrombin complex concentrate (PCC) to reverse the anticoagulant effect of these drugs. Methods and Results-In a randomized, double-blind, placebo-controlled study, 12 healthy male volunteers received rivaroxaban 20 mg twice daily (n=6) or dabigatran 150 mg twice daily (n=6) for 2 1/2 days, followed by either a single bolus of 50 IU/kg PCC (Cofact) or a similar volume of saline. After a washout period, this procedure was repeated with the other anticoagulant treatment. Rivaroxaban induced a significant prolongation of the prothrombin time (15.8 +/- 1.3 versus 12.3 +/- 0.7 seconds at baseline; P<0.001) that was immediately and completely reversed by PCC (12.8 +/- 1.0; P<0.001). The endogenous thrombin potential was inhibited by rivaroxaban (51 +/- 22%; baseline, 92 +/- 22%; P=0.002) and normalized with PCC (114 +/- 26%; P<0.001), whereas saline had no effect. Dabigatran increased the activated partial thromboplastin time, ecarin clotting time (ECT), and thrombin time. Administration of PCC did not restore these coagulation tests. Conclusion-Prothrombin complex concentrate immediately and completely reverses the anticoagulant effect of rivaroxaban in healthy subjects but has no influence on the anticoagulant action of dabigatran at the PCC dose used in this study.

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