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摘要
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Fondaparinux sodium, a selective factor Xa inhibitor, is the first in a new class of antithrombotics. It binds selectively with high affinity to antithrombin III and specifically catalyses the inactivation of factor Xa. The elimination half-life of fondaparinux sodium permits once daily treatment. A randomised, double-blind, parallel-group, dose-ranging, multicentre phase IIb study in 933 eligible patients established that a subcutaneous dose of between 1.5 and 3mg of fondaparinux sodium has the optimum efficacy and safety profile for prophylaxis of venous thromboembolism in patients undergoing major orthopaedic surgery. Fondaparinux sodium, given to more than 3600 patients undergoing major orthopaedic surgery who participated in prospective, randomised, double-blind, multicentre phase III clinical trials, significantly reduced the incidence of venous thromboembolism, with an overall risk reduction of 55.2% compared with enoxaparin. Fondaparinux sodium was well tolerated by patients undergoing major orthopaedic surgery, and at the recommended clinical dose of 2.5mg has a similar tolerability profile, including bleeding events, to standard enoxaparin regimens. Fondaparinux sodium has not been reported to cause antibody-induced thrombocytopenia.
Keyword:
FACTOR-XA INHIBITOR
HIP-REPLACEMENT SURGERY
RISK-ASSESSMENT MODELS
DEEP-VEIN THROMBOSIS
SYNTHETIC PENTASACCHARIDE
VENOUS THROMBOEMBOLISM
PHARMACOLOGICAL-PROPERTIES
ORTHOPEDIC-SURGERY
ANTITHROMBIN-III
POSTOPERATIVE FONDAPARINUX
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14.4
论文数:
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被引数:
2.3W
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