Phase III Trials of New Oral Anticoagulants in the Acute Treatment and Secondary Prevention of VTE: Comparison and Critique of Study Methodology and Results

被引:33
作者
Cohen, Alexander T. [1 ]
Imfeld, Stephan [2 ,3 ]
Rider, Thomas [4 ]
机构
[1] Guys & St Thomas NHS Fdn Trust, Dept Thrombosis & Haemostasis, London SE1, England
[2] Kings Coll Hosp London, London SE5 9RS, England
[3] Univ Basel Hosp, CH-4031 Basel, Switzerland
[4] Royal Sussex Cty Hosp, Brighton BN2 5BE, E Sussex, England
关键词
Clotting factor inhibitors; Low molecular weight heparin; New oral anticoagulants; Oral anticoagulant; Venous thromboembolism; DEEP-VEIN THROMBOSIS; RECURRENT VENOUS THROMBOEMBOLISM; VITAMIN-K ANTAGONISTS; ED AMERICAN-COLLEGE; PULMONARY-EMBOLISM; ANTITHROMBOTIC THERAPY; DOUBLE-BLIND; WARFARIN; RISK; DABIGATRAN;
D O I
10.1007/s12325-014-0119-7
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The traditional treatment of venous thromboembolism (VTE) has been use of heparin and vitamin K antagonists (VKA), and although shown to be effective, they have numerous limitations. New oral anticoagulants (NOACs) including direct thrombin (factor IIa) inhibitors (dabigatran) and selective factor Xa inhibitors (rivaroxaban, apixaban and edoxaban) have emerged as promising alternatives with the potential to overcome the limitations of traditional treatments. Clinical trials have been performed with a view to making significant changes to the acute, long-term and extended treatment of VTE. Data are now available on the efficacy and safety, including bleeding rates, of the NOACs in comparison with VKA in the acute treatment and secondary prevention of VTE as well as in comparison with placebo extended VTE treatment. This review compares and contrasts the design and results of the Phase III trials of NOACs in VTE and discusses the implications of the NOACs in terms of treatment strategies in VTE patients.
引用
收藏
页码:473 / 493
页数:21
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