Emerging anticoagulants for the treatment of venous thromboembolism

被引:82
作者
Weitz, Jeffrey I.
机构
[1] Henderson Res Ctr, Hamilton, ON L8V 1C3, Canada
[2] McMaster Univ, Dept Med, Hamilton, ON L8S 4L8, Canada
[3] McMaster Univ, Dept Biochem & Med Sci, Hamilton, ON L8S 4L8, Canada
关键词
coagulation inhibitors; heparins/glycosaminoglycans; pulmonary embolism; deep vein thrombosis;
D O I
10.1160/TH06-05-0234
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Anticoagulant therapy is the cornerstone of treatment of venous thromboembolism (VTE). Such treatment is divided into two stages. Rapid initial anticoagulation is given to minimize the risk of thrombus extension and fatal pulmonary embolism, whereas extended anticoagulation is aimed at preventing recurrentVTE, thereby reducing the risk of postphlebitic syndrome. With currently available drugs, immediate anticoagulation can only be achieved with parenteral agents, such as heparin, low-molecular-weight heparin, or fondaparinux. Extended treatment usually involves the administration of vitamin K antagonists, such as warfarin. Emerging anticoagulants have the potential to streamline VTE treatment. These agents include idraparinux, a long-acting synthetic pentasaccharide that is given subcutaneously on a once-weekly basis, and new oral anticoagulants that target thrombin or factor Xa. This paper i) reviews the pharmacology of these agents, ii) outlines their potential strengths and weaknesses, iii) describes the results of clinical trials with these new drugs, and iv) identifies the evolving role of new anticoagulants in the management of VTE.
引用
收藏
页码:274 / 284
页数:11
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