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新型靶向特异性口服抗凝药物的药理学。

Pharmacology of the new target-specific oral anticoagulants.

机构信息

Department Pharmacy Practice, Albany College of Pharmacy and Health Sciences, 106 New Scotland Ave., Albany, NY 12208, USA.

出版信息

J Thromb Thrombolysis. 2013 Aug;36(2):133-40. doi: 10.1007/s11239-013-0929-5.

Abstract

Oral anticoagulation therapy is transforming with the advent of the target specific oral anticoagulants, particularly, the direct thrombin inhibitors and factor Xa inhibitors. These agents have demonstrated clinical efficacy and safety and offer several potential advantages over current standard of care therapy, warfarin. Nevertheless, the pharmacology between the newly approved oral anticoagulants differs and must be considered for appropriate management and patient selection. The pharmacodynamics and pharmacokinetics of dabigatran etexilate, rivaroxaban, apixaban and edoxaban are discussed in detail, which may translate into considerable clinical implications.

摘要

口服抗凝治疗随着靶向特定的口服抗凝剂的出现而发生转变,特别是直接凝血酶抑制剂和因子 Xa 抑制剂。这些药物已显示出临床疗效和安全性,并为当前的标准治疗方法(华法林)提供了几个潜在的优势。然而,新批准的口服抗凝剂之间的药理学差异必须加以考虑,以便进行适当的管理和患者选择。达比加群酯、利伐沙班、阿哌沙班和依度沙班的药效学和药代动力学进行了详细讨论,这可能会转化为重要的临床意义。

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