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我如何治疗靶向特异性口服抗凝剂相关出血。

How I treat target-specific oral anticoagulant-associated bleeding.

机构信息

Division of Hematology and Thromboembolism, Department of Medicine, McMaster University, Hamilton, ON, Canada; and.

出版信息

Blood. 2014 Feb 20;123(8):1152-8. doi: 10.1182/blood-2013-09-529784. Epub 2014 Jan 2.

Abstract

Target-specific oral anticoagulants (TSOACs) that directly inhibit thrombin (dabigatran) or factor Xa (rivaroxaban, apixaban) are effective and safe alternatives to vitamin K antagonists (VKAs) and low-molecular-weight heparin (LMWH). Although these agents have practical advantages compared with VKAs and LMWH, there are no antidotes that reverse their anticoagulant effect. Clinical evidence for the efficacy of nonspecific therapies that promote formation of fibrin (prothrombin complex concentrate [PCC], activated PCC [aPCC], and recombinant factor VIIa) in the setting of TSOAC-associated bleeding is lacking, and these prohemostatic products are associated with a risk of thrombosis. In the absence of specific antidotes, addition of PCC or aPCC to maximum supportive therapy may be reasonable for patients with severe or life-threatening TSOAC-associated bleeding. Targeted antidotes for these agents are in development.

摘要

靶向特异性口服抗凝剂(TSOAC)直接抑制凝血酶(达比加群)或因子 Xa(利伐沙班、阿哌沙班),是维生素 K 拮抗剂(VKA)和低分子肝素(LMWH)的有效且安全的替代药物。虽然与 VKA 和 LMWH 相比,这些药物具有实际优势,但没有逆转其抗凝作用的解毒剂。在 TSOAC 相关出血的情况下,促进纤维蛋白形成的非特异性治疗方法(凝血酶原复合物浓缩物[PCC]、活化 PCC[aPCC]和重组因子 VIIa)的疗效的临床证据不足,这些促凝产品与血栓形成的风险相关。在没有特异性解毒剂的情况下,对于严重或危及生命的 TSOAC 相关出血的患者,在最大支持治疗的基础上添加 PCC 或 aPCC 可能是合理的。这些药物的靶向解毒剂正在开发中。

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