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口服因子 Xa 抑制剂用于 ACS 的长期管理。

Oral factor Xa inhibitors for the long-term management of ACS.

机构信息

Division of Cardiology, Duke University Medical Center, Box 3850, 2400 Pratt Street, Durham, NC 27705, USA.

出版信息

Nat Rev Cardiol. 2012 Feb 21;9(7):392-401. doi: 10.1038/nrcardio.2012.18.

Abstract

Despite considerable reductions in cardiovascular events in patients with an acute coronary syndrome (ACS) receiving dual antiplatelet therapy (DAPT), substantial residual risk persists. This unmet need has stimulated the development of anticoagulant drugs that target specific coagulation factors involved in the pathogenesis of thrombosis after atheromatous plaque disruption. Factor Xa is an attractive target for inhibition because of both its integral role in coagulation and its recognized participation in cellular proliferation and inflammation. Several oral, direct factor Xa inhibitors are undergoing investigation and large, phase III clinical trials of two agents, apixaban and rivaroxaban, in patients with an ACS have been completed. On the basis of the known pathobiology of ACS, one might anticipate that drugs in this class of anticoagulant would beneficially reduce ischemic and thrombotic events; however, a strategy of combined anticoagulant therapy and DAPT is likely to increase concomitant bleeding complications. The balance of benefit and risk will ultimately determine uptake in clinical practice. We review the available data on factor Xa inhibitors in the long-term management of patients with an ACS.

摘要

尽管急性冠状动脉综合征 (ACS) 患者接受双联抗血小板治疗 (DAPT) 后心血管事件显著减少,但仍存在大量残余风险。这种未满足的需求刺激了抗凝药物的发展,这些药物针对动脉粥样斑块破裂后血栓形成发病机制中涉及的特定凝血因子。由于因子 Xa 在凝血中的重要作用及其在细胞增殖和炎症中的公认参与,因子 Xa 是抑制的一个有吸引力的靶点。几种口服、直接的因子 Xa 抑制剂正在研究中,两种药物,即阿哌沙班和利伐沙班,在 ACS 患者中的大型 III 期临床试验已经完成。基于 ACS 的已知病理生物学,人们可能预期该类抗凝药物将有益地减少缺血和血栓事件;然而,联合抗凝治疗和 DAPT 的策略可能会增加伴随的出血并发症。最终,获益与风险的平衡将决定其在临床实践中的应用。我们回顾了因子 Xa 抑制剂在 ACS 患者长期管理中的现有数据。

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