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抗凝治疗的最新进展:口服直接凝血酶和 Xa 因子抑制剂。

Recent progress in anticoagulant therapy: oral direct inhibitors of thrombin and factor Xa.

机构信息

VA Boston Healthcare System and Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.

出版信息

J Thromb Haemost. 2011 Jul;9 Suppl 1:12-9. doi: 10.1111/j.1538-7836.2011.04321.x.

Abstract

While parenteral anticoagulants such as unfractionated and low molecular weight heparins and the oral vitamin K antagonists are effective for the prevention and treatment of thrombosis, they have a number of limitations. Up until recently, vitamin K antagonists (e.g. warfarin) have been the only available oral anticoagulants. These drugs have a delayed onset of action, food and drug interactions, and variable pharmacokinetics/pharmacodynamics such that regular laboratory monitoring and dose adjustments are required to maintain the International Normalized Ratio (INR) in the therapeutic range. New oral anticoagulants that selectively inhibit either thrombin (dabigatran etexilate) or factor Xa (rivaroxaban, apixaban) have now gained approval in many countries for some clinical indications. Unlike warfarin, these drugs have a rapid onset of action and a relatively wide therapeutic range such that coagulation monitoring is not required. These agents are more convenient for patients and health care providers, but also have potential for improving clinical outcomes and being more cost-effective than existing agents. This will result in major changes in the way that thrombosis is managed, both with respect to prevention and treatment. The new oral inhibitors of thrombin and factor Xa, however, have limitations and the absence of a need for regular laboratory monitoring makes medication compliance extremely important for maintaining efficacy given their relatively short half-lives. Furthermore there will be challenges in managing patients on these agents who develop recurrent thrombosis or major bleeding until methods to monitor and assess the levels of the new agents are readily available and specific antidotes are developed.

摘要

虽然普通肝素、低分子肝素和口服维生素 K 拮抗剂等肠外抗凝剂可有效预防和治疗血栓形成,但它们存在许多局限性。直到最近,维生素 K 拮抗剂(如华法林)一直是唯一可用的口服抗凝剂。这些药物起效时间延迟,存在食物和药物相互作用,药代动力学/药效学也存在差异,因此需要定期进行实验室监测和剂量调整,以维持国际标准化比值(INR)在治疗范围内。新型口服抗凝剂,选择性抑制凝血酶(达比加群酯)或因子 Xa(利伐沙班、阿哌沙班),现已在许多国家获得批准,可用于一些临床适应证。与华法林不同,这些药物起效迅速,治疗窗较宽,因此无需进行凝血监测。这些药物对患者和医疗保健提供者更为方便,但也有可能改善临床结局,并比现有药物更具成本效益。这将导致血栓管理方式发生重大变化,无论是在预防还是治疗方面。然而,新型口服凝血酶和因子 Xa 抑制剂存在局限性,由于半衰期相对较短,因此无需定期进行实验室监测,这使得保持药物疗效的用药依从性极为重要。此外,在这些药物的管理方面还存在挑战,例如需要监测和评估新药物水平,直到这些方法和特定的解毒剂变得易于获得。

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