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Recent advances in the management of venous thromboembolism

机译:静脉血栓栓塞治疗的最新进展

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摘要

Venous thromboembolism (VTE) is a spectrum of diseases that includes deep vein thrombosis (DVT) and pulmonary embolism (PE). Anticoagulant treatment is the mainstay of therapy for VTE. Unfractionated heparin (UFH) or low molecular weight heparin (LMWH) followed by vitamin K antagonists have been the treatment of choice for most patients with VTE, with the aim to prevent thrombus extension or embolization and recurrent VTE. Fondaparinux, a selective, indirect, parenteral factor Xa inhibitor, is now also approved for the initial treatment of VTE and represents an important alternative to UFH or LMWH. Secondary prevention of VTE with vitamin K antagonists is usually prescribed for a minimum of three months, with the duration of treatment based on the presence or absence of major identifiable risk factors for the index event. Patients with permanent risk factors or patients with recurrent DVT or PE require life long secondary prevention. Over the last years, new oral anticoagulant agents have been developed and are now undergoing extensive clinical evaluation in several settings, including the treatment of VTE. New oral anticoagulants include selective, direct thrombin inhibitors, such as dabigatran etexilate, and selective, direct factor Xa inhibitos, such as rivaroxaban, apixaban or edoxaban. All these drugs are admistered at fixed daily doses and do not require laboratory monitoring. The positive results of the first completed clinical trials suggest that a new era in the management of VTE is about to begin.
机译:静脉血栓栓塞症(VTE)是一系列疾病,包括深静脉血栓形成(DVT)和肺栓塞(PE)。抗凝治疗是VTE治疗的主要手段。对于大多数VTE患者,未分级肝素(UFH)或低分子量肝素(LMWH)继之以维生素K拮抗剂已成为大多数VTE患者的治疗选择,目的是防止血栓扩展或栓塞和VTE复发。 Fondaparinux是一种选择性的,间接的肠胃外Xa抑制剂,现在也被批准用于VTE的初始治疗,它是UFH或LMWH的重要替代品。通常建议使用维生素K拮抗剂对VTE进行二级预防,至少持续三个月,治疗的持续时间取决于是否存在指数事件的主要可识别危险因素。具有永久危险因素的患者或复发性DVT或PE的患者需要终生二级预防。在过去的几年中,已经开发了新的口服抗凝剂,并且目前正在包括VTE治疗在内的多种环境中进行广泛的临床评估。新的口服抗凝剂包括选择性的直接凝血酶抑制剂(例如达比加群酯)和选择性的直接因子Xa抑制剂(例如利伐沙班,阿哌沙班或依多沙班)。所有这些药物均以固定的每日剂量服用,不需要实验室监控。首次完成的临床试验的积极结果表明,VTE管理的新时代即将开始。

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