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Direct oral anticoagulants for extended treatment of venous thromboembolism: insights from the EINSTEIN CHOICE study

机译:直接口服抗凝剂扩展治疗静脉血栓栓塞症:EINSTEIN CHOICE研究的真知灼见

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摘要

The risk of recurrence of venous thromboembolism (VTE) persists after interruption of the initial anticoagulation therapy. New evidence shows that direct oral anticoagulants are effective for extended treatment of VTE and may reduce the risk of all-cause mortality. The optimal duration of anticoagulation after VTE is, however, controversial and complicated by the need for individualised assessment and balance between thrombosis and bleeding risks. Three direct oral anticoagulants (rivaroxaban, apixaban and dabigatran) have been studied for extended treatment of VTE. Dabigatran was shown to be safer than vitamin K antagonists and similarly effective for the prevention of recurrent VTE. Dabigatran, apixaban and rivaroxaban resulted in significant decreases in the rate of recurrent symptomatic VTE when compared to placebo, without a statistically significant difference in the risk of major bleeding. The latest guidelines of the American College of Chest Physicians suggest the use of low-dose aspirin to prevent VTE recurrence in patients who want to stop anticoagulation. In the randomised, double-blind, phase 3 EINSTEIN CHOICE trial, once-daily rivaroxaban at doses of 20 mg or 10 mg and 100 mg of aspirin were compared in VTE patients for whom there was clinical equipoise for extended anticoagulation. Either a treatment dose (20 mg) or a prophylactic dose (10 mg) of rivaroxaban significantly reduced the risk of VTE recurrence without a significant increase in bleeding risk compared with aspirin. The EINSTEIN CHOICE trial included patients with provoked or unprovoked VTE. Patients with VTE provoked by minor persistent or minor transient risk factors enrolled in this trial had not-negligible VTE recurrence rates. These new findings on extended therapy suggest the possibility of anticoagulation regimens at intensities tailored to the patients’ risk profiles and VTE characteristics, with a shift of the risk-benefit balance in favour of extended treatment.
机译:初始抗凝治疗中断后,静脉血栓栓塞(VTE)复发的风险仍然存在。新证据表明,直接口服抗凝剂可有效延长VTE的治疗时间,并可降低全因死亡率的风险。但是,由于需要进行个体化评估以及在血栓形成和出血风险之间取得平衡,VTE后抗凝的最佳持续时间一直存在争议和复杂化。已经研究了三种直接口服抗凝药(利伐沙班,阿哌沙班和达比加群)对VTE的扩展治疗。已显示达比加群比维生素K拮抗剂更安全,并且在预防VTE复发方面同样有效。与安慰剂相比,达比加群,阿哌沙班和利伐沙班导致症状性VTE的复发率显着降低,而发生大出血的风险无统计学差异。美国胸科医师学院的最新指南建议使用小剂量阿司匹林预防想要停止抗凝治疗的患者的VTE复发。在随机,双盲,3期EINSTEIN CHOICE试验中,比较了具有临床抗衡长期抗凝作用的VTE患者每天一次一次利伐沙班的剂量为20 mg或10 mg和阿司匹林。与阿司匹林相比,利伐沙班的治疗剂量(20 mg)或预防剂量(10 mg)均显着降低了VTE复发的风险,而出血风险没有显着增加。 EINSTEIN CHOICE试验纳入了诱发或未诱发VTE的患者。该试验中,由轻微持续性或短暂性短暂危险因素引起的VTE患者的VTE复发率不可忽略。这些有关延长治疗的新发现表明,有可能根据患者的风险状况和VTE特征调整强度的抗凝治疗方案,而风险与收益之间的平衡会转向延长治疗。

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