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首页> 外文期刊>Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis >Patient-reported treatment satisfaction with oral rivaroxaban versus standard therapy in the treatment of acute symptomatic deep-vein thrombosis
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Patient-reported treatment satisfaction with oral rivaroxaban versus standard therapy in the treatment of acute symptomatic deep-vein thrombosis

机译:患者报告的口服利伐沙班与标准疗法对急性症状性深静脉血栓形成的治疗满意度

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Rivaroxaban, an oral, direct factor Xa inhibitor, has been approved for the treatment of deep-vein thrombosis (DVT) and pulmonary embolism (PE) and the prevention of recurrent DVT and PE as a fixed-dose, single-drug regimen that does not require initial heparinisation, routine coagulation monitoring or dose adjustment. This study evaluated patient-reported treatment satisfaction in EINSTEIN DVT - a large, open-label, randomised study that compared rivaroxaban with enoxaparin/ vitamin K antagonist (VKA) therapy in patients with acute symptomatic DVT without PE. As part of EINSTEIN DVT, a total of 1,472 patients in seven countries were asked to complete a new, validated measure of treatment satisfaction - the Anti-Clot Treatment Scale (ACTS) - at scheduled visits throughout 12 months of treatment. ACTS scores were compared between study groups in the intentionto-treat population. Patients reported greater satisfaction in the rivaroxaban group compared with the enoxaparin/VKA group, with higher mean ACTS scores across visits. Mean ACTS Burdens scores were 55.2 vs 52.6 (p<0.0001) in favour of rivaroxaban, equivalent to a moderate effect size of 0.42. The treatment effect was consistent over time, with the mean score difference ranging from 2.18 (month 2) to 3.18 (month 12). Overall mean ACTS Benefits scores were 11.7 vs 11.5 in favour of rivaroxaban (p=0.006). This was associated with a small overall effect size of 0.12. The improvement in ACTS Benefits for rivaroxaban became apparent at month 2 and subsequent visits. Rivaroxaban results in improved treatment satisfaction compared with enoxaparin/VKA among patients with DVT, particularly in reducing patient-reported anticoagulation burden.
机译:利伐沙班是口服,直接因子Xa抑制剂,已被批准用于治疗深静脉血栓形成(DVT)和肺栓塞(PE)以及预防DVT和PE复发,作为固定剂量,单药治疗的方法不需要初始肝素化,常规凝血监测或剂量调整。这项研究评估了患者报告的EINSTEIN DVT的治疗满意度-一项大型,开放标签,随机研究,比较了利伐沙班与依诺肝素/维生素K拮抗剂(VKA)治疗无PE的急性症状性DVT患者。作为EINSTEIN DVT的一部分,在整个治疗12个月的定期拜访中,要求七个国家的1,472名患者完成一项新的,经过验证的有效治疗满意度测度-抗凝治疗量表(ACTS)。在意向性治疗人群的研究组之间比较了ACTS得分。与依诺肝素/ VKA组相比,利伐沙班组患者的满意度更高,各次访视的平均ACTS评分更高。利伐沙班的平均ACTS Burdens评分为55.2 vs 52.6(p <0.0001),相当于中度效应值为0.42。随着时间的推移,治疗效果是一致的,平均评分差异为2.18(第2个月)至3.18(第12个月)。利伐沙班的总体平均ACTS收益评分为11.7 vs 11.5(p = 0.006)。这与0.12的较小总体效果大小有关。在第2个月及以后的随访中,利伐沙班的ACTS益处有所改善。与依诺肝素/ VKA相比,利伐沙班可使DVT患者的治疗满意度得到改善,尤其是减少了患者报告的抗凝负担。

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