Coleman Craig I, Haas Sylvia, Turpie Alexander G G, Kuhls Silvia, Hess Susanne, Evers Thomas, Amarenco Pierre, Kirchhof Paulus, Camm A John
Department of Pharmacy Practice, University of Connecticut School of Pharmacy, Storrs, Connecticut.
Vascular Center, Munich, Germany.
Clin Cardiol. 2016 Oct;39(10):565-569. doi: 10.1002/clc.22565. Epub 2016 Jun 30.
The efficacy, safety, and ease of use of rivaroxaban may reduce anticoagulation-treatment burden and improve nonvalvular atrial fibrillation (NVAF) patient satisfaction compared with vitamin K antagonists (VKAs).
Transitioning from a VKA to rivaroxaban improves treatment satisfaction in routine practice.
Xarelto for Prevention of Stroke in Patients With Atrial Fibrillation (XANTUS) is a prospective, noninterventional study in patients with NVAF prescribed rivaroxaban for prevention of stroke in routine practice. Patients receiving a VKA 4 weeks prior to the initial XANTUS study visit and switched to rivaroxaban were asked to complete the Anti-Clot Treatment Scale (ACTS). Changes from the initial visit to the first follow-up visit at ∼ 3 months (corresponding to a comparison of rivaroxaban vs prior VKA) for ACTS burden and benefit scores were calculated using and reported as least squared mean differences (LSMDs) with 95% confidence intervals (CIs).
The study included 1291 NVAF patients with prior VKA treatment. The mean baseline ACTS burden and benefit scores were 50.51 ± 8.42 and 10.30 ± 2.70, respectively. After ∼ 3 months of rivaroxaban treatment, LSMDs were 4.38 points (95% CI: 2.53-6.22, P < 0.0001) for the burden and 1.01 points (95% CI: 0.27-1.75, P = 0.0075) for the benefit score. Fifty-four percent and 48% of patients reported experiencing at least a minimally important clinical difference in burden and benefit scores, respectively.
Within this XANTUS cohort, switching from a VKA to rivaroxaban yielded statistically and clinically significant improvements in ACT burden and benefit scores.
与维生素K拮抗剂(VKA)相比,利伐沙班的疗效、安全性及易用性可能会减轻抗凝治疗负担并提高非瓣膜性心房颤动(NVAF)患者的满意度。
在常规实践中,从VKA转换为利伐沙班可提高治疗满意度。
利伐沙班预防心房颤动患者卒中(XANTUS)研究是一项针对在常规实践中使用利伐沙班预防卒中的NVAF患者的前瞻性非干预性研究。在XANTUS研究首次访视前4周接受VKA治疗且转换为利伐沙班的患者被要求完成抗凝治疗量表(ACTS)。计算并报告从首次访视到约3个月时首次随访访视(对应利伐沙班与先前VKA的比较)ACTS负担和获益评分的变化,以最小二乘均数差值(LSMDs)及95%置信区间(CIs)表示。
该研究纳入了1291例曾接受VKA治疗的NVAF患者。ACTS负担和获益评分的平均基线分别为50.51±8.42和10.30±2.70。利伐沙班治疗约3个月后,负担评分的LSMDs为4.38分(95%CI:2.53 - 6.22,P < 0.0001),获益评分为1.01分(95%CI:0.27 - 1.75,P = 0.0075)。分别有54%和48%的患者报告在负担和获益评分上至少有最小重要临床差异。
在这个XANTUS队列中,从VKA转换为利伐沙班在ACTS负担和获益评分方面产生了具有统计学意义和临床意义的改善。