Deitelzweig Steven, Luo Xuemei, Gupta Kiran, Trocio Jeffrey, Mardekian Jack, Curtice Tammy, Lingohr-Smith Melissa, Menges Brandy, Lin Jay
a Ochsner Clinic Foundation , Department of Hospital Medicine and The University of Queensland School of Medicine , Ochsner Clinical School , New Orleans , LA , USA.
b Pfizer Inc. , New York , NY , USA.
Curr Med Res Opin. 2017 Oct;33(10):1745-1754. doi: 10.1080/03007995.2017.1334638. Epub 2017 Aug 29.
To compare the risk of stroke/systemic embolism (S/SE) and major bleeding (MB) of elderly (≥65 years of age) nonvalvular atrial fibrillation (NVAF) patients initiating apixaban vs. rivaroxaban, dabigatran, or warfarin.
NVAF patients with Medicare Advantage coverage in the US initiating oral anticoagulants (OACs, index event) were identified from the Humana database (1 January 2013-30 September 2015) and grouped into cohorts depending on OAC initiated. Propensity score matching (PSM), 1:1, was conducted among patients treated with apixaban vs. each other OAC, separately. Rates of S/SE and MB were evaluated in the follow-up. Cox regressions were used to compare the risk of S/SE and MB between apixaban and each of the other OACs during the follow-up.
The matched pairs of apixaban vs. rivaroxaban (n = 13,620), apixaban vs. dabigatran (n = 4654), and apixaban vs. warfarin (n = 14,214) were well balanced for key patient characteristics. Adjusted risks for S/SE (hazard ratio [HR] vs. rivaroxaban: 0.72, p = .003; vs. warfarin: 0.65, p < .001) and MB (HR vs. rivaroxaban: 0.49, p < .001; vs. warfarin: 0.53, p < .001) were significantly lower during the follow-up for patients treated with apixaban vs. rivaroxaban and warfarin. Adjusted risks for S/SE (HR: 0.78, p = .27) and MB (HR: 0.82, p = .23) of NVAF patients treated with apixaban vs. dabigatran trended to be lower, but did not reach statistical significance.
In the real-world setting after controlling for differences in patient characteristics, apixaban is associated with significantly lower risk of S/SE and MB than rivaroxaban and warfarin, and a trend towards better outcomes vs. dabigatran among elderly NVAF patients in the US.
比较开始使用阿哌沙班与利伐沙班、达比加群或华法林的老年(≥65岁)非瓣膜性心房颤动(NVAF)患者发生卒中/全身性栓塞(S/SE)和大出血(MB)的风险。
从Humana数据库(2013年1月1日至2015年9月30日)中识别出在美国参加医疗保险优势计划且开始口服抗凝剂(OACs,索引事件)的NVAF患者,并根据开始使用的OAC将其分组。在接受阿哌沙班治疗的患者与其他每种OAC治疗的患者之间分别进行1:1倾向评分匹配(PSM)。在随访中评估S/SE和MB的发生率。使用Cox回归比较随访期间阿哌沙班与其他每种OAC之间S/SE和MB的风险。
阿哌沙班与利伐沙班(n = 13,620)、阿哌沙班与达比加群(n = 4654)以及阿哌沙班与华法林(n = 14,214)的匹配对在关键患者特征方面具有良好的平衡性。与利伐沙班相比,阿哌沙班治疗的患者在随访期间S/SE的调整风险(风险比[HR]:0.72,p = 0.003;与华法林相比:0.65,p < 0.001)和MB的调整风险(HR与利伐沙班相比:0.49,p < 0.001;与华法林相比:0.53,p < 0.001)显著更低。与达比加群相比,阿哌沙班治疗的NVAF患者S/SE(HR:0.78,p = 0.27)和MB(HR:0.82,p = 0.23)的调整风险有降低趋势,但未达到统计学显著性。
在控制患者特征差异后的真实世界环境中,在美国老年NVAF患者中,阿哌沙班与S/SE和MB的风险显著低于利伐沙班和华法林相关,并且与达比加群相比有更好结局的趋势。