Bengtson Lindsay G S, Lutsey Pamela L, Chen Lin Y, MacLehose Richard F, Alonso Alvaro
Health Economics and Outcomes Research, Life Sciences, Optum, Eden Prairie, MN, USA.
Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, MN, USA.
J Cardiol. 2017 Jun;69(6):868-876. doi: 10.1016/j.jjcc.2016.08.010. Epub 2016 Nov 23.
Effectiveness data on novel oral anticoagulants (NOACs) versus warfarin for stroke prevention in non-valvular atrial fibrillation (NVAF) by prior warfarin use are limited.
We used data from the US MarketScan databases from 2009 to 2012. NVAF patients initiating dabigatran or rivaroxaban were matched with up to 5 warfarin users. Propensity score-adjusted Cox regression was used to calculate hazard ratios (HR) and 95% confidence intervals (95% CI) for relevant endpoints in NOACs versus warfarin users. Separate analyses were conducted to compare anticoagulant-naïve users of NOACs and those switching from warfarin.
Among 32,918 dabigatran, 3301 rivaroxaban, and 109,447 warfarin users with NVAF, 225 intracranial bleeds, 1035 ischemic strokes, 958 myocardial infarctions, and 1842 gastrointestinal bleeds were identified. Compared to warfarin users, patients initiating NOACs had similar ischemic stroke rates and lower intracranial bleeding rates, while the gastrointestinal bleeding rate was higher in dabigatran users than warfarin users. Associations of dabigatran with ischemic stroke risk differed between anticoagulant-naïve initiators and patients switching from warfarin; dabigatran was associated with lower ischemic stroke rates in naïve users (HR 0.65, 95% CI 0.52-0.82) but not in switchers (HR 1.20, 95% CI 0.95-1.51), compared to warfarin. Risk of stroke and bleeding was not different between rivaroxaban and warfarin users.
Real-world effectiveness of NOACs (compared to warfarin) for diverse outcomes was comparable to efficacy reported in published clinical trials. However, harms and benefits of switching from warfarin to dabigatran need to be evaluated.
新型口服抗凝药(NOACs)与华法林相比,在既往使用华法林的非瓣膜性心房颤动(NVAF)患者中预防卒中的有效性数据有限。
我们使用了2009年至2012年美国市场扫描数据库的数据。启动达比加群或利伐沙班的NVAF患者与多达5名华法林使用者进行匹配。倾向评分调整的Cox回归用于计算NOACs使用者与华法林使用者相关终点的风险比(HR)和95%置信区间(95%CI)。进行了单独分析,以比较未使用过抗凝剂的NOACs使用者和从华法林转换过来的使用者。
在32918名使用达比加群、3301名使用利伐沙班和109447名使用华法林的NVAF患者中,发现了225例颅内出血、1035例缺血性卒中、958例心肌梗死和1842例胃肠道出血。与华法林使用者相比,启动NOACs的患者缺血性卒中发生率相似,颅内出血率较低,而达比加群使用者的胃肠道出血率高于华法林使用者。未使用过抗凝剂的启动者和从华法林转换过来的患者中,达比加群与缺血性卒中风险的关联不同;与华法林相比,达比加群在未使用过抗凝剂的使用者中缺血性卒中发生率较低(HR 0.65,95%CI 0.52 - 0.82),但在转换者中并非如此(HR 1.20,95%CI 0.95 - 1.51)。利伐沙班使用者和华法林使用者之间的卒中和出血风险没有差异。
NOACs(与华法林相比)在实际应用中对各种结局的有效性与已发表临床试验中报道的疗效相当。然而,需要评估从华法林转换到达比加群的利弊。