University of Kent, Canterbury, UK.
Cerebrovasc Dis. 2013;36(1):74-8. doi: 10.1159/000352058. Epub 2013 Jul 30.
The Warfarin versus Aspirin in Reduced Cardiac Ejection Fraction trial found no difference between warfarin and aspirin in patients with low ejection fraction in sinus rhythm for the primary outcome: first to occur of 84 incident ischemic strokes (IIS), 7 intracerebral hemorrhages or 531 deaths. Prespecified secondary analysis showed a 48% hazard ratio reduction (p = 0.005) for warfarin in IIS. Cardioembolism is likely the main pathogenesis of stroke in heart failure. We examined the IIS benefit for warfarin in more detail in post hoc secondary analyses.
We subtyped IIS into definite, possible and noncardioembolic using the Stroke Prevention in Atrial Fibrillation method. Statistical tests, stratified by prior ischemic stroke or transient ischemic attack, were the conditional binomial for independent Poisson variables for rates, the Cochran-Mantel-Haenszel test for stroke subtype and the van Elteren test for modified Rankin Score (mRS) and National Institute of Health Stroke Scale (NIHSS) distributions, and an exact test for proportions.
Twenty-nine of 1,142 warfarin and 55 of 1,163 aspirin patients had IIS. The warfarin IIS rate (0.727/100 patient-years, PY) was lower than for aspirin (1.36/100 PY, p = 0.003). Definite cardioembolic IIS was less frequent on warfarin than aspirin (0.22 vs. 0.55/100 PY, p = 0.012). Possible cardioembolic IIS tended to be less frequent on warfarin than aspirin (0.37 vs. 0.67/100 PY, p = 0.063) but noncardioembolic IIS showed no difference: 5 (0.12/100 PY) versus 6 (0.15/100 PY, p = 0.768). Among patients experiencing IIS, there were no differences by treatment arm in fatal IIS, baseline mRS, mRS 90 days after IIS, and change from baseline to post-IIS mRS. The warfarin arm showed a trend to a lower proportion of severe nonfatal IIS [mRS 3-5; 3/23 (13.0%) vs. 16/48 (33.3%), p = 0.086]. There was no difference in NIHSS at the time of stroke (p = 0.825) or in post-IIS mRS (p = 0.948) between cardioembolic, possible cardioembolic and noncardioembolic stroke including both warfarin and aspirin groups.
The observed benefits in the reduction of IIS for warfarin compared to aspirin are most significant for cardioembolic IIS among patients with low ejection fraction in sinus rhythm. This is supported by trends to lower frequencies of severe IIS and possible cardioembolic IIS in patients on warfarin compared to aspirin.
华法林与窦性心律低射血分数患者的阿司匹林试验发现,在主要结局(首次发生 84 例缺血性脑卒中[IIS]、7 例颅内出血或 531 例死亡)方面,华法林与阿司匹林之间无差异。预先设定的次要分析显示,华法林治疗 IIS 的风险比降低了 48%(p = 0.005)。在心力衰竭患者中,心源性栓塞可能是脑卒中的主要发病机制。我们在事后的次要分析中更详细地检查了华法林在 IIS 中的获益。
我们使用房颤卒中预防方法将 IIS 分为明确、可能和非心源性栓塞。统计学检验按既往缺血性卒中和短暂性脑缺血发作分层,用于独立泊松变量的条件二项式用于率, Cochran-Mantel-Haenszel 检验用于脑卒中亚型,van Elteren 检验用于改良 Rankin 评分(mRS)和 NIH 卒中量表(NIHSS)分布,以及确切概率检验用于比例。
华法林组 1142 例患者中有 29 例,阿司匹林组 1163 例患者中有 55 例发生 IIS。华法林组 IIS 发生率(0.727/100 患者年,PY)低于阿司匹林组(1.36/100 PY,p = 0.003)。华法林组明确的心源性栓塞性 IIS 发生率低于阿司匹林组(0.22 比 0.55/100 PY,p = 0.012)。华法林组可能的心源性栓塞性 IIS 发生率也低于阿司匹林组(0.37 比 0.67/100 PY,p = 0.063),而非心源性栓塞性 IIS 无差异:5 例(0.12/100 PY)与 6 例(0.15/100 PY,p = 0.768)。在发生 IIS 的患者中,治疗组之间在 IIS 致死率、基线 mRS、IIS 后 90 天 mRS、基线至 IIS 后 mRS 的变化方面无差异。华法林组严重非致死性 IIS 的比例较低[改良 Rankin 评分 3-5;3/23(13.0%)比 16/48(33.3%),p = 0.086],趋势更明显。在卒中时 NIHSS 或 IIS 后 mRS 方面,华法林和阿司匹林组的心源性、可能的心源性和非心源性卒中之间无差异(p = 0.825 和 p = 0.948)。
与阿司匹林相比,华法林降低 IIS 的观察到的益处在窦性心律低射血分数患者中的心源性栓塞性 IIS 中最为显著。这一结果得到了华法林组较阿司匹林组 IIS 严重程度较低和可能的心源性栓塞性 IIS 发生率较低的趋势支持。