Akins Paul T, Feldman Harvey A, Zoble Robert G, Newman David, Spitzer Stefan G, Diener Hans-Christoph, Albers Gregory W
Mercy Stroke Center, Sacramento, CA, USA.
Stroke. 2007 Mar;38(3):874-80. doi: 10.1161/01.STR.0000258004.64840.0b. Epub 2007 Jan 25.
Patients with nonvalvular atrial fibrillation and prior stroke or transient ischemic attack (TIA) are at high risk for recurrent stroke. We investigated whether ximelagatran was noninferior to warfarin in patients with prior stroke or TIA.
We analyzed pooled data from the SPORTIF III and V trials in patients with prior stroke/TIA. The primary outcome was the composite annual rate of both ischemic and hemorrhagic strokes and systemic embolic events. Secondary analyses considered ischemic and hemorrhagic strokes separately, bleeding, and nonrandomized, concomitant therapy with aspirin < or =100 mg/d.
Patients from SPORTIF III (n=3407) and SPORTIF V (n=3922) trials were categorized by prior stroke/TIA (21%) versus no prior stroke/TIA (79%) and by treatment group (ximelagatran vs warfarin). The primary event rate in patients with prior stroke/TIA was 2.83%/y with ximelagatran and 3.27%/y with warfarin (absolute difference, -0.44%; 95% CI, -1.88 to1.01; P=0.625). In those without prior stroke/TIA, the primary event rate was 1.31%/y with ximelagatran and 1.26%/y with warfarin (P=NS). Ischemic strokes outnumbered cerebral hemorrhages with both warfarin (31 of 36) and ximelagatran (30 of 32) treatment (difference between treatments was not significant). Combining aspirin with either anticoagulant was associated with higher rates of major bleeding (1.5%/y with warfarin and 4.95%/y with warfarin plus aspirin, P=0.004; 2.35%/y with ximelagatran and 5.09%/y with ximelagatran plus aspirin, P=0.046) but not lower rates of primary events.
Ximelagatran was at least as effective as well-controlled warfarin for the secondary prevention of stroke. The nonrandomized, concomitant treatment with aspirin and anticoagulation was associated with increased bleeding without evidence of a reduction in primary outcome events.
非瓣膜性心房颤动且既往有卒中或短暂性脑缺血发作(TIA)的患者再次发生卒中的风险很高。我们研究了希美加群在既往有卒中或TIA的患者中是否不劣于华法林。
我们分析了SPORTIF III和V试验中既往有卒中/TIA患者的汇总数据。主要结局是缺血性和出血性卒中和全身性栓塞事件的综合年发生率。次要分析分别考虑缺血性和出血性卒中、出血情况,以及阿司匹林剂量≤100mg/d的非随机伴随治疗情况。
SPORTIF III试验(n = 3407)和SPORTIF V试验(n = 3922)的患者按既往有无卒中/TIA(21% vs 79%)以及治疗组(希美加群与华法林)进行分类。既往有卒中/TIA的患者中,希美加群治疗的主要事件发生率为每年2.83%,华法林治疗为每年3.27%(绝对差异为 -0.44%;95%CI为 -1.88至1.01;P = 0.625)。在无既往卒中/TIA的患者中,希美加群治疗的主要事件发生率为每年1.31%,华法林治疗为每年1.26%(P值无统计学意义)。华法林(36例中的31例)和希美加群(32例中的30例)治疗时,缺血性卒中的数量均多于脑出血(治疗组间差异不显著)。将阿司匹林与任何一种抗凝剂联合使用均与更高的大出血发生率相关(华法林单独使用时为每年1.5%,华法林加阿司匹林时为每年4.95%,P = 0.004;希美加群单独使用时为每年2.35%,希美加群加阿司匹林时为每年5.09%,P = 0.046),但主要事件发生率并未降低。
在卒中二级预防方面,希美加群至少与控制良好的华法林效果相当。阿司匹林与抗凝剂的非随机伴随治疗与出血增加相关,且无证据表明主要结局事件减少。