Turan Tanya N, Maidan Lucian, Cotsonis George, Lynn Michael J, Romano Jose G, Levine Steven R, Chimowitz Marc I
Medical University of South Carolina, Charleston, SC, USA.
Stroke. 2009 Feb;40(2):505-9. doi: 10.1161/STROKEAHA.108.528281. Epub 2008 Dec 18.
We sought to determine if patients with intracranial stenosis who have a transient ischemic attack or stroke on antithrombotic therapy are at particularly high risk for recurrent stroke.
We compared baseline features and the rates of stroke or vascular death and stroke in the territory of the symptomatic artery between patients ON (n=299) versus OFF (n=269) antithrombotics at the time of their qualifying event for the Warfarin-Aspirin Symptomatic Intracranial Disease (WASID) trial.
In univariate analyses, there was no difference in the rates of stroke or vascular death (21% versus 23%; hazard ratio [ON/OFF], 0.91; 95% CI, 0.64 to 1.29; P=0.59) or stroke in territory (13% versus 14%; hazard ratio [ON/OFF], 0.90; 95% CI, 0.57 to 1.39; P=0.61) between patients ON versus OFF antithrombotics at the time of their qualifying event. A multivariable analysis adjusted for the difference in risk factors between patients ON and OFF antithrombotic therapy also showed no significant differences in the combined end point of stroke or vascular death (hazard ratio [ON/OFF], 0.86; 95% CI, 0.55 to 1.34; P=0.51) or stroke in territory (hazard ratio [ON/OFF], 1.01; 95% CI, 0.58 to 1.77; P=0.97) between patients ON versus OFF antithrombotic therapy at the time of the qualifying event.
Patients with intracranial stenosis who fail antithrombotic therapy are not at higher risk of stroke than those who do not fail antithrombotic therapy. Given our finding that patients ON and OFF antithrombotic therapy are both at high risk for stroke in the territory, intracranial stenting trials should not be limited to just those who fail antithrombotic therapy.
我们试图确定接受抗栓治疗时发生短暂性脑缺血发作或卒中的颅内狭窄患者是否具有特别高的复发性卒中风险。
我们比较了华法林-阿司匹林有症状颅内疾病(WASID)试验合格事件发生时正在接受(n = 299)与未接受(n = 269)抗栓治疗的患者的基线特征、卒中或血管性死亡发生率以及症状性动脉供血区的卒中发生率。
在单因素分析中,正在接受与未接受抗栓治疗的患者在合格事件发生时,其卒中或血管性死亡发生率(21% 对 23%;风险比[正在接受/未接受],0.91;95%可信区间,0.64至1.29;P = 0.59)或供血区卒中发生率(13% 对 14%;风险比[正在接受/未接受],0.90;95%可信区间,0.57至1.39;P = 0.61)无差异。对正在接受与未接受抗栓治疗患者之间的危险因素差异进行校正的多变量分析也显示,在合格事件发生时,正在接受与未接受抗栓治疗的患者在卒中或血管性死亡联合终点(风险比[正在接受/未接受],0.86;95%可信区间,0.55至1.34;P = 0.51)或供血区卒中(风险比[正在接受/未接受],1.01;95%可信区间,0.58至1.77;P = 0.