Department of Neurosciences, Stroke Center, Medical University of South Carolina, Charleston, USA.
J Stroke Cerebrovasc Dis. 2011 Jul-Aug;20(4):357-68. doi: 10.1016/j.jstrokecerebrovasdis.2011.05.001.
Patients with recent transient ischemic attack (TIA) or stroke caused by 70% to 99% stenosis of a major intracranial artery are at high risk of recurrent stroke on usual medical management, suggesting the need for alternative therapies for this disease.
The Stenting and Aggressive Medical Management for Preventing Recurrent stroke in Intracranial Stenosis trial is an ongoing, randomized, multicenter, 2-arm trial that will determine whether intracranial angioplasty and stenting adds benefit to aggressive medical management alone for preventing the primary endpoint (any stroke or death within 30 days after enrollment or after any revascularization procedure of the qualifying lesion during follow-up, or stroke in the territory of the symptomatic intracranial artery beyond 30 days) during a mean follow-up of 2 years in patients with recent TIA or stroke caused by 70% to 99% stenosis of a major intracranial artery. Aggressive medical management in both arms consists of aspirin 325 mg per day, clopidogrel 75 mg per day for 90 days after enrollment, intensive risk factor management primarily targeting systolic blood pressure <140 mm Hg (<130 mm Hg in diabetics) and low density cholesterol <70 mg/dL, and a lifestyle modification program. The sample size required to detect a 35% reduction in the rate of the primary endpoint from angioplasty and stenting based on the log-rank test with an alpha of 0.05, 80% power, and adjusting for a 2% loss to follow-up and 5% crossover from the medical to the stenting arm is 382 patients per group.
Enrollment began in November 2008 and 451 patients have been enrolled as of March 31, 2011.
This is the first randomized stroke prevention trial to compare angioplasty and stenting with medical therapy in patients with intracranial arterial stenosis and to incorporate intensive management of multiple risk factors and a lifestyle modification program in the study design. Hopefully, the results of the trial will lead to more effective therapy for this high-risk disease.
近期短暂性脑缺血发作(TIA)或由颅内大血管 70%至 99%狭窄引起的卒中患者,在常规药物治疗下,卒中复发风险较高,提示需要为该疾病提供替代疗法。
颅内动脉狭窄血管成形术和强化药物治疗预防卒中复发试验是一项正在进行的、随机、多中心、双臂试验,旨在确定颅内血管成形术和支架置入是否优于强化药物治疗单独用于预防主要终点(任何卒中和入组后 30 天内死亡,或在随访期间符合条件的病变血管再通后 30 天内卒中,或症状性颅内动脉供血区 30 天后的卒中)。平均随访 2 年,入组患者为近期 TIA 或由颅内大血管 70%至 99%狭窄引起的卒中。双臂强化药物治疗均为阿司匹林 325 mg/天,氯吡格雷 75 mg/天,共 90 天,主要强化危险因素管理,目标收缩压<140mmHg(糖尿病患者<130mmHg)和低密度脂蛋白胆固醇<70mg/dL,并进行生活方式改变。根据 log-rank 检验,以 0.05 的α值、80%的效能、调整 2%的失访率和 5%的从药物治疗组到支架置入组的交叉率,为检测主要终点发生率降低 35%,每组需要 382 例患者。
入组于 2008 年 11 月开始,截至 2011 年 3 月 31 日,共入组 451 例患者。
这是第一项比较颅内动脉狭窄患者血管成形术和支架置入与药物治疗的随机卒中预防试验,该研究设计纳入了多种危险因素的强化管理和生活方式改变方案。希望试验结果能为这种高危疾病提供更有效的治疗方法。