Department of Medicine, Brain Research Center, Division of Neurology, University of British Columbia, Vancouver, BC, Canada.
Int J Stroke. 2011 Apr;6(2):164-75. doi: 10.1111/j.1747-4949.2010.00573.x. Epub 2011 Jan 26.
Small subcortical strokes, also known as lacunar strokes, comprise more than 25% of brain infarcts, and the underlying vasculopathy is the most common cause of vascular cognitive impairment. How to optimally prevent stroke recurrence and cognitive decline in S3 patients is unclear. The aim of the Secondary Prevention of Small Subcortical Strokes study (Trial registration: NCT00059306) is to define strategies for reducing stroke recurrence, cognitive decline, and major vascular events.
Secondary Prevention of Small Subcortical Strokes is a randomised, multicentre clinical trial (n = 3000) being conducted in seven countries, and sponsored by the US NINDS/NIH. Patients with symptomatic small subcortical strokes in the six-months before and an eligible lesion on magnetic resonance imaging are simultaneously randomised, in a 2 × 2 factorial design, to antiplatelet therapy--325 mg aspirin daily plus 75 mg clopidogrel daily, vs. 325 mg aspirin daily plus placebo, double-blind--and to one of two levels of systolic blood pressure targets--'intensive' (<130 mmHg) vs. 'usual' (130-149 mmHg). Participants are followed for an average of four-years. Time to recurrent stroke (ischaemic or haemorrhagic) is the primary outcome and will be analysed separately for each intervention. The secondary outcomes are the rate of cognitive decline and major vascular events. The primary and most secondary outcomes are adjudicated centrally by those unaware of treatment assignment.
Secondary Prevention of Small Subcortical Strokes will address several important clinical and scientific questions by testing two interventions in patients with recent magnetic resonance imaging-defined lacunar infarcts, which are likely due to small vessel disease. The results will inform the management of millions of patients with this common vascular disorder.
小的皮质下卒中,也称为腔隙性卒中,占脑梗死的 25%以上,其潜在的血管病变是血管性认知障碍的最常见原因。如何在 S3 患者中最佳地预防中风复发和认知能力下降尚不清楚。次级预防小皮质下卒中研究(试验注册:NCT00059306)的目的是定义减少中风复发、认知能力下降和主要血管事件的策略。
次级预防小皮质下卒中是一项在七个国家进行的随机、多中心临床试验(n = 3000),由美国国立神经病学、语言障碍和中风研究所(NINDS)/美国国立卫生研究院(NIH)赞助。在六个月前有症状性小皮质下卒中和磁共振成像上有一个合格病变的患者,同时以 2×2 析因设计,随机分配到抗血小板治疗-每日 325 毫克阿司匹林加每日 75 毫克氯吡格雷,与每日 325 毫克阿司匹林加安慰剂,双盲-和两个收缩压目标水平之一-“强化”(<130 mmHg)与“常规”(130-149 mmHg)。参与者平均随访四年。复发性中风(缺血性或出血性)的时间是主要结局,将分别针对每种干预进行分析。次要结局是认知能力下降和主要血管事件的发生率。主要和大多数次要结局由那些不了解治疗分配的中心进行裁决。
次级预防小皮质下卒中将通过测试两种干预措施来解决几个重要的临床和科学问题,这些干预措施适用于磁共振成像定义的近期腔隙性梗死患者,这些患者可能是由于小血管疾病引起的。研究结果将为管理这种常见血管疾病的数百万患者提供信息。