Sorensen P S, Pedersen H, Marquardsen J, Petersson H, Heltberg A, Simonsen N, Munck O, Andersen L A
Stroke. 1983 Jan-Feb;14(1):15-22.
Two hundred and three patients, 148 males and 55 females, who during the last month before admission had experienced at least one reversible cerebral ischemic attack of less than 72 hours duration, were randomly assigned to treatment with either acetylsalicylic acid (ASA) 1000 mg daily (101 patients) or placebo (102 patients). The average follow-up period was 25 months. The two treatment groups were comparable with respect to age, sex, associated diseases, risk factors, number and duration of cerebral ischemic attacks. No statistically significant differences were found between the treatment groups as to the primary end point: stroke or death (ASA group 20.8%, placebo group 16.7%). Occurrence of transient ischemic attacks during the treatment period was not reduced by ASA treatment, whereas there was a trend suggesting fewer myocardial infarctions in the ASA group (5.9%) than in the placebo group (13.7%). The difference, however, was not statistically significant (p = 0.10). We were thus unable to demonstrate any favorable influence of ASA 1000 mg daily in patients with reversible ischemic attacks. This study does not, of course, prove that ASA treatment is ineffective in stroke prevention.
203例患者,其中男性148例,女性55例,在入院前的最后一个月内经历过至少一次持续时间少于72小时的可逆性脑缺血发作,被随机分配接受每日1000毫克阿司匹林(ASA)治疗(101例患者)或安慰剂治疗(102例患者)。平均随访期为25个月。两个治疗组在年龄、性别、相关疾病、危险因素、脑缺血发作的次数和持续时间方面具有可比性。在主要终点方面,即中风或死亡,治疗组之间未发现统计学上的显著差异(ASA组为20.8%,安慰剂组为16.7%)。ASA治疗并未减少治疗期间短暂性脑缺血发作的发生,然而,有一个趋势表明ASA组(5.9%)的心肌梗死发生率低于安慰剂组(13.7%)。不过,这种差异在统计学上并不显著(p = 0.10)。因此,我们无法证明每日1000毫克ASA对可逆性缺血发作患者有任何有益影响。当然,这项研究并不能证明ASA治疗在预防中风方面无效。