Departments of Medicine and Therapeutics, Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.
Lancet Neurol. 2010 May;9(5):489-97. doi: 10.1016/S1474-4422(10)70060-0. Epub 2010 Mar 22.
Few randomised clinical trials have investigated the use of antithrombotic drugs for early secondary prevention of stroke or transient ischaemic attack in patients with intracranial atherosclerotic stenosis. Microembolic signals, detected by transcranial doppler, are a surrogate marker of future stroke risk and have been used to show treatment efficacy in patients with extracranial carotid stenosis. We aimed to investigate whether treatment with clopidogrel plus aspirin reduced the number of microembolic signals detected with transcranial doppler ultrasound compared with aspirin alone in patients with recent stroke.
The clopidogrel plus aspirin for infarction reduction in acute stroke or transient ischaemic attack patients with large artery stenosis and microembolic signals (CLAIR) trial was a randomised, open-label, blinded-endpoint trial. Between Oct 28, 2003, and Nov 19, 2008, patients with acute ischaemic stroke or transient ischaemic attack who had symptomatic large artery stenosis in the cerebral or carotid arteries and in whom microembolic signals were present on transcranial doppler were randomly assigned within 7 days of symptom onset to receive clopidogrel (300 mg for the first day, then 75 mg daily) plus aspirin (75-160 mg daily) or aspirin alone (75-160 mg daily) for 7 days. Patients were randomly assigned in blocks of four or six by use of a randomisation website. Monitoring of microembolic signals on transcranial doppler was done on days 2 and 7. The primary endpoint was the proportion of patients who had microembolic signals on day 2. Analysis was by modified intention to treat. All analyses were done by an investigator masked to both patient identity and the day the recording was taken. This trial is registered with the Centre for Clinical Trials, Chinese University of Hong Kong, number CUHK_CCT00164.
100 patients were randomly assigned to clopidogrel plus aspirin (n=47) or aspirin monotherapy (n=53). 93 of 100 patients had symptomatic intracranial stenosis in either the intracranial internal carotid artery or the middle cerebral artery: 45 of 46 in the dual therapy group and 48 of 52 in the monotherapy group. At day 2, 14 of 45 patients in the dual therapy group and 27 of 50 patients in the monotherapy group for whom data were available had at least one microembolic signal on transcranial doppler (relative risk reduction 42.4%, 95% CI 4.6-65.2; p=0.025). Adverse events were similar in the two groups. No patients had intracranial or severe systemic haemorrhage, but two patients in the dual therapy group had minor haemorrhages.
Combination therapy with clopidogrel and aspirin is more effective than aspirin alone in reducing microembolic signals in patients with predominantly intracranial symptomatic stenosis. Clinical trials are now warranted to investigate whether this combination treatment also results in a reduction in stroke incidence.
很少有随机临床试验研究过抗血栓药物在颅内动脉粥样硬化狭窄患者中的早期二级预防卒中或短暂性脑缺血发作的作用。经颅多普勒检测到的微栓子信号是未来卒中风险的替代标志物,并已用于显示颅外颈动脉狭窄患者的治疗效果。我们旨在研究氯吡格雷联合阿司匹林治疗是否比单独使用阿司匹林减少了近期卒中患者经颅多普勒超声检测到的微栓子信号数量。
氯吡格雷联合阿司匹林减少急性卒中和短暂性脑缺血发作患者大动脉狭窄和微栓子信号的试验(CLAIR)是一项随机、开放标签、盲终点试验。在 2003 年 10 月 28 日至 2008 年 11 月 19 日期间,患有大脑或颈动脉症状性大动脉狭窄且经颅多普勒检测到微栓子信号的急性缺血性卒中和短暂性脑缺血发作患者在症状出现后 7 天内随机分配接受氯吡格雷(第 1 天 300mg,然后每天 75mg)加阿司匹林(每天 75-160mg)或单独使用阿司匹林(每天 75-160mg)治疗 7 天。患者按使用随机网站的四或六块分组随机分配。在第 2 和第 7 天进行经颅多普勒微栓子信号监测。主要终点是第 2 天有微栓子信号的患者比例。分析采用改良意向治疗。所有分析均由一名对患者身份和记录日期均不知情的研究者进行。这项试验在中国香港中文大学临床试验中心注册,编号为 CUHK_CCT00164。
100 名患者被随机分配接受氯吡格雷联合阿司匹林(n=47)或阿司匹林单药治疗(n=53)。100 名患者中有 93 名患有颅内或大脑中动脉症状性颅内动脉狭窄:联合治疗组 46 名中的 45 名和单药治疗组 52 名中的 48 名。在第 2 天,联合治疗组的 45 名患者中有 14 名和单药治疗组的 50 名患者中有 27 名患者经颅多普勒检测到至少有一个微栓子信号(相对风险降低 42.4%,95%CI 4.6-65.2;p=0.025)。两组的不良事件相似。没有患者发生颅内或严重系统性出血,但联合治疗组有两名患者发生轻微出血。
氯吡格雷联合阿司匹林治疗比单独使用阿司匹林更能有效减少主要为颅内症状性狭窄患者的微栓子信号。现在需要进行临床试验来研究这种联合治疗是否也能降低卒中发生率。