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首页> 外文期刊>The Lancet >Terutroban versus aspirin in patients with cerebral ischaemic events (PERFORM): a randomised, double-blind, parallel-group trial.
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Terutroban versus aspirin in patients with cerebral ischaemic events (PERFORM): a randomised, double-blind, parallel-group trial.

机译:Teruroban对脑缺血事件(表演)的患者对阿司匹林(表演):随机,双盲,并联群试验。

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BACKGROUND: Patients with ischaemic stroke or transient ischaemic attack (TIA) are at high risk of recurrent stroke or other cardiovascular events. We compared the selective thromboxane-prostaglandin receptor antagonist terutroban with aspirin in the prevention of cerebral and cardiovascular ischaemic events in patients with a recent non-cardioembolic cerebral ischaemic event. METHODS: This randomised, double-blind, parallel-group trial was undertaken in 802 centres in 46 countries. Patients who had an ischaemic stroke in the previous 3 months or a TIA in the previous 8 days were randomly allocated with a central interactive response system to 30 mg per day terutroban or 100 mg per day aspirin. Patients and investigators were masked to treatment allocation. The primary efficacy endpoint was a composite of fatal or non-fatal ischaemic stroke, fatal or non-fatal myocardial infarction, or other vascular death (excluding haemorrhagic death). We planned a sequential statistical analysis of non-inferiority (margin 1.05) followed by analysis of superiority. Analysis was by intention to treat. The study was stopped prematurely for futility on the basis of the recommendation of the Data Monitoring Committee. This study is registered, number ISRCTN66157730. FINDINGS: 9562 patients were assigned to terutroban (9556 analysed) and 9558 to aspirin (9544 analysed); mean follow-up was 28.3 months (SD 7.7). The primary endpoint occurred in 1091 (11%) patients receiving terutroban and 1062 (11%) receiving aspirin (hazard ratio [HR] 1.02, 95% CI 0.94-1.12). There was no evidence of a difference between terutroban and aspirin for the secondary or tertiary endpoints. We recorded some increase in minor bleedings with terutroban compared with aspirin (1147 [12%] vs 1045 [11%]; HR 1.11, 95% CI 1.02-1.21), but no significant differences in other safety endpoints. INTERPRETATION: The trial did not meet the predefined criteria for non-inferiority, but showed similar rates of the primary endpoint with terutroban and aspirin, without safety advantages for terutroban. In a worldwide perspective, aspirin remains the gold standard antiplatelet drug for secondary stroke prevention in view of its efficacy, tolerance, and cost. FUNDING: Servier, France.
机译:背景:患有缺血性卒中或短暂性缺血性发作(TIA)的患者处于经常性中风或其他心血管事件的高风险。我们将选择性血栓素 - 前列腺素受体拮抗剂TeruroBan与阿司匹林进行比较,以预防最近的非心脏病脑缺血事件患者的脑和心血管缺血事件。方法:在46个国家的802个中心进行了随机,双盲,并联赛试验。在前3个月或前8天内进行缺血性脑卒中的患者随机分配给中央互动响应系统,每天30毫克为每天30毫克,每天100毫克阿司匹林。患者和调查人员被掩盖到治疗分配。初级疗效终点是致命或非致命缺血性卒中,致命或非致命心肌梗死或其他血管死亡(不包括出血死亡)的复合物。我们计划了对非劣势(边缘1.05)的连续统计分析,然后分析优越性。分析是意图治疗。这项研究在基于数据监测委员会的建议的基础上过早停止。本研究已注册,数字ISRCTN66157730。结果:9562名患者被分配给Teruroban(9556分析)和9558至阿司匹林(9544分析);平均随访时间为28.3个月(SD 7.7)。初级终点发生在1091(11%)患者接受酸甲磺酸的患者和1062(11%)接受阿司匹林(危害比[HR] 1.02,95%CI 0.94-1.12)。没有证据表明叔特罗巴和阿司匹林对次级或三级终点之间的差异。与阿司匹林相比,我们记录了与Terutroban的轻微出血的一定程度的增加(1147 [12%] [11%]; HR 1.11,95%CI 1.02-1.21),但其他安全终点没有显着差异。解释:试验不符合预定义的非劣种标准,但显示出与Terutroban和阿司匹林的主要终点的速率,而无需褐特罗巴班的安全优势。在全球范围内,阿司匹林仍然是鉴于其疗效,耐受性和成本的次级中风预防金标准抗血小板药物。资金:法国服务者。

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