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首页> 外文期刊>The Lancet >Early administration of aspirin in patients treated with alteplase for acute ischaemic stroke: A randomised controlled trial
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Early administration of aspirin in patients treated with alteplase for acute ischaemic stroke: A randomised controlled trial

机译:阿替普酶治疗急性缺血性卒中患者的早期服用阿司匹林:一项随机对照试验

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Background Thrombolysis with intravenous alteplase is the only approved treatment for acute ischaemic stroke. After alteplase-induced recanalisation, reocclusion occurs in 14-34% of patients, probably because of platelet activation. Early administration of antiplatelet therapy after alteplase could reduce the risk of reocclusion and improve outcome. We compared the effects of early addition of intravenous aspirin to alteplase with standard alteplase without aspirin. Methods In this multicentre, randomised, open-label trial with blind-endpoint assessment, patients with acute ischaemic stroke treated with alteplase were randomly assigned to 300 mg intravenous aspirin within 90 min after start of alteplase treatment or to no additional treatment. In both groups, oral antiplatelet therapy was started 24 h after alteplase treatment. The primary endpoint was favourable outcome, defined as a score of 0-2 on the modified Rankin scale at 3 months. This trial is registered with the Netherlands Trial Register (NTR822). Findings Between July 29, 2008, and April 20, 2011, 642 patients (322 patients aspirin, 320 patients standard treatment) of the targeted 800 patients were enrolled. At that time, the trial was terminated prematurely because of an excess of symptomatic intracranial haemorrhage (SICH) and no evidence of benefit in the aspirin group. At 3 months, 174 (54.0%) patients in the aspirin group versus 183 (57.2%) patients in the standard treatment group had a favourable outcome (absolute difference -3.2%, 95% CI -10.8 to 4.2; crude relative risk 0.94, 0.82 to 1.09, p=0.42). Adjusted odds ratio was 0.91 (95% CI 0.66-1.26, p=0.58). SICH occurred more often in the aspirin group (14 [4.3%] patients) than in the standard treatment group (five [1.6%]; absolute difference 2.8%, 95% CI 0.2-5.4; p=0.04). SICH was more often the cause of poor outcome in the aspirin group compared with the standard treatment group (11 vs 1, p=0.006). Interpretation Early administration of intravenous aspirin in patients with acute ischaemic stroke treated with alteplase does not improve outcome at 3 months and increases the risk of SICH. The results of this trial do not support a change of the current guidelines, which advise to start antiplatelet therapy 24 h after alteplase. Funding The Dutch Heart Foundation.
机译:背景技术静脉使用阿替普酶溶栓术是唯一批准的急性缺血性卒中治疗方法。阿替普酶诱导的小管再通后,14-34%的患者会发生再闭塞,这可能是由于血小板活化所致。阿替普酶治疗后及早给予抗血小板治疗可降低再次闭塞的风险并改善预后。我们比较了将早期阿司匹林静脉注射阿司匹林与标准阿替普酶不含阿司匹林的效果。方法在这项多中心,开放标签,盲点评估的随机试验中,使用阿替普酶治疗的急性缺血性中风患者在开始接受阿替普酶治疗后的90分钟内被随机分配至300 mg静脉内阿司匹林或不进行其他治疗。两组均在阿替普酶治疗后24小时开始口服抗血小板治疗。主要终点为良好的预后,定义为改良Rankin量表在3个月时的0-2分。该试验已在荷兰审判注册(NTR822)中进行了注册。研究结果在2008年7月29日至2011年4月20日之间,纳入了800例目标患者中的642例患者(322例阿司匹林,320例标准治疗)。当时,由于有症状的颅内出血过多(SICH)且阿司匹林组没有获益的证据,该试验提前终止。在3个月时,阿司匹林组的174(54.0%)例患者与标准治疗组的183(57.2%)例患者有良好的预后(绝对差异-3.2%,95%CI -10.8至4.2;相对危险度0.94, 0.82至1.09,p = 0.42)。调整后的优势比为0.91(95%CI 0.66-1.26,p = 0.58)。与标准治疗组(5 [1.6%];绝对差异2.8%,95%CI 0.2-5.4; p = 0.04)相比,阿司匹林组(14 [4.3%]患者)发生SICH的频率更高。与标准治疗组相比,阿司匹林组中SICH常常是不良预后的原因(11 vs 1,p = 0.006)。解释对于阿替普酶治疗的急性缺血性卒中患者,尽早静脉注射阿司匹林不能改善3个月的预后并增加SICH的风险。该试验的结果不支持当前指南的更改,该指南建议在阿替普酶治疗后24小时开始抗血小板治疗。资助荷兰心脏基金会。

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