首页> 外文期刊>The Lancet >Thrombectomy alone versus intravenous alteplase plus thrombectomy in patients with stroke: an open-label blinded-outcome, randomised non-inferiority trial
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Thrombectomy alone versus intravenous alteplase plus thrombectomy in patients with stroke: an open-label blinded-outcome, randomised non-inferiority trial

机译:单纯血栓切除术与静脉注射阿替普酶加血栓切除术治疗脑卒中患者的比较:一项开放标签、盲法结局、随机非劣效性试验

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Background Whether thrombectomy alone is equally as effective as intravenous alteplase plus thrombectomy remains controversial. We aimed to determine whether thrombectomy alone would be non-inferior to intravenous alteplase plus thrombectomy in patients presenting with acute ischaemic stroke. Methods In this multicentre, randomised, open-label, blinded-outcome trial in Europe and Canada, we recruited patients with stroke due to large vessel occlusion confirmed with CT or magnetic resonance angiography admitted to endovascular centres. Patients were randomly assigned (1:1) via a centralised web server using a deterministic minimisation method to receive stent-retriever thrombectomy alone or intravenous alteplase plus stent-retriever thrombectomy. In both groups, thrombectomy was initiated as fast as possible with any commercially available Solitaire stent-retriever revascularisation device (Medtronic, Irvine, CA, USA). In the combined treatment group, intravenous alteplase (0.9 mg/kg bodyweight, maximum dose 90 mg per patient) was administered as early as possible after randomisation for 60 min with 10 of the calculated dose given as an initial bolus. Personnel assessing the primary outcome were masked to group allocation; patients and treating physicians were not. The primary binary outcome was a score of 2 or less on the modified Rankin scale at 90 days. We assessed the non-inferiority of thrombectomy alone versus intravenous alteplase plus thrombectomy in all randomly assigned and consenting patients using the one-sided lower 95 confidence limit of the Mantel-Haenszel risk difference, with a prespecified non-inferiority margin of 12. The main safety endpoint was symptomatic intracranial haemorrhage assessed in all randomly assigned and consenting participants. This trial is registered with ClinicalTrials.gov, NCT03192332, and is closed to new participants. Findings Between Nov 29, 2017, and May 7, 2021, 5215 patients were screened and 423 were randomly assigned, of whom 408 (201 thrombectomy alone, 207 intravenous alteplase plus thrombectomy) were included in the primary efficacy analysis. A modified Rankin scale score of 0-2 at 90 days was reached by 114 (57) of 201 patients assigned to thrombectomy alone and 135 (65) of 207 patients assigned to intravenous alteplase plus thrombectomy (adjusted risk difference -7 .3, 95 CI -16.6 to 2.1, lower limit of one-sided 95 CI -15.1, crossing the non-inferiority margin of - 12). Symptomatic intracranial haemorrhage occurred in five (2) of 201 patients undergoing thrombectomy alone and seven (3) of 202 patients receiving intravenous alteplase plus thrombectomy ( risk difference -1.0, 95 CI -4.8 to 2 .7). Successful reperfusion was less common in patients assigned to thrombectomy alone (182 91 of 201 vs 199 96 of 207, risk difference -5.1, 95 CI -10.2 to 0. 0, p=0.047). Interpretation Thrombectomy alone was not shown to be non-inferior to intravenous alteplase plus thrombectomy and resulted in decreased reperfusion rates. These results do not support omitting intravenous alteplase before thrombectomy in eligible patients. Copyright (C) 2022 Elsevier Ltd. All rights reserved.
机译:背景:单独血栓切除术是否与静脉注射阿替普酶加血栓切除术同样有效仍存在争议。我们旨在确定在急性缺血性卒中患者中,单独血栓切除术是否不劣于静脉注射阿替普酶加血栓切除术。方法 在欧洲和加拿大进行的这项多中心、随机、开放标签、盲法结局试验中,我们招募了经 CT 或磁共振血管造影证实的血管内中心大血管闭塞导致卒中患者。患者通过集中式网络服务器随机分配 (1:1),使用确定性最小化方法接受单独支架取栓器血栓切除术或静脉注射阿替普酶加支架取栓器血栓切除术。在两组中,使用任何市售的单人纸支架取回器血运重建装置(美敦力,尔湾,加利福尼亚州,美国)尽快开始血栓切除术。在联合治疗组中,随机分组后尽早静脉注射阿替普酶(0.9 mg/kg体重,每位患者最大剂量90 mg),持续60分钟,计算剂量的10%作为初始推注给药。评估主要结局的人员被掩盖到分组分配中;患者和主治医生则不然。主要的二元结局是90天时改良Rankin量表的得分为2分或更低。我们使用Mantel-Haenszel风险差的单侧95%置信下限,评估了在所有随机分配和同意的患者中,单独血栓切除术与静脉注射阿替普酶联合血栓切除术的非劣效性,预先设定的非劣效性边际为12%。主要安全终点是在所有随机分配和同意的受试者中评估的症状性颅内出血。该试验已在 ClinicalTrials.gov、NCT03192332注册,不对新参与者开放。结果 2017 年 11 月 29 日至 2021 年 5 月 7 日期间,筛选了 5215 例患者,随机分配了 423 例,其中 408 例(单独取栓术 201 例,静脉注射阿替普酶加血栓切除术 207 例)被纳入主要疗效分析。201 例单独接受血栓切除术的患者中有 114 例 (57%) 和静脉注射阿替普酶加血栓切除术的 207 例患者中有 135 例 (65%) 在 90 天时达到 0-2 的改良 Rankin 量表评分(校正风险差 -7 .3%,95% CI -16.6 至 2.1,单侧 95% CI 下限 -15.1%,越过非劣效性边缘 -12%)。在仅接受血栓切除术的 201 例患者中,有 5 例 (2%) 发生有症状的颅内出血,在接受静脉注射阿替普酶加血栓切除术的 202 例患者中,有 7 例 (3%) 发生症状性颅内出血(风险差异 -1.0%,95% CI -4.8 至 2 .7)。在单独接受血栓切除术的患者中,再灌注成功率较低(201例中有182例[91%]比207例中有199例[96%],风险差-5.1%,95%CI -10.2至0。0,p=0.047)。解释 单纯血栓切除术并不劣于静脉注射阿替普酶加血栓切除术,并导致再灌注率降低。这些结果不支持在符合条件的患者血栓切除术前省略静脉注射阿替普酶。版权所有 (C) 2022 Elsevier Ltd.保留所有权利。

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