Department of Neurology, University Hospital and University of Bern, Bern, Switzerland.
Institute of Diagnostic and Interventional Neuroradiology, University Hospital and University of Bern, Bern, Switzerland.
Int J Stroke. 2022 Jul;17(6):698-705. doi: 10.1177/17474930211048768. Epub 2021 Oct 14.
Whether treatment with intravenous alteplase prior to mechanical thrombectomy (MT) in acute ischemic stroke patients with large vessel occlusion is beneficial remains unclear.
To determine whether patients experiencing acute ischemic stroke due to occlusion of the intracranial internal carotid artery or the M1 segment of the middle cerebral artery who are referred to an endovascular stroke center and who are candidates for intravenous alteplase will have non-inferior functional outcome at 90 days when treated with MT alone (direct MT) with stent retrievers compared to patients treated with combined intravenous thrombolysis (IVT) with alteplase plus MT (IVT + MT) with stent retrievers.
To randomize 404 patients 1:1 to direct MT or combined IVT+MT.
A multicenter, prospective, randomized, open-label, blinded-endpoint (PROBE) trial utilizing an adaptive statistical design.
The primary efficacy endpoint is functional independence (modified Rankin Scale 0-2) at 90 days. Secondary clinical efficacy outcomes include change in National Institutes of Health Stroke Scale score from baseline to day 1 and health-related quality of life at 90 days. Secondary technical efficacy outcomes include successful reperfusion prior to start of MT and time from randomization to successful reperfusion. Safety outcomes include all serious adverse events, symptomatic intracranial hemorrhage, and mortality up to 90 days.
SWIFT DIRECT will inform physicians whether direct MT in acute ischemic stroke patients with large vessel occlusion is equally or more efficacious than combined treatment with intravenous alteplase and MT.
ClinicalTrials.gov Identifier: NCT03192332.
在伴有大血管闭塞的急性缺血性脑卒中患者中,机械取栓(MT)前静脉内使用阿替普酶的治疗是否有益尚不清楚。
确定对于因颅内颈内动脉或大脑中动脉 M1 段闭塞而导致急性缺血性脑卒中并被转送至血管内卒中中心且适合静脉内阿替普酶治疗的患者,与接受联合静脉溶栓(阿替普酶 IVT)加 MT(IVT+MT)联合支架取栓治疗的患者相比,单独接受 MT(直接 MT)治疗的患者在 90 天时是否具有非劣效的功能结局。
将 404 例患者以 1:1 的比例随机分配至直接 MT 或联合 IVT+MT。
一项多中心、前瞻性、随机、开放标签、盲终点(PROBE)试验,采用适应性统计设计。
主要疗效终点为 90 天时的功能独立性(改良 Rankin 量表 0-2 分)。次要临床疗效结局包括从基线到第 1 天的国立卫生研究院卒中量表评分变化和 90 天时的健康相关生活质量。次要技术疗效结局包括 MT 开始前的成功再灌注和随机分组至成功再灌注的时间。安全性结局包括所有严重不良事件、症状性颅内出血和 90 天内的死亡率。
SWIFT DIRECT 将告知医生直接 MT 在伴有大血管闭塞的急性缺血性脑卒中患者中的疗效是否与联合使用阿替普酶和 MT 的治疗相当或更有效。
ClinicalTrials.gov 标识符:NCT03192332。