Effect of IV Thrombolysis With Alteplase in Patients With Vessel Occlusion in the WAKE-UP Trial.

IF 8.5 1区 医学 Q1 CLINICAL NEUROLOGY Neurology Pub Date : 2025-01-28 Epub Date: 2024-12-20 DOI:10.1212/WNL.0000000000209871
Ivana Galinovic, Jochen B Fiebach, Florent Boutitie, Bastian Cheng, Tae-Hee Cho, Martin Ebinger, Matthias Endres, Christian Enzinger, Jens Fiehler, Ian Ford, Johannes Gregori, Matthias Günther, Robin Lemmens, Keith W Muir, N Nighoghossian, Pascal Roy, Claus Z Simonsen, Vincent N Thijs, Anke Wouters, Christian Gerloff, Götz Thomalla, Salvador Pedraza
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Abstract

Background and objectives: Data from randomized trials on the treatment effect of pure thrombolysis in patients with vessel occlusion are lacking. We examined data from a corresponding subsample of patients from the multicenter, randomized, placebo-controlled WAKE-UP trial to determine whether MRI-guided IV thrombolysis with alteplase in unknown-onset ischemic stroke benefits patients presenting with vessel occlusion.

Methods: Patients with an acute ischemic lesion visible on MRI diffusion-weighted imaging but no marked parenchymal hyperintensity on fluid-attenuated inversion recovery images were randomized to treatment with IV alteplase or placebo. The primary end point was a favorable outcome defined by a modified Rankin Scale score of 0-1 at 90 days after stroke. We investigated the interaction between vessel status and treatment effect using an unconditional logistic regression model. Treatment effects (adjusted odds ratio [aOR]) and their 95% CI were compared in patients with and without any vessel occlusion (AVO) and large vessel occlusion (LVO).

Results: 185 patients (mean age 64.5 years, 46% female, median NIH Stroke Scale score 9, median time between last seen well and MRI 10.26 hours) received treatment and presented with an occlusion. 98 (20%) had LVO (defined as occlusion of the internal carotid artery, middle cerebral artery trunk, or combination). A favorable outcome was observed in 30 of 94 patients with AVO (31.9%) in the alteplase group and in 18 of 91 (19.8%) in the placebo group (aOR 2.04, 95% CI 1.00-4.18). In the subgroup of patients with LVO, a favorable outcome was observed in 16 of 53 (30.2%) in the alteplase group and in 7 of 44 (15.9%) in the placebo group (aOR 2.08, 95% CI 0.71-6.10). Treatment with alteplase was associated with higher odds of favorable outcomes with no heterogeneity of treatment effect between patients with AVO and patent vessel (p = 0.56), or between patients with and without LVO (p = 0.69).

Discussion: Although the WAKE-UP study was not powered to demonstrate treatment efficacy in patient subpopulations, this subgroup analysis points to a benefit of MRI-guided thrombolysis in patients with unknown-onset ischemic stroke, independent of vessel occlusion.

Clinical trial registration: Registered at ClinicalTrials.gov with unique identifier NCT01525290 (clinicaltrials.gov/study/NCT01525290). The study was first posted on February 2, 2012; the first patient was enrolled on September 24, 2012.

Classification of evidence: This study provides Class II evidence that for patients with unknown-onset ischemic stroke with AVO, MRI-guided treatment with IV tissue plasminogen activator improves outcomes.

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阿替普酶静脉溶栓对 WAKE-UP 试验中血管闭塞患者的影响
背景和目的:缺乏纯溶栓治疗血管闭塞患者疗效的随机试验数据。我们检查了来自多中心、随机、安慰剂对照的wake试验患者相应亚样本的数据,以确定mri引导下阿替普酶静脉溶栓治疗不明原因缺血性卒中是否有利于血管闭塞患者。方法:在MRI弥散加权成像上可见急性缺血性病变,但在液体衰减反转恢复图像上没有明显的实质高信号的患者随机分为静脉注射阿替普酶或安慰剂两组。主要终点是卒中后90天的有利结果,由改进的Rankin量表评分0-1定义。我们使用无条件逻辑回归模型研究了血管状态和治疗效果之间的相互作用。比较有无血管闭塞(AVO)和大血管闭塞(LVO)患者的治疗效果(调整优势比[aOR])及其95% CI。结果:185例患者(平均年龄64.5岁,46%为女性,NIH卒中量表中位评分为9分,最后一次看清楚和MRI之间的中位时间为10.26小时)接受治疗并出现闭塞。98例(20%)有LVO(定义为颈内动脉、大脑中动脉干或两者闭塞)。阿替普酶组94例AVO患者中有30例(31.9%)和安慰剂组91例患者中有18例(19.8%)的预后良好(aOR 2.04, 95% CI 1.00-4.18)。在LVO患者亚组中,阿替普酶组53名患者中有16名(30.2%)获得了良好的预后,安慰剂组44名患者中有7名(15.9%)获得了良好的预后(aOR 2.08, 95% CI 0.71-6.10)。阿替普酶治疗与良好结局的几率较高相关,在有AVO和血管通畅的患者之间(p = 0.56),或有和没有LVO的患者之间(p = 0.69),治疗效果没有异质性。讨论:尽管wake -起床研究没有证明治疗在患者亚群中的疗效,但该亚组分析指出,mri引导下的溶栓治疗对未知发病的缺血性卒中患者有益处,独立于血管闭塞。临床试验注册:在ClinicalTrials.gov注册,唯一标识符NCT01525290 (clinicaltrials.gov/study/NCT01525290)。这项研究于2012年2月2日首次发布;首例患者于2012年9月24日入组。证据分类:本研究提供了II类证据,表明对于不明原因的缺血性卒中AVO患者,mri引导下静脉组织纤溶酶原激活剂治疗可改善预后。
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来源期刊
Neurology
Neurology 医学-临床神经学
CiteScore
12.20
自引率
4.00%
发文量
1973
审稿时长
2-3 weeks
期刊介绍: Neurology, the official journal of the American Academy of Neurology, aspires to be the premier peer-reviewed journal for clinical neurology research. Its mission is to publish exceptional peer-reviewed original research articles, editorials, and reviews to improve patient care, education, clinical research, and professionalism in neurology. As the leading clinical neurology journal worldwide, Neurology targets physicians specializing in nervous system diseases and conditions. It aims to advance the field by presenting new basic and clinical research that influences neurological practice. The journal is a leading source of cutting-edge, peer-reviewed information for the neurology community worldwide. Editorial content includes Research, Clinical/Scientific Notes, Views, Historical Neurology, NeuroImages, Humanities, Letters, and position papers from the American Academy of Neurology. The online version is considered the definitive version, encompassing all available content. Neurology is indexed in prestigious databases such as MEDLINE/PubMed, Embase, Scopus, Biological Abstracts®, PsycINFO®, Current Contents®, Web of Science®, CrossRef, and Google Scholar.
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