Alteplase for Posterior Circulation Ischemic Stroke at 4.5 to 24 Hours.

IF 78.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL New England Journal of Medicine Pub Date : 2025-04-03 DOI:10.1056/NEJMoa2413344
Shenqiang Yan, Ying Zhou, Maarten G Lansberg, David S Liebeskind, Changzheng Yuan, Han Yu, Fujian Chen, Hongfang Chen, Bing Zhang, Lingqun Mao, Xiaoling Zhang, Xiaona Wang, Xuting Zhang, Yi Chen, Huan Zhou, Wansi Zhong, Yaode He, Kun Chen, Jianbing Wang, Hui Chen, Yuhui Huang, Bruce C V Campbell, Min Lou
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Abstract

Background: The effects and risks of the use of intravenous thrombolysis between 4.5 and 24 hours after the onset of a posterior circulation ischemic stroke are not well studied.

Methods: In a trial conducted in China, we randomly assigned patients with posterior circulation stroke, without extensive early hypodensity on computed tomography and with no planned thrombectomy, to receive alteplase (0.9 mg per kilogram of body weight; maximum dose, 90 mg) or standard medical treatment 4.5 to 24 hours after the onset of symptoms. The primary outcome was functional independence (defined as a score of 0 to 2 on the modified Rankin scale; scores range from 0 to 6, with higher scores indicating greater disability) at 90 days. The key safety outcomes were symptomatic intracranial hemorrhage and death.

Results: A total of 234 patients were enrolled; 117 were assigned to the alteplase group and 117 to the standard-treatment group. The median score on the National Institutes of Health Stroke Scale was 3 (interquartile range, 2 to 6) (scores range from 0 to 42, with higher scores indicating greater neurologic deficit). A higher percentage of patients in the alteplase group than in the standard-treatment group had functional independence at 90 days (89.6% vs. 72.6%; adjusted risk ratio, 1.16; 95% confidence interval [CI], 1.03 to 1.30; P = 0.01). The incidence of symptomatic intracranial hemorrhage within 36 hours was 1.7% in the alteplase group and 0.9% in the standard-treatment group. At 90 days, 5.2% of the patients in the alteplase group and 8.5% of those in the standard-treatment group had died.

Conclusions: Among Chinese patients with mainly mild posterior circulation stroke who did not receive thrombectomy, alteplase administered 4.5 to 24 hours after stroke onset resulted in a higher frequency of functional independence at 90 days than standard medical care. (Funded by the National Natural Science Foundation of China; EXPECTS ClinicalTrials.gov number, NCT05429476.).

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阿替普酶治疗4.5 ~ 24小时后循环缺血性卒中。
背景:后循环缺血性卒中发病后4.5 - 24小时内静脉溶栓的效果和风险尚未得到很好的研究。方法:在中国进行的一项试验中,我们随机分配后循环卒中患者,这些患者在计算机断层扫描上没有广泛的早期低密度,也没有计划取栓,接受阿替普酶治疗(每公斤体重0.9 mg;最大剂量为90毫克)或在症状出现后4.5至24小时进行标准药物治疗。主要结局是功能独立性(定义为在修改的Rankin量表上得分0到2分;评分范围从0到6,分数越高表明残疾程度越严重)。主要的安全结局是症状性颅内出血和死亡。结果:共纳入234例患者;117例被分配到阿替普酶组,117例被分配到标准治疗组。美国国立卫生研究院卒中量表的中位数得分为3分(四分位数范围为2到6分)(得分范围为0到42分,得分越高表明神经功能缺陷越严重)。阿替普酶组患者在90天功能独立的比例高于标准治疗组(89.6% vs. 72.6%;调整后风险比为1.16;95%置信区间[CI], 1.03 ~ 1.30;p = 0.01)。36小时内症状性颅内出血发生率阿替普酶组为1.7%,标准治疗组为0.9%。90天时,阿替普酶组和标准治疗组分别有5.2%和8.5%的患者死亡。结论:在未接受血栓切除术的中国轻度后循环卒中患者中,在卒中发作后4.5至24小时给予阿替普酶治疗的患者在90天内功能独立的频率高于标准医疗护理。(国家自然科学基金资助;expectclinicaltrials .gov号码:NCT05429476)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
New England Journal of Medicine
New England Journal of Medicine 医学-医学:内科
CiteScore
145.40
自引率
0.60%
发文量
1839
审稿时长
1 months
期刊介绍: The New England Journal of Medicine (NEJM) stands as the foremost medical journal and website worldwide. With an impressive history spanning over two centuries, NEJM boasts a consistent publication of superb, peer-reviewed research and engaging clinical content. Our primary objective revolves around delivering high-caliber information and findings at the juncture of biomedical science and clinical practice. We strive to present this knowledge in formats that are not only comprehensible but also hold practical value, effectively influencing healthcare practices and ultimately enhancing patient outcomes.
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