Suppr超能文献

机械取栓术后辅助动脉内注射替奈普酶的安全性:ALLY 试验性研究

Safety of Adjunctive Intraarterial Tenecteplase Following Mechanical Thrombectomy: The ALLY Pilot Trial.

作者信息

Zaidi Syed F, Castonguay Alicia C, Zaidat Osama O, Jadhav Ashutosh P, Sheth Sunil A, Haussen Diogo C, Nguyen Thanh N, Burgess Richard E, Alhajala Hisham S, Gharaibeh Khaled, Salahuddin Hisham, Rao Rahul, Oliver Marion J, Jumaa Mouhammad A

机构信息

Department of Neurology, University of Toledo, OH (S.F.Z., A.C.C., R.E.B., H.S.A., K.G., R.R., M.A.J.).

Department of Neurology, ProMedica Toledo Hospital, OH (S.F.Z., R.R., M.A.J.).

出版信息

Stroke. 2025 Feb;56(2):355-361. doi: 10.1161/STROKEAHA.124.048846. Epub 2025 Jan 8.

Abstract

BACKGROUND

Recent studies suggest that the use of adjunctive intraarterial alteplase after mechanical thrombectomy (MT) may improve outcomes; however, there are limited data on the use of intraarterial tenecteplase, a newer-generation lytic, in this acute ischemic stroke patient population. Here, we evaluate the use of intraarterial tenecteplase in the ALLY pilot study (Adjunctive Intraarterial Tenecteplase Following Mechanical Thrombectomy).

METHODS

ALLY was a prospective, single-center, nonrandomized pilot study assessing the feasibility and safety of intraarterial tenecteplase up to 4.5 mg in acute ischemic stroke-large vessel occlusion MT patients with incomplete recanalization. The primary safety end point was any intracranial hemorrhage and neurological worsening by ≥4 points on the National Institutes of Health Stroke Scale within 24 hours of treatment with intraarterial tenecteplase. A post hoc analysis was performed with a control cohort of MT patients (ALLY MT) not receiving intraarterial tenecteplase.

RESULTS

From April 2022 to July 2023, 218 MTs were performed at ProMedica Hospital (Toledo, OH), of which 20 patients were enrolled in ALLY. The mean age was 66.1±13.8 years, with 35% women. Median baseline National Institutes of Health Stroke Scale scores and Alberta Stroke Program Early CT Scores were 13 (interquartile range, 9-18.8) and 10 (interquartile range, 9-10), respectively. IV thrombolysis was administered in 55%. Most patients presented with middle cerebral artery occlusion (90%). Post-MT modified Treatment in Cerebral Ischemia grade was 2b and 2c in 11 and 9 patients, respectively. Final modified Treatment in Cerebral Ischemia 2b, 2c, and 3 was achieved in 55% (11/20), 35% (7/20), and 10% (2/20), respectively. Any intracranial hemorrhage was observed in 11 patients; however, only 1 patient had symptomatic intracranial hemorrhage. A favorable functional outcome (modified Rankin Scale score, 0-2) at 90 days was achieved in 50%. No difference in intracranial hemorrhage rates was observed between the ALLY and ALLY MT cohorts.

CONCLUSIONS

The use of adjunctive intraarterial tenecteplase up to 4.5 mg in patients with acute ischemic stroke with incomplete reperfusion post-MT is feasible and was not associated with increased rates of hemorrhage. Larger, randomized studies are needed to assess the safety and efficacy of intraarterial tenecteplase in this population.

REGISTRATION

URL: https://www.clinicaltrials.gov; Unique identifier: NCT05172934.

摘要

背景

近期研究表明,机械取栓(MT)后使用辅助动脉内阿替普酶可能改善预后;然而,关于新一代溶栓药物动脉内替奈普酶在急性缺血性脑卒中患者群体中的应用数据有限。在此,我们在ALL Y试点研究(机械取栓后辅助动脉内替奈普酶)中评估动脉内替奈普酶的应用。

方法

ALL Y是一项前瞻性、单中心、非随机试点研究,评估在急性缺血性脑卒中 - 大血管闭塞且再通不完全的MT患者中使用高达4.5mg动脉内替奈普酶的可行性和安全性。主要安全终点是在动脉内替奈普酶治疗后24小时内发生任何颅内出血以及美国国立卫生研究院卒中量表评分神经功能恶化≥4分。对未接受动脉内替奈普酶的MT患者对照组(ALL Y MT)进行事后分析。

结果

2022年4月至2023年7月,在普罗梅迪卡医院(俄亥俄州托莱多)进行了218例MT,其中20例患者纳入ALL Y研究。平均年龄为66.1±13.8岁,女性占35%。基线美国国立卫生研究院卒中量表评分中位数和阿尔伯塔卒中项目早期CT评分分别为13(四分位间距,9 - 18.8)和10(四分位间距,9 - 10)。55%的患者接受了静脉溶栓治疗。大多数患者表现为大脑中动脉闭塞(90%)。MT后改良脑缺血治疗分级为2b级和2c级的患者分别有11例和9例。最终改良脑缺血治疗分级达到2b级、2c级和3级的患者分别占55%(11/20)、35%(7/20)和10%(2/20)。11例患者观察到任何颅内出血;然而,只有1例患者有症状性颅内出血。90天时50%的患者获得了良好的功能预后(改良Rankin量表评分,0 - 2)。ALL Y组和ALL Y MT组之间未观察到颅内出血率的差异。

结论

在MT后再灌注不完全的急性缺血性脑卒中患者中使用高达4.5mg的辅助动脉内替奈普酶是可行的,且与出血率增加无关。需要更大规模的随机研究来评估动脉内替奈普酶在该人群中的安全性和有效性。

注册信息

网址:https://www.clinicaltrials.gov;唯一标识符:NCT05172934。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验