Effect of Intravenous Tirofiban Versus Placebo on First-Pass Successful Reperfusion in Endovascular Stroke Thrombectomy: Insights From the RESCUE BT Randomized Clinical Trial.

IF 5 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Journal of the American Heart Association Pub Date : 2024-11-05 Epub Date: 2024-11-04 DOI:10.1161/JAHA.124.036350
Junjie Yuan, Hanming Ge, Zhaojun Tao, Huijie An, Qin Han, Jeffrey L Saver, Thanh N Nguyen, Simin Zhou, An Mao, Yuelu Wu, Raul Gomes Nogueira, Yaxuan Sun, Shunfu Jiang, Liping Wei, Xinmin Fu, Yongjie Bai, Shunyu Yang, Wei Hu, Guling Zhang, Chengde Pan, Shuai Zhang, Lin Qiao, Qiong Chen, Hongfei Sang, Zhongming Qiu, Fengfu Wu, Mingze Chang, Zhongfan Ruan
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引用次数: 0

Abstract

Background: First-pass successful reperfusion (FPSR), defined as a successful/complete reperfusion achieved after a single thrombectomy pass, is predictive of favorable outcome in patients with acute ischemic stroke with large-vessel occlusion. It is unknown whether intravenous tirofiban is effective in increasing the rate of FPSR in acute anterior large-vessel occlusion stroke.

Methods and results: Patients who had acute large-vessel occlusion stroke presenting within 24 hours and underwent endovascular thrombectomy were analyzed from the RESCUE BT (Intravenous Tirofiban for Patients With Large Vessel Occlusion Stroke) clinical trial, of which the main analysis was neutral. The RESCUE BT trial randomized patients to receive either intravenous tirofiban or placebo before endovascular thrombectomy. The primary end point was FPSR, defined as successful reperfusion (extended thrombolysis in cerebral infarction scale 2b50, 2c, or 3) at first thrombectomy attempt. A modified Poisson regression analysis assessed the association between intravenous tirofiban treatment and FPSR. Of 948 enrolled patients, 463 patients were randomized to the tirofiban group and 485 to the placebo group. The mean age was 67 years, and 41.0% of the patients were women. FPSR was achieved more often in the tirofiban group (30.5% versus 23.5%; adjusted risk ratio, 1.24 [95% CI, 1.01-1.51]; P=0.04). FPSR was associated with a favorable shift to lower modified Rankin Scale disability levels at 90 days (common odds ratio, 1.42 [95% CI, 1.08-1.86]; P=0.01).

Conclusions: In this post hoc analysis of the RESCUE BT trial, treatment with intravenous tirofiban before endovascular thrombectomy was associated with increased FPSR in patients with acute ischemic stroke due to large-vessel occlusion in the anterior circulation. FPSR was associated with reduced 90-day levels of disability.

Registration: URL: http://chictr.org; Unique Identifier: ChiCTR-INR-17014167.

静脉注射替罗非班与安慰剂对血管内卒中血栓切除术首次成功再灌注的影响:RESCUE BT 随机临床试验的启示。
背景:首次成功再灌注(FPSR)是指单次血栓切除术后成功/完全再灌注,可预测大血管闭塞性急性缺血性卒中患者的良好预后。目前尚不清楚静脉注射替罗非班是否能有效提高急性前大静脉闭塞性卒中的 FPSR 率:对在 24 小时内发病并接受血管内血栓切除术的急性大血管闭塞性卒中患者进行了分析,这些患者来自 RESCUE BT(大血管闭塞性卒中患者静脉注射替罗非班)临床试验,主要分析结果为中性。RESCUE BT试验随机分配患者在血管内血栓切除术前接受静脉注射替罗非班或安慰剂。主要终点是FPSR,定义为首次血栓切除尝试时再灌注成功(脑梗塞扩展溶栓量表2b50、2c或3)。改良泊松回归分析评估了静脉注射替罗非班治疗与 FPSR 之间的关系。在948名入选患者中,463名患者被随机分配到替罗非班组,485名患者被随机分配到安慰剂组。平均年龄为 67 岁,41.0% 的患者为女性。替罗非班组实现 FPSR 的比例更高(30.5% 对 23.5%;调整风险比为 1.24 [95% CI, 1.01-1.51];P=0.04)。在90天时,FPSR与改良Rankin量表残疾程度向较低水平的有利转变相关(普通风险比为1.42 [95% CI, 1.08-1.86];P=0.01):在这项RESCUE BT试验的事后分析中,在血管内血栓切除术前静脉注射替罗非班与前循环大血管闭塞导致的急性缺血性卒中患者的FPSR增加有关。FPSR与90天残疾程度的降低有关:URL: http://chictr.org; Unique Identifier:ChiCTR-INR-17014167。
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
Journal of the American Heart Association
Journal of the American Heart Association CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
9.40
自引率
1.90%
发文量
1749
审稿时长
12 weeks
期刊介绍: As an Open Access journal, JAHA - Journal of the American Heart Association is rapidly and freely available, accelerating the translation of strong science into effective practice. JAHA is an authoritative, peer-reviewed Open Access journal focusing on cardiovascular and cerebrovascular disease. JAHA provides a global forum for basic and clinical research and timely reviews on cardiovascular disease and stroke. As an Open Access journal, its content is free on publication to read, download, and share, accelerating the translation of strong science into effective practice.
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