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用于急性大血管闭塞抢救性支架置入的Onyx Frontier™和Resolute Onyx™药物洗脱球囊扩张式支架的单中心研究结果

Single-center outcomes of Onyx Frontier™ and Resolute Onyx™ drug-eluting balloon-mounted stents for rescue stenting for acute large vessel occlusion.

作者信息

Mehta Shyle H, White Timothy G, Shah Kevin A, Lynch Daniel G, Werner Cassidy D, Teron Ina, Link Thomas, Patsalides Athos, Woo Henry H

机构信息

Department of Neurosurgery, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Manhasset, NY, USA.

出版信息

Interv Neuroradiol. 2024 Jan 17:15910199231226285. doi: 10.1177/15910199231226285.

Abstract

BACKGROUND

In cases where mechanical thrombectomy (MT) fails, rescue stenting may be necessary to achieve reperfusion; however, the lack of standardized techniques or devices poses a challenge. This series aims to present our early experience with the Onyx Frontier™ and Resolute Onyx™ balloon-mounted drug-eluting stents for rescue stenting.

METHODS

A retrospective chart review was performed of all patients who underwent rescue stenting, in the setting of failed MT, using Onyx Frontier™ or Resolute Onyx™ stents at a single institution. Technical details, procedural complications, and patient outcomes were recorded for each case.

RESULTS

Twenty-two Onyx Frontier™ and Resolute Onyx™ stents were deployed in 18 patients undergoing rescue stenting. Stent locations included the middle cerebral artery (36.4%), internal carotid artery (18.2%), vertebral artery (22.7%), and basilar artery (22.7%). The average National Institutes of Health Stroke Scale score before MT was 13.8 (range 0-31). The median initial modified Rankin Scale (mRS) score was zero, while the median mRS score at follow-up was three. Successful reperfusion, as assessed by TICI scores, was achieved in 43.8% of patients for TICI 3, 43.8% for TICI 2C, and 12.5% for TICI 2B. Post-revascularization, 16.7% of patients experienced hemorrhage, of which one patient (5.6%) had symptomatic hemorrhage.

CONCLUSIONS

Onyx Frontier™ and Resolute Onyx™ stents are well suited for rescue stenting in cases of failed MT. These balloon-mounted drug-eluting stents exhibit excellent navigability, rendering them appropriate for rescue revascularization procedures. Our findings demonstrate that these stents confer a high degree of technical success.

摘要

背景

在机械取栓(MT)失败的情况下,可能需要进行补救性支架置入以实现再灌注;然而,缺乏标准化技术或设备构成了一项挑战。本系列旨在介绍我们使用Onyx Frontier™和Resolute Onyx™球囊载药支架进行补救性支架置入的早期经验。

方法

对在单一机构接受补救性支架置入(在MT失败的情况下)并使用Onyx Frontier™或Resolute Onyx™支架的所有患者进行回顾性病历审查。记录每个病例的技术细节、手术并发症和患者结局。

结果

在18例接受补救性支架置入的患者中部署了22个Onyx Frontier™和Resolute Onyx™支架。支架置入位置包括大脑中动脉(36.4%)、颈内动脉(18.2%)、椎动脉(22.7%)和基底动脉(22.7%)。MT前美国国立卫生研究院卒中量表平均评分为13.8(范围0 - 31)。初始改良Rankin量表(mRS)中位数评分为零,而随访时mRS中位数评分为3。根据脑梗死溶栓(TICI)评分评估,43.8%的患者实现了TICI 3级成功再灌注,43.8%为TICI 2C级,12.5%为TICI 2B级。血管再通后,16.7%的患者发生出血,其中1例患者(5.6%)出现症状性出血。

结论

Onyx Frontier™和Resolute Onyx™支架非常适合MT失败病例的补救性支架置入。这些球囊载药支架具有出色的可操作性,使其适用于补救性血管再通手术。我们的研究结果表明,这些支架具有高度的技术成功率。

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