Mehta Shyle H, White Timothy G, Shah Kevin A, Lynch Daniel G, Werner Cassidy D, Teron Ina, Link Thomas, Patsalides Athos, Woo Henry H
Department of Neurosurgery, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Manhasset, NY, USA.
Interv Neuroradiol. 2024 Jan 17:15910199231226285. doi: 10.1177/15910199231226285.
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.
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.
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.
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.
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。
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。
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。
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。