首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Comparative analysis of CGUARD embolic prevention stent with Casper-RX and Wallstent for the treatment of carotid artery stenosis
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Comparative analysis of CGUARD embolic prevention stent with Casper-RX and Wallstent for the treatment of carotid artery stenosis

机译:Casper-Rx和Wallstent治疗颈动脉狭窄的Cguard栓塞预防支架的比较分析

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摘要

Stent protected Angioplasty of extracranial carotid artery stenosis using the dual-layered CGUARD stent is a novel treatment option. In this study we evaluate the feasibility and the safety of the CGUARD in symptomatic and asymptomatic patients in comparison to Casper-RX and Wallstent. This is a multi-center study of consecutive patients treated with the CGUARD, Casper-RX and Wallstent at two German high volume neurovascular centers between April 2017 and May 2018. Patient characteristics, neuroimaging data and angiographic outcome were retrospectively analyzed. The primary end points of the study were acute occlusion of the carotid stent and symptomatic intracerebral hemorrhage (sICH). Carotid artery stenting was performed in 76 patients; of those 26 (34%) were treated with the CGUARD, 25 (33%) with Casper-RX, and 25 (33%) with Wallstent. In 58/76 (76%) cases carotid artery stenosis was symptomatic with a median baseline National Institutes of Health Stroke Scale of 4. Angioplasty and stenting as part of a mechanical thrombectomy for acute ischemic stroke was performed in 25/76 (33%) patients. Baseline patient characteristics were similar between the treatment groups, except for a higher portion of scheduled cases in the Casper-RX group. There were no significant differences in the rate of acute in stent occlusions (CGUARD, 2/26 (8%); Casper-RX, 1/25(4%), Wallstent, 1/25 (4%)) and postinterventional sICH (1/26 (4%), 0/25(0%), 0/25 (0%)). Clinical outcome at discharge did not differ between groups. Treatment of carotid artery stenosis using CGUARD is feasible with a good safety profile comparable to that of Casper-RX and Wallstent. (C) 2020 Elsevier Ltd. All rights reserved.
机译:使用双层Cguard支架的颅外颈动脉狭窄的支架受保护的血管成形术是一种新型治疗选择。在这项研究中,我们与Casper-Rx和Wallstent相比,评估了患有症状和无症状患者的可行性和安全性。这是在2017年4月和2018年4月至2018年5月间在德国大批量神经血管中心治疗的连续患者的多中心研究。回顾性分析患者特征,神经影像数据和血管造影结果。研究的主要终点是颈动脉支架和症状脑出血(SICH)的急性闭塞。颈动脉支架在76名患者中进行;将这些26(34%)用Cuard,25(33%)用Casper-Rx处理,25(33%)用壁式处理。在58/76(76%)病例中,颈动脉狭窄是对4.血管成形术和止动术的血管成形术,作为急性缺血性卒中的一部分,在25/76(33%)中进行血管成形术和支架。(33%)耐心。除了Casper-Rx组中的较高部分预定案例之外,基线患者特征在治疗组之间具有相似。支架闭塞的急性速度没有显着差异(Cguard,2/26(8%); Casper-Rx,1/25(4%),壁垒,1/25(4%))和初期性Sich( 1/26(4%),0/25(0%),0/25(0%))。排出的临床结果在组之间没有差异。使用Cguard处理颈动脉狭窄是可行的,与Casper-Rx和Wallstent的良好安全性曲线相当。 (c)2020 elestvier有限公司保留所有权利。

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