Zidan Mousa, Voss Yves Leonard, Wolf Marcel, Keil Fee, Brockmann Carolin, Gronemann Christian, Lehnen Nils Christian, Paech Daniel, Nordmeyer Hannes, Dorn Franziska
Department of Neuroradiology, Bonn University Hospital, Venusberg-Campus1, Gebäude 81, 53127, Bonn, Germany.
Radprax MVZ Nordrhein GmbH, Department of Interventional Neuroradiology, St. Lukas-Klinik, Solingen, Germany.
Clin Neuroradiol. 2025 Mar;35(1):77-85. doi: 10.1007/s00062-024-01455-7. Epub 2024 Sep 3.
Dual-layer stents have fallen into disrepute after several studies reported high rates of in-stent occlusions in acute stroke treatments. The CGuard stent is a new-generation hybrid dual-layer stent that has been designed to provide less thrombogenicity and to prevent peri- and postinterventional emboli. The aim of the study is to evaluate the safety and efficacy of the CGuard stent for the acute treatment of occlusion or high-grade stenosis of the extracranial internal carotid artery (ICA) in patients with acute ischemic stroke (AIS) with and without concomitant intracranial large vessel occlusion (LVO).
All patients who underwent emergent carotid artery stenting (CAS) with the CGuard stent were identified and analyzed from the stroke registries from four tertiary German stroke centers. Clinical, procedural, and imaging data were evaluated. Stent patency within 72 h, intracranial hemorrhage, and modified Rankin score (mRS) at discharge were the safety and efficacy end points.
Overall, ninety-six patients were included (mean age 70.2 ± 11.8, 66 males (68.8%), median NIHSS score at admission 11 (7-17), IV lysis: n = 44 (45.8%)). Stent placement was successful in all patients. Eighty-three (86.4%) patients had tandem occlusions. In-stent occlusion occurred in 5 patients (5.2%) and 3 patients developed early in-stent stenosis (3.1%). Median mRS at discharge was 2 (1-4).
In this multicenter study, the use of the dual-layer CGuard stent for emergent CAS, particularly in tandem occlusions, was safe and resulted in low rates of in-stent occlusions.
在多项研究报告急性卒中治疗中支架内闭塞率较高后,双层支架已声名狼藉。CGuard支架是新一代混合双层支架,其设计目的是降低血栓形成倾向,并预防介入期间及介入后的栓子。本研究旨在评估CGuard支架用于急性缺血性卒中(AIS)伴或不伴颅内大血管闭塞(LVO)患者的颅外颈内动脉(ICA)闭塞或高度狭窄急性治疗的安全性和有效性。
从德国四个三级卒中中心的卒中登记处识别并分析所有接受CGuard支架紧急颈动脉支架置入术(CAS)的患者。评估临床、手术和影像数据。72小时内的支架通畅情况、颅内出血以及出院时的改良Rankin量表评分(mRS)为安全性和有效性终点。
总共纳入96例患者(平均年龄70.2±11.8岁,男性66例(68.8%),入院时NIHSS评分中位数为11(7-17),静脉溶栓:n = 44例(45.8%))。所有患者支架置入均成功。83例(86.4%)患者存在串联闭塞。5例患者(5.2%)发生支架内闭塞,3例患者出现早期支架内狭窄(3.1%)。出院时mRS中位数为2(1-4)。
在这项多中心研究中,双层CGuard支架用于紧急CAS,尤其是在串联闭塞中,是安全的,且支架内闭塞率较低。