University Institute of Diagnostic and Interventional Neuroradiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
University Institute of Diagnostic and Interventional and Pediatric Radiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Clin Neuroradiol. 2023 Mar;33(1):237-244. doi: 10.1007/s00062-022-01209-3. Epub 2022 Sep 7.
Double-layer stents show promising results in preventing periinterventional and postinterventional embolic events in elective settings of carotid artery stenting (CAS). We report a single-center experience with the CGuard stent in the treatment of acute ischemic stroke (AIS) due to symptomatic internal carotid artery (ICA) stenosis or occlusion with or without intracranial occlusion.
We retrospectively analyzed all patients who received a CGuard stent in the setting of AIS at our institution. Neuroimaging and clinical data were analyzed with the following primary endpoints: technical feasibility, acute and delayed stent occlusion or thrombosis, distal embolism, symptomatic intracranial hemorrhage (sICH) and functional outcome at 3 months.
In 33 patients, stenting with the CGuard was performed. Stent deployment was successful in all patients (28 with tandem occlusions, 5 with isolated ICA occlusion). Transient acute in-stent thrombus formation occurred in three patients (9%) without early stent occlusion. Delayed, asymptomatic stent occlusion was seen in 1 patient (3%) after 49 days. Asymptomatic periinterventional distal emboli occurred in 2 patients (6%), 1 patient experienced a transient ischemic attack 79 days after the procedure and 1 patient (3%) developed sICH. Favorable clinical outcome (mRS 0-2) at 3 months was achieved in 12 patients (36%) and the mortality rate was 24%.
The CGuard use in emergencies was technically feasible, the safety has to be confirmed by further multicentric studies.
双层支架在预防颈动脉支架置入术(CAS)择期治疗中的围手术期和术后栓塞事件方面显示出良好的效果。我们报告了在有或无颅内闭塞的症状性颈内动脉(ICA)狭窄或闭塞的急性缺血性脑卒中(AIS)患者中使用 CGuard 支架的单中心经验。
我们回顾性分析了在我院接受 CGuard 支架治疗 AIS 的所有患者。使用以下主要终点分析神经影像学和临床数据:技术可行性、急性和迟发性支架闭塞或血栓形成、远端栓塞、症状性颅内出血(sICH)和 3 个月时的功能结局。
33 例患者接受了 CGuard 支架置入术。所有患者(28 例为串联闭塞,5 例为单纯 ICA 闭塞)均成功置入支架。3 名患者(9%)出现短暂的急性支架内血栓形成,但无早期支架闭塞。1 名患者(3%)在 49 天后出现无症状的迟发性支架闭塞。2 名患者(6%)出现无症状的围手术期远端栓塞,1 名患者在术后 79 天发生短暂性脑缺血发作,1 名患者(3%)发生 sICH。3 个月时,12 名患者(36%)获得了良好的临床结局(mRS 0-2),死亡率为 24%。
CGuard 在紧急情况下使用技术上是可行的,其安全性需要进一步的多中心研究来证实。