利用三维锥束CT血管造影评估扩张后在颈动脉微网覆盖支架植入中的作用。

Luca Ginanni Corradini, Luciano Maresca, Pierleone Lucatelli, Simone Balocco, Adolfo D'Onofrio, Matteo Stefanini
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引用次数: 0

摘要

背景:本研究旨在通过锥形束CT扫描评估新型MicroNet覆膜支架在保护性颈动脉支架(PCAS)扩张后的作用和安全性。方法:2020年3月至2022年3月,根据CT血管造影结果,根据以下标准纳入研究:根据NASCET指数,无症状患者颈动脉狭窄70% - 99%,有症状患者颈动脉狭窄50% - 99%。使用FilterWire EZ™(Boston Scientific, Natick, MA, USA)栓塞保护系统(EPS), PCAS由两名具有至少8年血管内介入经验的介入放射科医生执行。每位患者均在支架置入后进行扩张。最后,第三位放射科医生(不参与介入手术)评估锥束CT扫描并计算残余狭窄。在手术后30天内记录主要和次要并发症。结果:共纳入192例患者,其中男性121例,平均年龄73±10岁,均行支架置入术后扩张。所有程序都取得了技术上的成功。本研究中注意到的不良事件仅限于192例患者中有3例(1.6%)发生术中短暂性脑缺血发作,并显示迅速完全恢复。本研究使用的扩张后球囊直径分别为:5.0 mm(30.3%)、5.5 mm(39.3%)和6 mm(30.3%)。由于扩张后,我们发现最终管腔面积显著增加。在所有斑块亚型中均可观察到类似的改善。结论:受保护的CAS扩张后是安全的,无论狭窄斑块如何,其截面积都有显著改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of post-dilatation in carotid MicroNet-covered stent implantation, evaluated using 3D cone-beam CT angiography.

Background: This study aims to assess the role and safety of post-dilatation in protected carotid artery stenting (PCAS) using the new MicroNet-covered 2nd-generation stent assessed by cone beam CT scans.

Methods: From March 2020 to March 2022, patients were enrolled in the study according to CT angiography results based on the following criteria: Evidence of 70% to 99% carotid stenosis in asymptomatic patients and 50% to 99% in symptomatic patients, per the NASCET index. Using a FilterWire EZ™ (Boston Scientific, Natick, MA, USA) embolic protection system (EPS), MicroNet-covered stent PCAS was performed by two interventional radiologists with at least 8 years of experience in endovascular intervention. Each patient underwent post-dilatation following stent placement. Finally, a third radiologist (not participating in the interventional procedures) evaluated the cone beam CT scans and calculated residual stenosis. Major and minor complications were recorded in the 30 days following the procedure.

Results: A total of 192 patients (121 male, mean age 73±10 years) were included in the study, and all patients received post-dilatation following stent implantation. Technical successes were achieved in all procedures. Adverse events noted in this study were limited to periprocedural transient ischemic attacks that occurred in three out of 192 patients (1.6%) and showed a swift complete recovery. The post-dilatation balloon diameters used in the study were: 5.0 mm (30.3%), 5.5 mm (39.3%) and 6 mm (30.3%). Optimized postdilatation resulted in a significant increase in the final luminal area. Similar improvements were observed in all subtypes of plaque.

Conclusions: Post-dilatation in protected CAS is safe and induces a significant improvement in the cross-sectional area regardless of the stenotic plaque.

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