Hassan Ameer E, Mohammaden Mahmoud H, Rabah Rani Ramsey, Tekle Wondwossen G
Clinical Research Department, Valley Baptist Medical Center - Harlingen, Harlingen, TX, United States.
Department of Neurology, School of Medicine, University of Texas Rio Grande Valley, Edinburg, TX, United States.
Front Neurol. 2020 Sep 30;11:570100. doi: 10.3389/fneur.2020.570100. eCollection 2020.
Intracranial atherosclerotic disease (ICAD) is a common cause of stroke worldwide. Although there are different endovascular options for the treatment of symptomatic ICAD (sICAD), it is still controversial. Herein, we aim to study the safety and efficacy of a new generation of drug-eluting balloon-mounted stent (DES); Resolute (R) onyx DES in the treatment of sICAD. A prospectively maintained neuroendovascular procedures database in a high-volume comprehensive stroke center was reviewed from October 2019 through January 2020. Patients were included if they had sICAD (≥70% stenosis), failed medical management, and underwent intracranial stenting with R-onyx DES. Technical success was defined as the ability to deploy the device at the desired location and achievement of <30% residual stenosis. The primary outcome was the occurrence of complications within 72 h of the procedure (strokes, ischemic or hemorrhagic; and mortality). Secondary outcomes included rates of symptomatic and angiographic recurrence within 6 months of the procedure. A total of 18 consecutive patients (mean age, 66.6 years; 44.4% were females and 94.4% were Hispanic) were eligible for the analysis. Indication for treatment was recurrent strokes in 13 and recurrent transient ischemic attack (TIA) in 5. A total of 22 symptomatic lesions with a mean baseline stenosis percent (84.9 ± 9.6) were treated using 23 R-onyx DES in 19 procedures. All procedures were done under general anesthesia with 100% technical success, and no reported periprocedural strokes or death. Among 13 patients who had clinical follow-up, 1 (7.7%) patient had TIA. There were no reported ischemic or hemorrhagic strokes. Angiographic follow-up for 9 (50%) patients showed no in-stent restenosis. The use of R-onyx DES in the treatment of sICAD is safe with high technical success rates. Large prospective multicenter trials with long-term follow-up are warranted.
颅内动脉粥样硬化性疾病(ICAD)是全球范围内中风的常见病因。尽管对于有症状的ICAD(sICAD)的治疗存在不同的血管内治疗选择,但仍存在争议。在此,我们旨在研究新一代药物洗脱球囊支架(DES);Resolute(R)玛瑙DES治疗sICAD的安全性和有效性。回顾了2019年10月至2020年1月在一个大容量综合卒中中心前瞻性维护的神经血管介入手术数据库。如果患者患有sICAD(狭窄≥70%)、药物治疗失败且接受了R-玛瑙DES颅内支架置入术,则纳入研究。技术成功定义为能够将装置部署到期望位置且残余狭窄<30%。主要结局是术后72小时内并发症的发生(中风,缺血性或出血性;以及死亡率)。次要结局包括术后6个月内症状性复发和血管造影复发率。共有18例连续患者(平均年龄66.6岁;44.4%为女性,94.4%为西班牙裔)符合分析条件。治疗指征为13例复发性中风和5例复发性短暂性脑缺血发作(TIA)。在19例手术中使用23个R-玛瑙DES治疗了22个有症状病变,平均基线狭窄百分比为(84.9±9.6)。所有手术均在全身麻醉下进行,技术成功率为100%,且未报告围手术期中风或死亡。在13例进行临床随访的患者中,1例(7.7%)患者发生TIA。未报告缺血性或出血性中风。9例(50%)患者的血管造影随访显示无支架内再狭窄。使用R-玛瑙DES治疗sICAD是安全的,技术成功率高。有必要进行大型前瞻性多中心长期随访试验。