Next-generation transcarotid artery revascularization: TransCarotid flOw Reversal Cerebral Protection And CGUARD MicroNET-Covered Embolic Prevention Stent System To Reduce Strokes - TOPGUARD Study.

Mariusz Trystula, Isabelle VAN Herzeele, Ralf Kolvenbach, Lukasz Tekieli, Charlotte Fonteyne, Adam Mazurek, Karolina Dzierwa, Jakub Chmiel, Julie Lindsay, Tomasz Kwiatkowski, Adam Hydzik, Maksymilian Oplawski, Krzysztof Bederski, Piotr Musialek
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Abstract

Background: Stent-assisted carotid artery revascularization employing surgical cutdown for transcervical access and dynamic flow reversal (TCAR) is gaining popularity. TCAR, despite maximized intra-procedural cerebral protection, shows a marked excess of 30-day neurologic complications in symptomatic vs. asymptomatic stenoses. The TCAR conventional single-layer stent (free-cell area 5.89mm2) inability to seal embologenic lesions may be particularly relevant after the flow reversal neuroprotection is terminated.

Methods: We evaluated peri-procedural and 30-day major adverse cerebral and cardiac events (MACCE) of TCAR (ENROUTE, SilkRoad Medical) paired with MicroNET-covered neuroprotective stent (CGuard, InspireMD) in consecutive patients at elevated risk of complications with transfemoral/transradial filter-protected stenting (increased lesion-related and/or access-related risk). CGuard (MicroNET free cell area ≈0.02-0.03 mm2) has level-1 evidence for reducing intra- and abolishing post-procedural lesion-related cerebral embolism.

Results: One hundred and six increased-risk patients (age 72 [61-76] years, median [Q1-Q3]; 60.4% symptomatic, 49.1% diabetic, 36.8% women, 61.3% left-sided index lesion) were enrolled in three vascular surgery centers. Angiographic stenosis severity was 81 (75-91)%, lesion length 21 (15-26)mm, increased-risk lesional characteristics 87.7%. Study stent use was 100% (no other stent types). 74.5% lesions were predilated; post-dilatation rate was 90.6%. Flow reversal duration was 8 (5-11)min. One stroke (0.9%) occurred in an asymptomatic patient prior to establishing neuroprotection (index lesion disruption with the sheath insertion wire); there were no other peri-procedural MACCE. No further adverse events occurred by 30-days. 30-day stent patency was 100% with normal velocities and absence of any in-stent material by Duplex Doppler.

Conclusions: Despite a high proportion of increased-risk lesions and clinically symptomatic patients in this study, TCAR employing the MicroNET-covered anti-embolic stent showed 30-day MACCE rate <1%. This suggests a clinical role for combining maximized intra-procedural prevention of cerebral embolism by dynamic flow reversal with anti-embolic stent prevention of peri- and post-procedural cerebral embolism (TOPGUARD NCT04547387).

新一代经颈动脉血管重建术:减少脑卒中的经颈动脉血流逆转脑保护和 CGUARD 微网覆盖栓塞预防支架系统 - TOPGUARD 研究。
背景:支架辅助颈动脉血运重建术采用经颈椎入路手术切口和动态血流逆转(TCAR)的方法越来越受欢迎。尽管 TCAR 最大限度地保护了术中大脑,但在有症状与无症状狭窄的情况下,30 天神经系统并发症的发生率明显偏高。TCAR 传统的单层支架(自由细胞面积为 5.89 平方毫米)无法封闭栓塞病变,这一点在血流逆转神经保护终止后可能尤为重要:我们评估了TCAR(ENROUTE,SilkRoad Medical公司)与MicroNET覆盖神经保护支架(CGuard,InspireMD公司)在经股动脉/经桡动脉过滤器保护支架术并发症风险较高(病变相关风险和/或通路相关风险增加)的连续患者中的围手术期和30天主要脑和心脏不良事件(MACCE)。CGuard(MicroNET游离细胞面积≈0.02-0.03 mm2)在减少术中和消除术后病变相关脑栓塞方面具有一级证据:三家血管外科中心共招募了16名高风险患者(年龄72 [61-76]岁,中位数[Q1-Q3];60.4%无症状,49.1%糖尿病,36.8%女性,61.3%左侧指数病变)。血管造影狭窄严重程度为 81(75-91)%,病变长度为 21(15-26)毫米,高危病变特征为 87.7%。研究支架使用率为 100%(无其他支架类型)。74.5%的病变进行了扩张前处理;扩张后处理率为90.6%。血流逆转持续时间为 8 (5-11) 分钟。一名无症状患者在建立神经保护前发生了一次中风(0.9%)(用鞘插入线破坏了指数病变);没有发生其他围手术期澳门巴黎人娱乐官网。30 天内未再发生其他不良事件。30天的支架通畅率为100%,速度正常,双相多普勒显示支架内无任何物质:尽管本研究中高风险病变和有临床症状的患者比例较高,但采用 MicroNET 包覆抗栓塞支架的 TCAR 30 天 MACCE 率为 100%。
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