Evaluation of using a double helical, closed-cell stent-retriever (Skyflow) for thrombectomy procedures in acute arterial occlusion: A preclinical study and a clinical trial

Huan Liu , Yanyan He , Tengfei Zhou , Liangfu Zhu , Yao Zhao , Yonghong Ding , Yingkun He , Tianxiao Li
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Abstract

Background and purpose

Stent retriever thrombectomy is the standard therapeutic approach for ischemic stroke with acute large-vessel occlusion. This study evaluated the safety and efficacy of a new thrombectomy device (Skyflow) in the treatment of acute ischemic stroke.

Methods

After an arterial occlusion model was established, stent-retriever thrombectomy was performed. Digital subtraction angiography (DSA) and autopsy were carried out immediately after thrombectomy in six animals in the acute experimental group. Simulated stent-retriever thrombectomy was performed for three animals in the subacute experimental group, and follow-up angiography and vascular pathological examination were assessed 90 days after the operation. In the clinical trial, 192 patients with intracranial anterior circulation large vessel occlusion, within 8 ​h of symptom onset, were included to undergo thrombectomy with either Skyflow or Solitaire FR stent retriever. Efficacy and safety endpoints were recorded (including successful reperfusion, favorable clinical outcomes, time from puncture to reperfusion, instrument operation success rates and National Institutes of Health Stroke Scale (NIHSS) scores at 7 days for efficacy endpoints, and symptomatic intracranial hemorrhage (sICH), subarachnoid hemorrhage (SAH) and all-cause mortality rates for safety endpoints).

Results

All blood vessels achieved successful recanalization in the animal models. In the clinical trial, successful recanalization was attained in 88.4% of patients of the Skyflow group, which was comparable to that of the Solitaire FR group (82.5%) in the full analysis set of the clinical trial. There were no severe complications on DSA, an animal autopsy, or vessel pathological examination in animal experiments. Additionally, no statistically significant difference was observed between the Skyflow and Solitaire FR groups in the clinical trial regarding the safety endpoints.

Conclusion

This study showed that the new Skyflow stent retriever is safe and effective for the treatment of acute large vessel occlusion, as demonstrated in our animal study and human trial.

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评价在急性动脉闭塞中使用双螺旋闭细胞支架(Skyflow)取栓:临床前研究和临床试验
背景与目的支架取栓是缺血性脑卒中合并急性大血管闭塞的标准治疗方法。本研究评估了一种新型取栓装置(Skyflow)治疗急性缺血性脑卒中的安全性和有效性。方法建立动脉闭塞模型后,行支架取栓术。急性实验组6只动物取栓后立即行数字减影血管造影(DSA)及尸检。亚急性实验组3只动物模拟支架取栓,术后90 d随访血管造影及血管病理检查。在临床试验中,192例颅内前循环大血管闭塞患者,在症状出现8小时内,使用Skyflow或Solitaire FR支架取栓器进行血栓切除术。记录疗效和安全性终点(疗效终点包括再灌注成功、良好的临床结果、穿刺至再灌注时间、器械操作成功率和美国国立卫生研究院卒中量表(NIHSS) 7天评分,安全性终点包括症状性颅内出血(sICH)、蛛网膜下腔出血(SAH)和全因死亡率)。结果动物模型血管再通均成功。在临床试验中,Skyflow组88.4%的患者成功再通,与Solitaire FR组(82.5%)在临床试验的完整分析集中相当。动物实验DSA、动物解剖、血管病理检查均无严重并发症。此外,在临床试验中,Skyflow和Solitaire FR组在安全性终点方面没有统计学上的显著差异。结论我们的动物实验和人体试验表明,新型Skyflow支架回收器治疗急性大血管闭塞是安全有效的。
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来源期刊
Journal of Interventional Medicine
Journal of Interventional Medicine Medicine-General Medicine
CiteScore
1.30
自引率
0.00%
发文量
32
审稿时长
68 days
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