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急性缺血性卒中治疗中MERCI装置失败患者的其他血管内技术的价值:MERCI失败时该怎么办?

Value of Other Endovascular Techniques Among Patients with MERCI Device Failure during the Treatment of Acute Ischemic Stroke: What to do when MERCI fails?

作者信息

Hassan Ameer E, Aman Mansoor M, Chauhdry Saqib A, Grigoryan Mikayel, Tekle Wondwossen G, Rodriguez Gutavo J, Qureshi Adnan I

机构信息

Zeenat Qureshi Stroke Research Center, University of Minnesota, Minneapolis, Minnesota.

出版信息

J Vasc Interv Neurol. 2013 Feb;5(2):9-13.

Abstract

BACKGROUND

The MERCI Retrieval system (Concentric Medical, Mountain View, CA) was the first FDA -approved device for mechanical thrombectomy in patients with acute ischemic stroke. It remains one of the most commonly used devices today despite its failure to restore blood flow in approximately 50% of the occlusions after technically successful deployment and retrieval. It remains unclear whether additional endovascular techniques or continued use of MERCI device can achieve recanalization post- MERCI failure.

OBJECTIVE

To analyze the outcome of continued MERCI retriever use compared to other endovascular techniques after initial failure.

METHODS

Failure of MERCI retriever was defined by successful deployment and retrieval of MERCI across target occlusion without recanalization in a single pass.. Pre- and post- treatment cerebral angiogram was classified using the Qureshi Grading Scale (QGS). Recanalization was defined by a reduction in ≥ 1 grade between pre- and post- treatment cerebral angiogram in the Qureshi Grading Scale (QGS). We ascertained and compared the angiographic and clinical results with continued use of MERCI retriever and other endovascular techniques in patients with MERCI failure.

RESULTS

A total of 40 patients (53% men) had MERCI retrieval in this cohort with a mean age (±standard deviation) of 66.8 years ± 16 years and a mean admission NIHSS score of 16.8 ± 6.7. Of the 40 patients treated with MERCI retrieval, there were 26 patients with MERCI failure. In group 1, there were 11 patients who underwent continued MERCI use and group 2 consisted of 15 patients who had an alternate endovascular technique. There was no significant difference in age, risk factors, or outcomes between the groups. The rate of recanalization (82% versus 80%, p=1.0), asymptomatic intra cerebral hemorrhage (18% versus 13%, p =0.77) and favorable outcome at discharge (27% versus 20%, p =0.66) were similar amongst the two groups.

CONCLUSIONS

Continued attempts using the MERCI device did not result in higher recanalization rates when compared to alternate endovascular treatment modalities following initial MERCI failure. Both techniques produced comparable rates of recanalization and favorable outcome.

摘要

背景

MERCI 取栓系统(同心医疗公司,加利福尼亚州山景城)是首个获得美国食品药品监督管理局(FDA)批准用于急性缺血性中风患者机械取栓的设备。尽管在技术上成功置入和取出该设备后,约 50%的闭塞血管未能恢复血流,但它仍是当今最常用的设备之一。目前尚不清楚额外的血管内技术或继续使用 MERCI 设备能否在 MERCI 取栓失败后实现血管再通。

目的

分析在初次失败后继续使用 MERCI 取栓器与其他血管内技术相比的结果。

方法

MERCI 取栓器失败定义为成功将 MERCI 穿过目标闭塞部位并取出,但单次操作未实现血管再通。治疗前后的脑血管造影使用 Qureshi 分级量表(QGS)进行分类。血管再通定义为 Qureshi 分级量表(QGS)中治疗前后脑血管造影等级降低≥1 级。我们确定并比较了 MERCI 取栓失败患者继续使用 MERCI 取栓器和其他血管内技术的血管造影和临床结果。

结果

该队列中共有 40 例患者(53%为男性)接受了 MERCI 取栓治疗,平均年龄(±标准差)为 66.8 岁±16 岁,入院时美国国立卫生研究院卒中量表(NIHSS)平均评分为 16.8±6.7。在接受 MERCI 取栓治疗的 40 例患者中,有 26 例 MERCI 取栓失败。在第 1 组中,有 11 例患者继续使用 MERCI 取栓器,第 2 组由 15 例采用其他血管内技术的患者组成。两组在年龄、危险因素或结果方面无显著差异。两组的血管再通率(82%对 80%,p = 1.0)、无症状颅内出血发生率(18%对 13%,p = 0.77)和出院时良好预后率(27%对 20%,p = 0.66)相似。

结论

与初次 MERCI 取栓失败后采用其他血管内治疗方式相比,继续尝试使用 MERCI 设备并未带来更高的血管再通率。两种技术的血管再通率和良好预后率相当。

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