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在普拉格雷单药治疗下使用表面改性血流导向装置治疗的未破裂颅内远端动脉瘤的两年随访结果。

Two year follow-up of distal unruptured intracranial aneurysms treated with a surface modified flow diverter under prasugrel monotherapy.

机构信息

Interventional Neuroradiology, Universidade de São Paulo Faculdade de Medicina de Ribeirão Preto, Ribeirao Preto, Brazil.

Interventional Neuroradiology, Hospital Israelita Albert Einstein, Sao Paulo, Brazil.

出版信息

J Neurointerv Surg. 2024 Oct 14;16(11):1163-1166. doi: 10.1136/jnis-2023-020397.

Abstract

BACKGROUND

A new generation of modified surface flow diverters (FDs) and monotherapy using new antiplatelets may reduce both ischemic and hemorrhagic complications during the treatment of intracranial aneurysms. Previous preliminary safety analysis of distal unruptured intracranial aneurysms treated with the FD p48 MW HPC (phenox-Wallaby, Bochum, Germany) under antiplatelet monotherapy with prasugrel showed promising results. However, the long term outcomes of distal intracranial aneurysms treated with FDs under antiplatelet monotherapy are not known.

METHODS

This was a single center, prospective, pivotal, open single arm study. The primary (safety) endpoint was absence of any new neurological deficits after treatment until the 24 month follow-up. The primary (efficacy) endpoint was the incidence of complete aneurysm occlusion 24 months after treatment. The secondary (efficacy) endpoints were any incidence of aneurysm dome reduction 24 months after treatment.

RESULTS

21 patients harboring 27 distal aneurysms of the anterior circulation were included. No patient had neurologic deficits in the time from treatment to the 24 month follow-up. Complete aneurysm occlusion occurred in 20 (74%) of 27 aneurysms at the 24 month follow-up. Four aneurysms (14.8%) had dome reduction, and three aneurysms (11.1%) remained unchanged.

CONCLUSIONS

In this pilot trial, treatment of distal unruptured intracranial aneurysms with an FD under monotherapy with prasugrel, followed by monotherapy with aspirin, appeared to be safe and effective. Randomized studies with long term follow-up are needed to confirm these results.

摘要

背景

新一代改良表面血流导向装置(FD)和新型抗血小板药物单药治疗可能会降低颅内动脉瘤治疗过程中的缺血性和出血性并发症。先前使用普拉格雷进行抗血小板单药治疗的 p48MW HPC(phenox-Wallaby,德国波鸿)FD 治疗未破裂颅内远端动脉瘤的初步安全性分析显示出良好的结果。然而,使用抗血小板单药治疗 FD 治疗的颅内远端动脉瘤的长期结果尚不清楚。

方法

这是一项单中心、前瞻性、关键、开放的单臂研究。主要(安全性)终点是治疗后至 24 个月随访期间无任何新的神经功能缺损。主要(疗效)终点是治疗后 24 个月完全闭塞动脉瘤的发生率。次要(疗效)终点是治疗后 24 个月任何动脉瘤瘤顶缩小的发生率。

结果

共纳入 21 例患者的 27 个前循环远端动脉瘤。从治疗到 24 个月随访期间,没有患者出现神经功能缺损。27 个动脉瘤中,有 20 个(74%)在 24 个月随访时完全闭塞。4 个动脉瘤(14.8%)瘤顶缩小,3 个动脉瘤(11.1%)保持不变。

结论

在这项初步试验中,使用 FD 进行抗血小板单药治疗(随后进行单药阿司匹林治疗)治疗未破裂颅内远端动脉瘤似乎是安全有效的。需要进行长期随访的随机研究来证实这些结果。

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