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首页> 外文期刊>Interventional neuroradiology: journal of peritherapeutic neuroradiology, surgical procedures and related neurosciences >Initial experience and one-year follow-up with Neuroform Atlas Stent System for the treatment of brain aneurysms
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Initial experience and one-year follow-up with Neuroform Atlas Stent System for the treatment of brain aneurysms

机译:初步经验和一年后随访,治疗脑动脉瘤的治疗

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Introduction The Neuroform Atlas Stent System is a recently introduced modification of the original Neuroform Stent System consisting of a hybrid design with open and closed cells. Initial experience, technical considerations and treatment outcomes including 1-year follow-up using the Atlas stent in combination with coil embolization are reported. Material and methods Thirty patients with 30 unruptured aneurysms were treated with stent reconstruction. Immediate, 4-month and 12-month post-treatment angiography and clinical assessment were performed. Discussion In 29 cases, the stents were delivered and positioned without difficulty in deployment. Technical complications occurred in one patient related to advancement of the stent during delivery. One procedure-related clinical complication occurred with no permanent neurological deficit. On immediate post-treatment angiography, 29 of 30 aneurysms showed Raymond Class I or Class II occlusion. At 1-year follow-up, all 30 patients were clinically stable and 18 of 30 aneurysms showed Raymond Class I complete occlusion. Retreatment was performed in two patients with residual aneurysm. Conclusions The Atlas stent is technically safe and simple to implant and has a low thrombogenic potential. We experienced fewer problems associated with deployment and implantation, thromboembolic complications and hemorrhagic events compared with other types of stents, including braided stents. However, because of its low thrombogenic potential, partially occluded aneurysms or those with aneurysm remnants do not progress to complete occlusion.
机译:简介神经塑造ATLAS支架系统最近引入了由具有开放和闭孔的混合设计组成的原始神经塑造支架系统的修改。报告了初步经验,技术考虑因素和治疗结果,包括使用与线圈栓塞结合使用的Atlas支架的1年随访。材料和方法有30例患有30例未破碎的动脉瘤的患者,用支架重建治疗。立即,4个月和12个月的治疗后治疗后血管造影和临床评估。在29例中讨论,支架被交付并定位,毫无困难地部署。一名患者发生技术并发症与在交付期间支架的进步相关。一种与程序相关的临床并发症,没有永久性神经缺陷。在立即治疗后血管造影,30个动脉瘤中的29例显示Raymond类I或II类闭塞。在1年的随访中,所有30名患者临床稳定,30名动脉瘤显示雷蒙德类我完成闭塞。在两名残留动脉瘤患者中进行了再生。结论Atlas支架在技术上是安全和植入的简单,具有低血栓形成潜力。与其他类型的支架相比,我们经历了与部署和植入,血栓栓塞并发症和出血事件相关的较少问题,包括编织支架。然而,由于其低血栓形成潜力,部分闭塞的动脉瘤或有动脉瘤残留的动脉瘤不会进展以完全闭塞。

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