Departments of 1 Radiology.
Neurology, and.
J Neurosurg. 2017 Jul;127(1):81-88. doi: 10.3171/2015.6.JNS15311. Epub 2016 Oct 14.
OBJECTIVE The long-term effectiveness of endovascular treatment of large and giant wide-neck aneurysms using traditional endovascular techniques has been disappointing, with high recanalization and re-treatment rates. Flow diversion with the Pipeline Embolization Device (PED) has been recently used as a stand-alone therapy for complex aneurysms, showing significant improvement in effectiveness while demonstrating a similar safety profile to stent-supported coil treatment. However, relatively little is known about its long-term safety and effectiveness. Here the authors report on the 3-year safety and effectiveness of flow diversion with the PED in a prospective cohort of patients with large and giant internal carotid artery aneurysms enrolled in the Pipeline for Uncoilable or Failed Aneurysms (PUFS) trial. METHODS The PUFS trial is a prospective study of 107 patients with 109 aneurysms treated with the PED. Primary effectiveness and safety end points were demonstrated based on independently monitored 180-day clinical and angiographic data. Patients were enrolled in a long-term follow-up protocol including 1-, 3-, and 5-year clinical and imaging follow-up. In this paper, the authors report the midstudy (3-year) effectiveness and safety data. RESULTS At 3 years posttreatment, 74 subjects with 76 aneurysms underwent catheter angiography as required per protocol. Overall, complete angiographic aneurysm occlusion was observed in 71 of these 76 aneurysms (93.4% cure rate). Five aneurysms were re-treated, using either coils or additional PEDs, for failure to occlude, and 3 of these 5 were cured by the 3-year follow-up. Angiographic cure with one or two treatments of Pipeline embolization alone was therefore achieved in 92.1%. No recanalization of a previously completely occluded aneurysm was noted on the 3-year angiograms. There were 3 (2.6%) delayed device- or aneurysm-related serious adverse events, none of which led to permanent neurological sequelae. No major or minor late-onset hemorrhagic or ischemic cerebrovascular events or neurological deaths were observed in the 6-month through 3-year posttreatment period. Among 103 surviving patients, 85 underwent functional outcome assessment in which modified Rankin Scale scores of 0-1 were demonstrated in 80 subjects. CONCLUSIONS Pipeline embolization is safe and effective in the treatment of complex large and giant aneurysms of the intracranial internal carotid artery. Unlike more traditional endovascular treatments, flow diversion results in progressive vascular remodeling that leads to complete aneurysm obliteration over longer-term follow-up without delayed aneurysm recanalization and/or growth. Clinical trial registration no.: NCT00777088 (clinicaltrials.gov).
使用传统的血管内技术治疗大、巨型宽颈动脉瘤的长期效果令人失望,再通和再治疗率较高。血流导向装置(PED)的血流导向治疗最近已被用作复杂动脉瘤的独立治疗方法,在有效性方面有显著改善,同时显示出与支架辅助线圈治疗相似的安全性。然而,关于其长期安全性和有效性的信息相对较少。在此,作者报告了在一项前瞻性队列研究中,使用 Pipeline 栓塞装置(PED)治疗的 107 例大型和巨型颈内动脉动脉瘤患者的 3 年安全性和有效性,该研究纳入了 Uncoilable 或 Failed Aneurysms(PUFS)试验。
PUFS 试验是一项对 109 个动脉瘤进行 PED 治疗的 107 例患者的前瞻性研究。主要有效性和安全性终点基于独立监测的 180 天临床和血管造影数据进行评估。患者按照长期随访方案进行随访,包括 1、3 和 5 年的临床和影像学随访。在本文中,作者报告了中期(3 年)的有效性和安全性数据。
在治疗后 3 年,76 个动脉瘤中有 74 个按照方案要求进行了导管血管造影。总体而言,76 个动脉瘤中有 71 个完全闭塞(完全闭塞率为 93.4%)。5 个动脉瘤因未闭塞而再次接受治疗,包括线圈或额外的 PED,其中 3 个在 3 年随访时得到治愈。因此,单纯使用 Pipeline 栓塞治疗 1 或 2 次的血管造影治愈率为 92.1%。在 3 年的血管造影中,未发现先前完全闭塞的动脉瘤再通。有 3 例(2.6%)为延迟的器械或动脉瘤相关的严重不良事件,均未导致永久性神经后遗症。在治疗后 6 个月至 3 年期间,未观察到任何迟发性出血性或缺血性脑血管事件或神经死亡。在 103 例存活患者中,85 例进行了功能预后评估,其中 80 例改良 Rankin 量表评分为 0-1。
血流导向装置在治疗颅内颈内动脉复杂的大、巨型动脉瘤中是安全有效的。与更传统的血管内治疗方法不同,血流导向治疗可导致血管进行性重塑,从而在更长时间的随访中导致完全闭塞动脉瘤消失,而不会发生延迟的动脉瘤再通和/或生长。临床试验注册号:NCT00777088(clinicaltrials.gov)。