Department of Neurosurgery, State University of New York at Stony Brook, Stony Brook, New York 11794-8122, USA.
J Neurointerv Surg. 2010 Mar;2(1):16-22. doi: 10.1136/jnis.2009.000521. Epub 2009 Sep 15.
This report details experience with the Neuroform stent, with an emphasis on evolving treatment strategies, complication rates and treatment durability.
All patients undergoing Neuroform stent assisted aneurysm treatment were registered in prospectively maintained endovascular databases at two institutions.
284 patients with 302 aneurysms underwent aneurysm treatment with Neuroform during a 42-month study period. Imaging follow-up was available for 166 of 286 saccular aneurysms which were treated with stents and coils (average interval 12.9 months). 80 demonstrated progressive thrombosis (48.2%), 40 were unchanged (24.1%) and 46 (27.7%) demonstrated re-canalization, 25 (15.1%) of which were major recanalizations requiring retreatment. The vast majority of recanalizations and retreatments were observed in large or giant aneurysms. A cumulative total of 25 ischemic strokes (8.8%) and eight neurovascular deaths (2.8%) were recorded in these patients. Ten of these strokes were associated with transient deficits which went on to complete resolution by the time of discharge or at the initial clinical follow-up, yielding a significant stroke rate of 5.3%. Delayed (>48 h) complications, including four deaths-related to stroke (n=2, 6 days and 8 weeks post-procedure) and spontaneous parenchymal hemorrhages (n=2)-represent events which are a direct consequence of stenting and likely would not have been encountered in the context of standard non-stent supported embolization techniques.
Neuroform facilitates the endovascular treatment of complex and wide necked cerebral aneurysms. However, complete occlusion at angiographic follow-up remains uncommon and is observed in only one-third of patients. Delayed complications (>48 h) represent an important component of the overall complications associated with Neuroform assisted aneurysm embolization.
本报告详细介绍了 Neuroform 支架的使用经验,重点介绍了不断发展的治疗策略、并发症发生率和治疗持久性。
在两个机构的前瞻性维护的血管内数据库中注册了所有接受 Neuroform 支架辅助治疗的动脉瘤患者。
在 42 个月的研究期间,284 名患者的 302 个动脉瘤接受了 Neuroform 治疗。对 286 个囊状动脉瘤中的 166 个进行了影像学随访,这些动脉瘤接受了支架和线圈治疗(平均间隔时间为 12.9 个月)。80 个显示进行性血栓形成(48.2%),40 个未改变(24.1%),46 个(27.7%)显示再通,其中 25 个(15.1%)需要再次治疗。再通和再次治疗的绝大多数发生在大或巨大动脉瘤中。在这些患者中记录了 25 例缺血性中风(8.8%)和 8 例神经血管死亡(2.8%)。其中 10 例中风与短暂性缺陷有关,在出院时或首次临床随访时完全缓解,因此,显著的中风发生率为 5.3%。迟发性(>48 小时)并发症,包括 4 例与中风相关的死亡(n=2,术后 6 天和 8 周)和自发性实质内出血(n=2),是支架直接导致的事件,在标准的非支架支持栓塞技术的情况下不会发生。
Neuroform 有助于复杂和宽颈脑动脉瘤的血管内治疗。然而,在血管造影随访中完全闭塞仍然不常见,仅在三分之一的患者中观察到。迟发性并发症(>48 小时)是与 Neuroform 辅助动脉瘤栓塞相关的总体并发症的重要组成部分。