Four‐Year Follow‐Up on the First‐in‐Human Experience With Nautilus Intrasaccular System Assisted Coiling for Unruptured Intracranial Aneurysms

IF 2.1 Q3 CLINICAL NEUROLOGY
N. Sakai, Shuhei Kawabata, Takayuki Funatsu, Tomohiro Okuda, R. Akiyama, Mikiya Beppu, Y. Matsui, Hiromasa Adachi, K. Horiuchi, H. Imamura, C. Sakai, S. Tani, H. Adachi, N. Sasaki, Soji Tokunaga, R. Fukumitsu, T. Shigematsu
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Abstract

The authors present the long‐term (4 year) results of a first‐in‐man, single‐center case series with the Nautilus Intrasaccular System for the embolization of wide‐neck intracranial aneurysms. From February 2018 to July 2018, the authors enrolled 5 patients into a first‐in‐human study of the Nautilus device. After treatment, patients underwent 6 months with digital subtraction angiography and 3 years with magnetic resonance angiography according to institutional standard of care. Occlusion rates were core‐laboratory adjudicated for the digital subtraction angiography and independently assessed by a neurointerventionalist not part of the care team for the magnetic resonance angiography. Neurological outcome (modified Ranking scale score) was evaluated at 24 hours, 7 days, 6 months, and 1, 2, 3, and 4 years, and adverse events were collected during the first 6 months post treatment. Five patients with unruptured, wide‐necked aneurysms were treated and followed up for 4 years. Aneurysm locations included basilar bifurcation (2 of 5), internal carotid artery terminus (1 of 5), superior cerebellar artery (1 of 5), and the anterior communicating artery (1 of 5). The average aneurysm size was 7.6 mm and the average neck diameter was 5.2 mm. Immediate complete and near‐complete occlusion (Raymond–Roy classification class I and II) was achieved in 80% (4 of 5) of the aneurysms. Occlusion results improved at 6 months and remained stable at 3 years, without retreatment (Raymond–Roy classification class I 80%, class I and II 100%). All patients maintained good neurological outcome at all follow‐ups (modified Ranking scale 0). This initial clinical experience provides early evidence of the long‐term safety and effectiveness of the new intrasaccular neck bridging device, Nautilus. The Nautilus appears to add a simple, safe, and effective option and solution to the coil embolization of the wide‐neck aneurysm.
鹦鹉螺囊内系统辅助卷绕术治疗颅内未破裂动脉瘤的临床研究
作者介绍了Nautilus球囊内系统用于宽颈颅内动脉瘤栓塞的首次单中心病例系列的长期(4年)结果。从2018年2月到2018年7月,作者招募了5名患者参与Nautilus装置的首次人体研究。治疗后,根据机构护理标准,患者接受了6个月的数字减影血管造影和3年的磁共振血管造影。闭塞率由数字减影血管造影术的核心实验室裁定,并由非磁共振血管造影学护理团队成员的神经干预学家独立评估。在第24小时、第7天、第6个月、第1年、第2年、第3年和第4年评估神经系统结果(改良排名量表评分),并在治疗后的前6个月收集不良事件。对5例未破裂的宽颈动脉瘤患者进行了治疗并随访4年。动脉瘤的位置包括基底分叉(2/5)、颈内动脉末端(1/5)、小脑上动脉(1/5。平均动脉瘤大小为7.6 mm,平均颈部直径为5.2 mm。80%(4/5)的动脉瘤实现了即时完全和近完全闭塞(Raymond–Roy分类I级和II级)。闭塞结果在6个月时有所改善,在3年时保持稳定,没有再治疗(Raymond–Roy分类I类80%,I和II类100%)。所有患者在所有随访中都保持了良好的神经系统结果(改良的排名量表0)。这一初步临床经验为新型伏内颈桥装置Nautilus的长期安全性和有效性提供了早期证据。Nautilus似乎为宽颈动脉瘤的线圈栓塞增加了一种简单、安全、有效的选择和解决方案。
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