Hellstern Victoria, Aguilar-Pérez Marta, Henkes Elina, Serna-Candel Carmen, Wendl Christina, Bäzner Hansjörg, Ganslandt Oliver, Henkes Hans
Neuroradiologische Klinik, Kopf- und Neurozentrum, Klinikum Stuttgart, Stuttgart, Germany.
Institut für Röntgendiagnostik, Zentrum für Neuroradiologie, Universitätsklinikum Regensburg, Regensburg, Germany.
Front Neurol. 2021 Jul 16;12:711863. doi: 10.3389/fneur.2021.711863. eCollection 2021.
Flow diverter (FD) stents have become one of the most common tools for treating intracranial aneurysms; however, their role in treating posterior circulation aneurysms is still discussed with controversy. In this study, we evaluated the safety and effectiveness of p64 FD for the treatment of saccular, unruptured aneurysms in the posterior circulation over a long-term follow-up period in a single center. From our prospectively maintained database, we retrospectively identified patients who underwent treatment of an intracranial saccular aneurysm arising from the posterior circulation with ≥1 p64 FD implanted or attempted between October 2012 and December 2019. Aneurysms could have been treated with prior or concomitant saccular treatment (e.g., coiling, intra-aneurysmal flow diversion). Aneurysms with parent vessel implants other than p64, fusiform aneurysms, and dissections were excluded. Peri- and postprocedural complications, clinical outcome, and clinical and angiographic follow-up results were evaluated. In total, 54 patients (45 female, 9 male; mean age 55.1 years) with 54 intracranial aneurysms met the inclusion criteria. In 51 cases (94.4%), one p64 was implanted; in 2 cases (3.7 %), two p64s were implanted; in one case, deployment of the p64 was not feasible. Procedural complications occurred in 3.7% and postprocedural complications in 9.3 %, respectively. Hemorrhagic complications occurred in 2/54 patients (3.7%), thereof one fatal parenchymal hemorrhage. Ischemic complications were observed in 5/54 patients (9.3%). Early, mid-term, and long-term angiographic follow-up examinations showed complete or near-complete aneurysm occlusion, defined according to the O'Kelly -Marotta (OKM) scale as OKM C + D in 56, 75.6, and 82.9 %, respectively. Asymptomatic side vessel occlusions occurred in 3.8%, each during the first follow-up. The implantation of a p64 FD is a safe and effective device for endovascular treatment of posterior circulation saccular aneurysms with a high success rate and low morbi-mortality.
血流导向(FD)支架已成为治疗颅内动脉瘤最常用的工具之一;然而,其在治疗后循环动脉瘤中的作用仍存在争议。在本研究中,我们评估了p64 FD在单中心长期随访期间治疗后循环囊状未破裂动脉瘤的安全性和有效性。从我们前瞻性维护的数据库中,我们回顾性地确定了2012年10月至2019年12月期间接受过≥1枚p64 FD植入或尝试植入治疗后循环颅内囊状动脉瘤的患者。动脉瘤可能已接受过先前或同期的囊状治疗(如栓塞、瘤内血流导向)。排除了除p64以外有载瘤血管植入物的动脉瘤、梭形动脉瘤和夹层动脉瘤。评估围手术期和术后并发症、临床结局以及临床和血管造影随访结果。共有54例患者(45例女性,9例男性;平均年龄55.1岁)的54个颅内动脉瘤符合纳入标准。51例(94.4%)植入了1枚p64;2例(3.7%)植入了2枚p64;1例中,p64的部署不可行。手术并发症发生率为3.7%,术后并发症发生率为9.3%。出血性并发症发生在2/54例患者(3.7%)中,其中1例为致命性脑实质出血。5/54例患者(9.3%)观察到缺血性并发症。早期、中期和长期血管造影随访检查显示,根据奥凯利-马罗塔(OKM)量表定义,动脉瘤完全或近乎完全闭塞,分别为56%、75.6%和82.9%。无症状侧支血管闭塞发生率为3.8%,均发生在首次随访期间。p64 FD植入术是一种安全有效的血管内治疗后循环囊状动脉瘤的装置,成功率高,病死率和致残率低。