E-054 pulserider辅助治疗颅内动脉瘤的研究

R. de Leacy, A. Puri, R. Starke, B. Jankowitz, A. Yoo, F. Gariel, S. Jahshan, Z. Kulcsár, C. Schirmer, C. Chivot, J. Howington, G. Pero, T. Yao, A. Polifka, A. Evans, O. Zaidat
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Primary outcome measures were core-lab assessed modified Raymond-Roy (mRR) occlusion at final procedural angiogram, and where available, at 6 months (+/-3 months) or 1 year (COVID allowed window: -3 months/+1.5 years). Safety outcomes were procedureand device-related adverse events. Results Seventeen subjects (mean age 64.4 ± 8.69 years, 12 female) were treated with the PulseRider device. All cases were unruptured and two were retreatments of previously coiled aneurysms. All aneurysms had saccular morphology, 14/ 15 (93.3%) were wide neck and 13/15 (86.7%) were at a bifurcation. Target aneurysm locations included basilar artery (6/15, 40.0%), MCA bifurcation (4/15, 26.7%), ACA (3/15, 20%), ICA terminus (1/15, 6.7%), and M2 (distal to bifurcation, 1/15, 6.7%), with a mean parent vessel diameter of 2.65 ± 0.440mm. PulseRider was successfully implanted with the ability to retain the coil mass in all cases. Mean packing density was 29.7 ± 11.32%. Adequate occlusion (mRR I or II) was achieved in 86.7% (13/15) cases immediately post procedure, 100% (3/3) at 6 moths, and 75% (3/4) at 1 year. There were no intraprocedural ruptures, no symptomatic thromboembolic events, and no device related SAEs through the maximum follow up. 87.5% (7/8) subjects had mRS 0-2 at 1 year. There were no aneurysm retreatments. 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引用次数: 0

摘要

PulseRider (Cerenovus, Irvine, CA)是一种辅助颈部桥接装置,旨在帮助卷曲宽颈分岔颅内动脉瘤。我们介绍了PulseRider辅助线圈栓塞脑动脉瘤在常规临床实践中的结果,包括在STERLING注册表中。STERLING (NCT03642639)是一项使用Galaxy和microframe线圈(Cerenovus, Irvine, CA)进行颅内动脉瘤血管内治疗的前瞻性全球注册研究。来自STERLING的PulseRider病例包括在这个中期分析中。主要结局指标是在最终手术血管造影时进行核心实验室评估的改良雷蒙德-罗伊(mRR)闭塞,如果有的话,在6个月(+/-3个月)或1年(COVID允许窗口:-3个月/+1.5年)。安全性结果是手术和器械相关的不良事件。结果17例患者(平均年龄64.4±8.69岁,女性12例)采用PulseRider装置治疗。所有病例均未破裂,其中2例为先前卷曲动脉瘤的再治疗。所有动脉瘤均呈囊状形态,宽颈14/ 15(93.3%),分岔13/15(86.7%)。靶动脉瘤位置包括基底动脉(6/15,40.0%)、MCA分叉(4/15,26.7%)、ACA(3/15, 20%)、ICA末端(1/15,6.7%)、M2(分叉远端,1/15,6.7%),平均母血管直径2.65±0.40 mm。在所有病例中,PulseRider都成功植入并保留了线圈的质量。平均堆积密度为29.7±11.32%。86.7%(13/15)的病例术后立即达到了足够的闭塞(mRR I或II), 100%(3/3)的病例术后6个月达到,75%(3/4)的病例术后1年达到。通过最大的随访,没有术中破裂,没有症状性血栓栓塞事件,没有器械相关的SAEs。87.5%(7/8)的受试者1年时mRS为0-2。没有动脉瘤再治疗。结论:在这项正在进行的STERLING登记的中期分析中,使用PulseRider装置联合使用Galaxy和microframe线圈栓塞治疗颅内动脉瘤显示出良好的安全性和高的充分闭塞率以及良好的临床结果。
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E-054 Pulserider-assisted treatment of intracranial aneurysms in the sterling registry
Introduction PulseRider (Cerenovus, Irvine, CA) is an adjunctive neck bridging device designed to aid in coiling of wide neck bifurcation intracranial aneurysms. We present outcomes of PulseRider assisted coil embolization of brain aneurysms in routine clinical practice included in the STERLING registry. Materials and Methods STERLING (NCT03642639) is a prospective, global registry of endovascular treatment of intracranial aneurysms with Galaxy and MicrusFrame coils (Cerenovus, Irvine, CA). PulseRider cases from STERLING were included in this interim analysis. Primary outcome measures were core-lab assessed modified Raymond-Roy (mRR) occlusion at final procedural angiogram, and where available, at 6 months (+/-3 months) or 1 year (COVID allowed window: -3 months/+1.5 years). Safety outcomes were procedureand device-related adverse events. Results Seventeen subjects (mean age 64.4 ± 8.69 years, 12 female) were treated with the PulseRider device. All cases were unruptured and two were retreatments of previously coiled aneurysms. All aneurysms had saccular morphology, 14/ 15 (93.3%) were wide neck and 13/15 (86.7%) were at a bifurcation. Target aneurysm locations included basilar artery (6/15, 40.0%), MCA bifurcation (4/15, 26.7%), ACA (3/15, 20%), ICA terminus (1/15, 6.7%), and M2 (distal to bifurcation, 1/15, 6.7%), with a mean parent vessel diameter of 2.65 ± 0.440mm. PulseRider was successfully implanted with the ability to retain the coil mass in all cases. Mean packing density was 29.7 ± 11.32%. Adequate occlusion (mRR I or II) was achieved in 86.7% (13/15) cases immediately post procedure, 100% (3/3) at 6 moths, and 75% (3/4) at 1 year. There were no intraprocedural ruptures, no symptomatic thromboembolic events, and no device related SAEs through the maximum follow up. 87.5% (7/8) subjects had mRS 0-2 at 1 year. There were no aneurysm retreatments. Conclusion In this interim analysis of the ongoing STERLING registry, treatment of intracranial aneurysms with the PulseRider device in conjunction with embolization using Galaxy and MicrusFrame coils showed excellent safety outcomes and high rates of adequate occlusion and good clinical outcome.
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