Geometrical Analysis and Initial Experience With Bentley's BeFlared Bridging Stent for Fenestrated Endovascular Aneurysm Repair.

IF 1.8 2区 医学 Q3 PERIPHERAL VASCULAR DISEASE
Journal of Endovascular Therapy Pub Date : 2026-10-01 Epub Date: 2025-10-30 DOI:10.1177/15266028251385460
Gian Franco Veraldi, Lorenzo Grosso, Marco Macrì, Mario D'Oria, Sandro Lepidi, Gabriele Piffaretti, Luca Mezzetto
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引用次数: 0

Abstract

Introduction: Endovascular treatment of juxtarenal aortic aneurysms is now widely accepted as a safe and effective alternative to open repair. Bridging stent-grafts (BSGs) are used to provide continuity between the main aortic graft and renovisceral target vessels (TVs) in fenestrated endovascular aneurysm repair (FEVAR). The BeFlared (Bentley InnoMed GmbH, Hechingen, Germany) represents the first dedicated BSG specifically designed for FEVAR, incorporating a novel flaring system that enables precise positioning and sealing in a single step. This study aims to evaluate the impact of BeFlared on procedural efficiency, radiation exposure, and deployment accuracy.

Methods: A prospective registry of patients who underwent elective FEVAR at 3 Italian centers during February and March 2025 was retrospectively reviewed. Procedural parameters, including mean operative time, mean bridging time, and fluoroscopy duration, were recorded. Technical success was defined as successful stent deployment in all intended TVs. Cone-beam computed tomography (CBCT) was performed intraoperatively, and follow-up computed tomography angiography (CTA) was conducted 1 month post-procedure to assess geometric outcomes and complications. These parameters were compared with corresponding measurements obtained from a control cohort of patients who underwent FEVAR procedures, between 2020 and 2024 in the same 3 Italian centers, utilizing the Bentley BeGraft as BSG.

Results: Eight FEVAR procedures were performed, with a total of 31 TVs treated using BeFlared stents. The control cohort comprised 60 FEVAR procedures performed using the Bentley BeGraft as the BSG, involving a total of 185 renovisceral TVs. The BeFlared group demonstrated significantly improved intraoperative outcomes compared with the control group. Median operative time was 241 (interquartile range [IQR]=185-295) minutes vs 270.3 (IQR=207-365) minutes (p=0.022), mean bridging stent deployment time was 5 (IQR=4.25-6.15) minutes vs 7.6 (IQR=4.8-9.7) minutes (p<0.001), and median fluoroscopy time was 72.2 (IQR=51-81) minutes vs 82.7 (IQR=49.5-113) minutes (p=0.064). Only 1 patient in the BeFlared cohort required brief intensive care unit admission. The average hospital stay was 5.1 (IQR=4-6) days compared with 5.7 (3-10) days in the control group (p=0.882). In the BeFlared cohort, technical success was achieved in 96.7% of TVs (30/31), no perioperative deaths or TV-related complications were observed. Geometric analysis showed that BeFlared stents had more uniform deployment, with lower variability regarding the landing zone of the BSG in the TV (16.4 mm, IQR=16-17.1 vs 15.4 mm, IQR=14.2-16.6; p<0.001) and BSG aortic protrusion (4.2 mm, IQR=4.1-4.4 vs 5.1 mm, IQR=4.2-5.7; p<0.001) compared with BeGraft. BeFlared also demonstrated a significantly larger proximal stent diameter (10.6 mm, IQR=10.4-11.4 vs 99.5 mm, IQR=8.7-10.2; p<0.001), greater mean flaring angle (51.9 mm, IQR=47.4-55.8 vs 41.4 mm, IQR=37-48.3; p<0.001), and reduced inferior flaring angle (67.8 mm, IQR=61.5-72.4 vs 75.1 mm, IQR=67.4-82; p<0.001).

Conclusions: BeFlared demonstrated favorable short-term outcomes, with notable reductions in operative time, radiation exposure, and device manipulation. The geometric consistency and standardized deployment process offer encouraging early evidence of the system's clinical utility. Further studies are required in order to assess long-term safety and cost-effectiveness, as well as durability, across a wider patient population.Clinical ImpactThe BeFlared bridging stent introduces an innovative one-step flaring system that simplifies target vessel stenting during fenestrated endovascular aortic repair (FEVAR). This device enables more precise and reproducible deployment, reducing operative and fluoroscopy times while minimizing radiation exposure. For clinicians, these improvements translate into a safer, more standardized procedure with fewer technical maneuvers and potentially lower complication risks. The enhanced geometric consistency observed with BeFlared may improve long-term branch stability and durability, supporting its role as a next-generation device for complex aortic repair and a valuable advancement in endovascular practice.

Bentley桥式支架在开窗血管内动脉瘤修复中的几何分析及初步经验。
血管内治疗动脉瘤是目前公认的一种安全有效的开放性修复方法。在开窗血管内动脉瘤修复(FEVAR)中,桥式支架移植物(BSGs)用于提供主主动脉移植物和肾脏靶血管(TVs)之间的连续性。be喇叭口(Bentley InnoMed GmbH, Hechingen, Germany)是第一款专门为FEVAR设计的专用喇叭口,采用了一种新颖的喇叭口系统,可以在一个步骤中实现精确定位和密封。本研究旨在评估be喇叭声对程序效率、辐射暴露和部署准确性的影响。方法:回顾性分析2025年2月至3月在意大利3个中心接受选择性FEVAR的前瞻性登记患者。记录手术参数,包括平均手术时间、平均桥接时间和透视时间。技术上的成功被定义为在所有预期的电视中成功部署支架。术中进行锥形束计算机断层扫描(CBCT),术后1个月随访计算机断层血管造影(CTA)评估几何结果和并发症。这些参数与2020年至2024年间在意大利同一3个中心接受FEVAR手术的患者对照队列的相应测量结果进行比较,使用Bentley BeGraft作为BSG。结果:共进行了8次FEVAR手术,使用be喇角支架治疗了31例TVs。对照组包括60例FEVAR手术,使用Bentley BeGraft作为BSG,共185例肾脏电视。与对照组相比,be喇叭灯组术中疗效显著改善。中位手术时间为241(四分位间距[IQR]=185-295)分钟vs 270.3 (IQR=207-365)分钟(p=0.022),平均架桥支架部署时间为5 (IQR=4.25-6.15)分钟vs 7.6 (IQR=4.8-9.7)分钟(p结论:befraret显示出良好的短期效果,手术时间、辐射暴露和设备操作显著减少。几何一致性和标准化部署过程为该系统的临床应用提供了令人鼓舞的早期证据。为了在更广泛的患者群体中评估长期安全性和成本效益以及耐久性,需要进一步的研究。be喇叭形桥式支架引入了一种创新的一步扩口系统,简化了开窗血管内主动脉修复(FEVAR)过程中的靶血管支架置入。该设备可实现更精确和可重复的部署,减少手术和透视时间,同时最大限度地减少辐射暴露。对于临床医生来说,这些改进转化为更安全、更标准化的程序,技术操作更少,潜在的并发症风险更低。be喇叭声增强的几何一致性可以提高分支的长期稳定性和耐久性,支持其作为复杂主动脉修复的下一代设备的作用,并在血管内实践中取得了有价值的进步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.30
自引率
15.40%
发文量
203
审稿时长
6-12 weeks
期刊介绍: The Journal of Endovascular Therapy (formerly the Journal of Endovascular Surgery) was established in 1994 as a forum for all physicians, scientists, and allied healthcare professionals who are engaged or interested in peripheral endovascular techniques and technology. An official publication of the International Society of Endovascular Specialists (ISEVS), the Journal of Endovascular Therapy publishes peer-reviewed articles of interest to clinicians and researchers in the field of peripheral endovascular interventions.
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