School of Biomedical Engineering and Imaging Science, St Thomas' Hospital, King's College London, London, UK.
Vascular Surgery, CHU Grenoble, Grenoble, France.
J Endovasc Ther. 2023 Aug;30(4):592-599. doi: 10.1177/15266028221091894. Epub 2022 Apr 26.
Fenestrated endovascular aneurysm repair (fEVAR) is established for the treatment of juxtarenal, pararenal, and thoracoabdominal aortic aneurysms (TAAAs). Bridging stents are used to connect the main body of the stent graft to the aortic branch vessels. Complications related to the bridging stents compromise the durability of the repair and require urgent re-intervention. Here we present the midterm results of the BeGraft stent graft system used for fEVAR.
All consecutive patients treated with fEVAR and the current BeGraft Peripheral Stent Graft between November 2015 and September 2016 were included.
Thirty-nine consecutive patients (38 men) were enrolled and 101 BeGraft second-generation stent grafts were implanted. The median aneurysm diameter was 60 mm (54.5-67.0 mm). Aneurysms were juxtarenal and pararenal (19/39, 48.1%), type 4 TAAA (3/39, 7.7%), type 1, 2, and 3 TAAA (7/39, 17.8%), type 5 TAAA (4/39, 10.2%), and 15.4% (6/39) had a type I endoleak following a previous EVAR. Fifty-five BeGrafts were implanted in mesenteric arteries (22 in coeliac trunks, 31 in the superior mesenteric artery, and 2 in a hepatic or splenic artery) and 46 into renal arteries (24 right and 22 left). The renal artery diameters were 5, 6, 7, and 8 mm in 9, 7, 26, and 4 patients, respectively. Mesenteric arteries were exclusively stented with 9 and 10 mm diameter devices. The median follow-up was 33 months (IQ25 17-IQ75 36). During follow-up, 11 patients died (28%) from non-aneurysm-related causes. The overall patency rates for bridging stents were 98% and 97% at 1 and 2 years, respectively, with a freedom from secondary procedure rate on BeGraft stent grafts of 96% (97/101). All events occurred on stents implanted in renal arteries.
Early favorable outcomes are confirmed during longer term follow-up. Vigilant surveillance is required.
腔内分支型血管重建术(fEVAR)已被确立用于治疗肾周、肾旁和胸腹主动脉瘤(TAAAs)。桥接支架用于将支架移植物的主体连接到主动脉分支血管。与桥接支架相关的并发症会影响修复的耐久性,需要紧急再次介入治疗。在此,我们介绍了 BeGraft 支架移植物系统在 fEVAR 中的中期结果。
纳入 2015 年 11 月至 2016 年 9 月期间接受 fEVAR 和当前 BeGraft 外周支架移植物治疗的所有连续患者。
共纳入 39 例连续患者(38 例男性),共植入 101 枚 BeGraft 第二代支架移植物。中位动脉瘤直径为 60mm(54.5-67.0mm)。动脉瘤为肾周和肾旁(19/39,48.1%)、4 型 TAAA(3/39,7.7%)、1 型、2 型和 3 型 TAAA(7/39,17.8%)、5 型 TAAA(4/39,10.2%),15.4%(6/39)在先前的 EVAR 后出现 I 型内漏。55 枚 BeGraft 支架植入肠系膜动脉(22 枚在腹腔干,31 枚在肠系膜上动脉,2 枚在肝或脾动脉),46 枚植入肾动脉(24 枚右侧,22 枚左侧)。肾动脉直径分别为 9 例、7 例、26 例和 4 例患者的 5、6、7 和 8mm。肠系膜动脉仅用 9mm 和 10mm 直径的器械进行支架置入。中位随访时间为 33 个月(IQR25:17-IQR75:36)。随访期间,11 例患者(28%)死于非动脉瘤相关原因。桥接支架的总体通畅率分别为 1 年和 2 年时的 98%和 97%,BeGraft 支架移植物的无再次手术率为 96%(97/101)。所有事件均发生在植入肾动脉的支架上。
在更长的随访期间,证实了早期的良好结果。需要进行严密的监测。