Vascular Surgery, University Hospital of Verona, University of Verona School of Medicine, Verona, Italy.
Vascular Surgery, NOCSAE Nuovo Ospedale Civile di Baggiovara Sant'Agostino Estense, Baggiovara, Modena, Italy.
J Endovasc Ther. 2021 Aug;28(4):575-584. doi: 10.1177/15266028211012403. Epub 2021 May 11.
To report preliminary outcomes of Viabahn Balloon-Expandable Endoprosthesis (VBX) stent-graft as bridging stent for renal arteries in fenestrated endovascular aneurysm repair (FEVAR).
Between 2018 and 2019, patients undergoing FEVAR at 3 referral Italian university hospitals were prospectively collected. During the study period, VBX was the first-line choice as bridging stent for renal arteries. Procedural and anatomical data were analyzed, including renal artery (RA) configuration. A dedicated software (3Mensio, Vascular Imaging, Bilthoeven, The Netherlands) was used and RA anatomy classified as follow: upward-oriented in case of any angle >30° above the horizontal or transverse axis perpendicular to the aortic axis, downward-oriented if there was an angle >30° measured below the transverse axis and downward + upward in case of an angle <30° associated with a renal artery angulation >90°. Primary endpoints were technical success, defined as complete deployment of the fenestrated endograft without target vessel (TV) loss, limb stenosis or occlusion and type I or III endoleak, and freedom from target artery instability (TAI), defined by target vessel-related death, occlusion, rupture or reintervention for stenosis, endoleak or disconnection. Secondary endpoints were target artery patency rate and freedom from reinterventions.
A total of 26 elective FEVAR for juxta/pararenal aneurysm (20), thoracoabdominal type II (3) and type IV (3) were included. Fifty-one RA were planned for revascularization. Of these, 32 were downward, 10 horizontal, 6 upward, 4 were downward + upward. Technical success was achieved in 88.5% (23/26) of patients and 94.2% (48/51) of the TVs. One occlusion (2.1%) occurred within 30 days in a patient with previous endovascular aortic repair and suprarenal fixation. During follow-up (median 10 months), there was 1 type IC endoleak after 6 months (2.1%) in a patient with upward plus downward arterial orientation. Freedom from TAI was 96.1% (CI = 0.89 to 1.04) at first month and 92.3% (CI = 0.82 to 1.03) at 6 months. No aneurysm-related mortality and renal insufficiency occurred during follow-up.
The use of VBX as bridging stent of RA in FEVAR is safe and feasible. Previous EVAR and tortuosity of RA may be a challenging on target vessel fate.
报告 Viabahn 球囊扩张式覆膜支架(VBX)作为肾动脉分支支架在腔内血管重建治疗(FEVAR)中的初步结果。
2018 年至 2019 年,3 家意大利转诊大学医院前瞻性地收集了接受 FEVAR 的患者。在此期间,VBX 是肾动脉分支的首选支架。分析了包括肾动脉(RA)形态在内的手术和解剖数据。使用专用软件(3Mensio,血管成像,Bilthoeven,荷兰),将 RA 解剖分为以下几类:向上倾斜,如果与主动脉轴垂直的横轴上方有任何角度> 30°;向下倾斜,如果在横轴下方有角度> 30°;向下+向上倾斜,如果角度<30°,同时肾动脉有>90°的角度。主要终点为技术成功,定义为完全展开的覆膜支架,没有靶血管(TV)丢失、分支狭窄或闭塞以及 I 型或 III 型内漏;以及目标动脉稳定性(TAI)不受影响,定义为与靶血管相关的死亡、闭塞、破裂或因狭窄、内漏或分离而再次干预。次要终点为目标动脉通畅率和免于再次干预。
共纳入 26 例肾周/肾旁动脉瘤(20 例)、胸腹主动脉 II 型(3 例)和 IV 型(3 例)的选择性 FEVAR。计划对 51 个 RA 进行血运重建。其中,32 个向下,10 个水平,6 个向上,4 个向下+向上。26 例患者中,88.5%(23/26)和 51 个 TV 中,94.2%(48/51)达到技术成功。1 例患者(2.1%)在 30 天内发生闭塞,该患者此前曾接受过血管内主动脉修复和肾上固定术。在随访(中位时间 10 个月)期间,1 例患者(2.1%)在 6 个月时出现 IIC 型内漏,该患者的 RA 动脉呈向上加向下的倾斜。第 1 个月 TAI 无丢失率为 96.1%(CI = 0.89 至 1.04),第 6 个月为 92.3%(CI = 0.82 至 1.03)。在随访期间,没有发生与动脉瘤相关的死亡和肾功能不全。
在 FEVAR 中,使用 VBX 作为 RA 分支支架是安全可行的。先前的 EVAR 和 RA 的迂曲可能会对靶血管的命运构成挑战。