German Aortic Center Hamburg, Department of Vascular Medicine, University Heart & Vascular Center, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
Department of Vascular and Endovascular Surgery, St. Franziskus Hospital / University of Münster, Germany.
J Endovasc Ther. 2020 Dec;27(6):910-916. doi: 10.1177/1526602820944611. Epub 2020 Aug 4.
To compare the outcomes of iliac branch devices (IBD) used in combination with standard endovascular aneurysm repair (EVAR) vs with fenestrated/branched EVAR (f/bEVAR) to treat complex aortoiliac aneurysms. The pELVIS Registry database containing the outcomes of IBD use at 8 European centers was interrogated to identify all IBD procedures that were combined with either standard EVAR or f/bEVAR. Among 669 patients extracted from the database, 629 (mean age 72.1±8.8 years; 597 men) had received an IBD combined with standard EVAR vs 40 (mean age 71.1±8.0 years; 40 men) who underwent f/bEVAR with an IBD. The mean aortic aneurysm diameters were 46.4±13.3 mm in the f/bEVAR patients vs 45.0±15.5 mm in the standard EVAR cases. The groups were similar in terms of baseline clinical characteristics and aneurysm morphology. The Kaplan-Meier method was used to compare patient survival, IBD occlusion, type III endoleak, and aneurysm-related reinterventions in follow-up. The estimates are presented with the 95% confidence interval (CI). Technical success was 100% in the f/bEVAR+IBD group and 99% in the EVAR+IBD group (p=0.85). The 30-day mortality was 0% vs 0.5%, respectively (p=0.66), while the 30-day reintervention rates were 7.5% vs 4.1% (p=0.31). The mean follow-up was 32.1±21.3 months for f/bEVAR+IBD patients (n=30) and 35.5±26.8 months for EVAR+IBD patients (n=571; p=0.41). The 12-month survival estimates were 93.4% (95% CI 93.2% to 93.6%) in the EVAR+IBD group vs 93.6% (95% CI 93.3% to 93.9%) for the f/bEVAR+IBD group (p=0.93). There were no occlusions or type III endoleaks in the f/bEVAR+IBD group at 12 months, while the estimates for freedom from occlusion and from type III endoleak in the EVAR+IBD group were 97% (95% CI 96.8% to 97.2%) and 98.5% (95% CI 98.4% to 98.6%), respectively. The 12-month estimates for freedom for aneurysm-related reintervention were 93% (95% CI 92.7% to 93.3%) in the EVAR+IBD group vs 86.4% (95% CI 85.9% to 86.9%) in the f/bEVAR+IBD patients (p=0.046). Treatment of complex aortoiliac disease with f/bEVAR+IBD can achieve equally good early and 1-year outcomes compared to treatment with IBDs and standard bifurcated stent-grafts, except for a somewhat higher reintervention rate in f/bEVAR patients.
比较髂分支装置(IBD)与标准血管内动脉瘤修复术(EVAR)联合应用与腔内修复术(f/bEVAR)治疗复杂主动脉-髂动脉瘤的结果。通过检索 8 个欧洲中心的 pELVIS 登记数据库,以确定所有与标准 EVAR 或 f/bEVAR 联合使用的 IBD 手术。从数据库中提取了 669 例患者,其中 629 例(平均年龄 72.1±8.8 岁;597 例男性)接受了与标准 EVAR 联合的 IBD,40 例(平均年龄 71.1±8.0 岁;40 例男性)接受了与 IBD 联合的 f/bEVAR。f/bEVAR 患者的平均主动脉瘤直径为 46.4±13.3mm,标准 EVAR 组为 45.0±15.5mm。两组在基线临床特征和动脉瘤形态方面相似。采用 Kaplan-Meier 法比较随访中患者的生存、IBD 闭塞、III 型内漏和与动脉瘤相关的再介入。结果用 95%置信区间(CI)表示。f/bEVAR+IBD 组的技术成功率为 100%,EVAR+IBD 组为 99%(p=0.85)。30 天死亡率分别为 0%和 0.5%(p=0.66),30 天再介入率分别为 7.5%和 4.1%(p=0.31)。f/bEVAR+IBD 患者的平均随访时间为 32.1±21.3 个月(n=30),EVAR+IBD 患者的平均随访时间为 35.5±26.8 个月(n=571;p=0.41)。EVAR+IBD 组的 12 个月生存率估计为 93.4%(95%CI 93.2%至 93.6%),f/bEVAR+IBD 组为 93.6%(95%CI 93.3%至 93.9%)(p=0.93)。f/bEVAR+IBD 组在 12 个月时无闭塞或 III 型内漏,而 EVAR+IBD 组无闭塞和 III 型内漏的估计分别为 97%(95%CI 96.8%至 97.2%)和 98.5%(95%CI 98.4%至 98.6%)。EVAR+IBD 组 12 个月时与动脉瘤相关的再介入的估计为 93%(95%CI 92.7%至 93.3%),f/bEVAR+IBD 患者为 86.4%(95%CI 85.9%至 86.9%)(p=0.046)。与使用 IBD 和标准分叉支架移植物治疗相比,f/bEVAR+IBD 治疗复杂主动脉-髂疾病可获得同样良好的早期和 1 年结果,除了 f/bEVAR 患者的再介入率略高外。