Operative and 1-Year Outcomes of the Custom-Made Fenestrated Anaconda Aortic Stent Graft-A UK Multicenter Study

被引:13
作者
Colgan, Frances E. [1 ]
Bungay, Peter M. [2 ]
Burfitt, Nicholas [3 ]
Hatrick, Andrew [4 ]
Clarke, Michael J. [1 ]
Davies, Alun H. [3 ]
Jenkins, Michael [3 ]
Gerrard, David [4 ]
Quarmby, John W. [2 ]
Williams, Robin [1 ]
机构
[1] Newcastle Upon Tyne Hosp NHS Trust, Freeman Hosp, Northern Vasc Ctr, Freeman Rd, Newcastle Upon Tyne NE7 7ER, Tyne & Wear, England
[2] Royal Derby Hosp, Dept Vasc Surg & Intervent Radiol, Derby, England
[3] Imperial Coll Healthcare NHS Trust, Dept Vasc Surg & Intervent Radiol, London, England
[4] Frimley Pk Hosp NHS Fdn Trust, Dept Vasc Surg & Intervent Radiol, Frimley, Surrey, England
关键词
ENDOVASCULAR-ANEURYSM-REPAIR; EXPERIENCE; VARIABILITY; COMPLEX; SYSTEM;
D O I
10.1016/j.avsg.2017.05.027
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Early and 1-year outcomes are presented for fenestrated endovascular aneurysm repair (FEVAR) of complex aortic aneurysmal disease with the custom-made Anaconda fenestrated stent graft in 101 patients. Methods: Retrospective site-reported data from the first 101 elective cases (2010-2014) from 4 UK centers were studied to evaluate patient demographics, aneurysm morphology, clinical success, and 1-year outcomes in patients undergoing fenestrated aneurysm repair with the custom-made Anaconda device. Results: 101 fenestrated grafts (median age 76, 85% male) were implanted with a total of 255 fenestrations (196 renal arteries, 48 superior mesenteric artery, and 11 celiac arteries) with 3% mortality, 98.4% target vessel patency (TVP) at 30 day follow-up. Although 15 type I or III endoleaks were demonstrated at completion angiography, all 10 type Ia endoleaks resolved spontaneously. Survival by Kaplan-Meier analysis was 97% and 91% at 1 month and 1 year, respectively; with 75.8% showing reduction in abdominal aortic aneurysm diameter and only 1 patient with sac expansion. Freedom from loss of TVP was 97.6%. Conclusions: Custom-made fenestrated Anaconda devices demonstrate low procedural mortality and a high rate of technical and clinical success at 30 days and 1 year.
引用
收藏
页码:257 / 264
页数:8
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