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腔内动脉瘤封堵联合平行移植物治疗复杂腹主动脉瘤的早期经验:ASCEND 注册研究。

Early Experience With Endovascular Aneurysm Sealing in Combination With Parallel Grafts for the Treatment of Complex Abdominal Aneurysms: The ASCEND Registry.

机构信息

1 St Georges Vascular Institute, London, UK.

2 Department of Vascular Surgery, University Hospital, Mainz, Germany.

出版信息

J Endovasc Ther. 2017 Dec;24(6):764-772. doi: 10.1177/1526602817731103. Epub 2017 Sep 12.

Abstract

PURPOSE

To report the results of the ASCEND Registry of cases involving endovascular aneurysm sealing (EVAS) in combination with chimney grafts (chEVAS) for the treatment of para- and juxtarenal aortic aneurysms (AAA).

METHODS

A retrospective, multicenter registry established in 8 vascular centers between 2013 and 2016 recorded the treatment results and follow-up of chEVAS procedures for nonruptured AAAs; data were analyzed using standardized outcome measures. In the observation period, 154 patients (mean age 72.3±7.7 years; 124 men) underwent elective treatment for de novo juxtarenal and pararenal aneurysms and formed the study group.

RESULTS

Sixty-two (40.3%) of the cohort were treated using a single parallel graft, 54 (35.1%) with double chimneys, 27 (17.5%) with triple chimneys, and 11 (7.1%) with 4 chimneys. The 30-day mortality was 2.8%, and there were 4 perioperative strokes (1 fatal). At 1 year, the freedom from all-cause mortality was 89.8% and the freedom from aneurysm-related mortality was 94.3%. There were 3 endoleaks within 90 days of the procedure, one type Ia and 2 type Ib. The freedom from type Ia endoleaks was 95.7% at 1 year. There were no types II or III endoleaks in this series; the freedom from all endoleaks was 94.2% at 1 year. Freedom from reintervention at 1 year was 89.2%. Target vessel patency rates at 1 year were 97.7%, 99.3%, 100%, and 100% for the left renal, right renal, superior mesenteric artery, and celiac axis stents, respectively.

CONCLUSION

The ASCEND Registry supports a proof of concept for the use of polymer technology and EVAS with parallel grafts in managing patients with complex aortic disease. The future role of chEVAS will be defined by studies that assess mid- to long-term durability.

摘要

目的

报告涉及血管腔内动脉瘤密封(EVAS)联合烟囱移植物(chEVAS)治疗内脏和肾旁主动脉瘤(AAA)的 ASCEND 登记处的结果。

方法

该回顾性、多中心登记处于 2013 年至 2016 年在 8 个血管中心建立,记录了非破裂性 AAA 的 chEVAS 治疗结果和随访数据;使用标准化的结局指标进行分析。在观察期内,154 名患者(平均年龄 72.3±7.7 岁;124 名男性)因新发肾旁和内脏动脉瘤接受择期治疗,构成研究组。

结果

队列中有 62 例(40.3%)采用单一平行移植物治疗,54 例(35.1%)采用双烟囱,27 例(17.5%)采用三烟囱,11 例(7.1%)采用四烟囱。30 天死亡率为 2.8%,围手术期有 4 例卒中(1 例死亡)。1 年时,全因死亡率的无事件生存率为 89.8%,动脉瘤相关死亡率的无事件生存率为 94.3%。术后 90 天内有 3 例内漏,1 型 Ia 漏和 2 型 Ib 漏。1 年时,Ia 型内漏的无事件生存率为 95.7%。本系列无 II 型或 III 型内漏,1 年时所有内漏的无事件生存率为 94.2%。1 年时无再次干预的无事件生存率为 89.2%。1 年时左肾、右肾、肠系膜上动脉和腹腔干支架的靶血管通畅率分别为 97.7%、99.3%、100%和 100%。

结论

ASCEND 登记处支持在治疗复杂主动脉疾病患者时使用聚合物技术和 EVAS 联合平行移植物的概念验证。chEVAS 的未来作用将由评估中至长期耐久性的研究来确定。

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