Reintervention Rate after Treatment with the INCRAFT AAA Ultra–Low-Profile Stent Graft System

IF 1.4 4区 医学 Q3 PERIPHERAL VASCULAR DISEASE
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引用次数: 0

Abstract

Background

The INCRAFT stent graft system is an ultra–low-profile endograft for the exclusion of infrarenal aortic aneurysms. In the market approval studies, an increased rate of device-related complications was observed and the endograft was approved with mandated postmarketing investigations. Our aim was to analyze mid-term outcomes of a real-world patient cohort treated with the INCRAFT endograft.

Methods

Consecutive patients treated with the INCRAFT endograft between February 2015 and December 2022 at a single institution were included. In accordance with the Society for Vascular Surgery reporting standards, safety endpoints were reported and outcome endpoints included reinterventions, technical success, aortic-related and overall-mortality, endoleak, stent fracture, and endograft migration >5 mm.

Results

Eighty patients (85% male) with a mean age of 76 ± 7 years were included. Fifty-two patients (65%) were treated within the endograft's instruction for use. Mean aortic diameter was 59 ± 10 mm and 91% of the procedures were performed percutaneously. Mean follow-up (FU) was 37 ± 25 months and there was no aortic- or procedure-related mortality. Reinterventions occurred in 25 patients (31%) with a freedom from reintervention at 1, 3, and 5 years of 84%, 66%, and 55%. The most frequent reinterventions were limb graft stenting (23%) and type II endoleak embolization (14%). Limb occlusion rate was 9% and in 3 patients (4%) distal endograft migrations >5 mm occurred. Persisting type II endoleaks were observed in 29% and aneurysm diameter was stable in 41% and had shrunk in 38%. Three type III endoleaks (4%) developed during FU and 4 open conversions (5%) were necessary. No known risk factors, including treatment outside instruction for use, were predictive for reinterventions.

Conclusions

Treatment of infrarenal aortic aneurysms with the INCRAFT stent graft system was safe and successful. Nevertheless, a substantial rate of reinterventions was necessary during FU to maintain endograft patency and prevent aneurysm growth.

使用 incraft aaa 超低剖面支架移植系统治疗后的再介入率。
目的:INCRAFT 支架移植系统是一种用于排除肾下主动脉瘤的超扁平内植物。在市场审批研究中,我们观察到与设备相关的并发症发生率有所上升,因此在批准该内移植物时强制要求进行上市后调查。我们的目的是分析使用 INCRAFT 内植物治疗的真实世界患者队列的中期疗效:方法:纳入2015年2月至2022年12月在一家机构接受INCRAFT内植物治疗的连续患者。根据血管外科学会的报告标准,报告了安全性终点,结果终点包括再介入、技术成功率、主动脉相关死亡率和总死亡率、内漏、支架断裂和内膜移位>5毫米:共纳入 80 名患者(85% 为男性),平均年龄为 76 ± 7 岁。52名患者(65%)在内膜移植物使用说明书(IFU)规定的范围内接受了治疗。平均主动脉直径为 59 ± 10 毫米,91% 的手术是经皮进行的。平均随访时间为(37±25)个月,无主动脉或手术相关死亡率。25名患者(31%)接受了再介入治疗,1年、3年和5年后不再接受再介入治疗的比例分别为84%、66%和55%。最常见的再干预是肢体移植支架植入术(23%)和II型内漏栓塞术(14%)。肢体闭塞率为 9%,有三名患者(4%)的远端内植物移位超过 5 毫米。29%的患者出现持续的II型内漏,41%的患者动脉瘤直径稳定,38%的患者直径缩小。随访期间出现了 3 个 III 型内漏(4%),需要进行 4 次开放式转换(5%)。没有任何已知的风险因素(包括在 IFU 以外进行的治疗)可预测再次介入治疗:结论:使用 INCRAFT 支架移植系统治疗肾下主动脉瘤是安全和成功的。结论:使用 INCRAFT 支架移植物系统治疗肾下主动脉瘤是安全和成功的,但在随访过程中,为了保持内移植物的通畅并防止动脉瘤生长,有必要进行大量的再介入治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.00
自引率
13.30%
发文量
603
审稿时长
50 days
期刊介绍: Annals of Vascular Surgery, published eight times a year, invites original manuscripts reporting clinical and experimental work in vascular surgery for peer review. Articles may be submitted for the following sections of the journal: Clinical Research (reports of clinical series, new drug or medical device trials) Basic Science Research (new investigations, experimental work) Case Reports (reports on a limited series of patients) General Reviews (scholarly review of the existing literature on a relevant topic) Developments in Endovascular and Endoscopic Surgery Selected Techniques (technical maneuvers) Historical Notes (interesting vignettes from the early days of vascular surgery) Editorials/Correspondence
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