Impact of Baseline and Postprocedural Intravascular Ultrasound Findings on 1-Year Primary Patency After Drug-Coated Balloon Treatment of Femoropopliteal Lesions

医学 再狭窄 血管内超声 管腔(解剖学) 气球 放射科 钙化 接收机工作特性 危险系数 闭塞 支架 外科 内科学 置信区间
作者
Kazunori Horie,Akiko Tanaka,Masataka Taguri,Naoto Inoue
出处
期刊:Journal of Endovascular Therapy [SAGE]
卷期号:29 (1): 66-75 被引量:31
标识
DOI:10.1177/15266028211058683
摘要

Drug-coated balloons (DCBs) are commonly used for endovascular treatment of femoropopliteal lesions. Here, we employed intravascular ultrasound (IVUS) to investigate the predictors of restenosis after DCB treatment.This retrospective and single-center study was performed to examine 1-year primary patency after DCB treatment and to identify the risk factors for restenosis by analyzing clinical characteristics, angiographic findings, and IVUS measurements. We included 111 consecutive patients undergoing DCB treatment for de novo femoropopliteal lesions at our hospital from July 2018 to March 2020.The primary patency rate was found to be 80.0% at 1 year. The Cox proportional hazard multivariate analysis revealed that restenosis was independently associated with chronic total occlusion (CTO; p < 0.001), circumferential calcification (p = 0.023), and smaller postprocedural minimum lumen area (MLA; p = 0.036). Furthermore, receiver operating characteristic curve analysis showed that the cutoff value of postprocedural MLA to prevent restenosis was 12.7 mm2, with an area under the curve of 0.774 (p< 0.001). The multivariate analysis indicated that patients with a postprocedural MLA below 12.7 mm2 (n = 44) had a significantly smaller distal reference vessel size (p < 0.001) compared to those with a postprocedural MLA over 12.7 mm2 (n = 67).Restenosis after DCB treatment was shown to correlate with CTO, circumferential calcification, and postprocedural MLA as evaluated by IVUS. Moreover, smaller vessel sizes might represent a particular challenge to the DCB strategy due to the difficulty of restoring a sufficient postprocedural lumen area by balloon dilatation.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
科研通AI6.1应助yx采纳,获得10
刚刚
领导范儿应助noodles采纳,获得10
刚刚
xxdn完成签到,获得积分10
刚刚
吕布发布了新的文献求助10
1秒前
olivia完成签到,获得积分10
2秒前
最佳损友完成签到,获得积分0
2秒前
充电宝应助马上毕业采纳,获得10
2秒前
搞怪哑铃发布了新的文献求助10
3秒前
3秒前
3秒前
小马甲应助真实的咖啡采纳,获得30
4秒前
1z2x3s发布了新的文献求助10
4秒前
suesue发布了新的文献求助10
4秒前
科研通AI6.2应助zbzfp采纳,获得10
4秒前
猪猪hero发布了新的文献求助10
4秒前
sghsh完成签到,获得积分10
5秒前
潇洒的妙芙完成签到,获得积分10
5秒前
慕青应助科技梦采纳,获得10
5秒前
MSYzack发布了新的文献求助10
5秒前
Iva完成签到 ,获得积分10
6秒前
LKT发布了新的文献求助10
6秒前
林林林林完成签到,获得积分10
7秒前
z!完成签到 ,获得积分10
8秒前
9秒前
英俊的铭应助One采纳,获得10
12秒前
13秒前
卡拉米完成签到,获得积分10
13秒前
Owen应助慕子默采纳,获得10
14秒前
cly发布了新的文献求助10
15秒前
15秒前
传奇3应助天马行空采纳,获得10
16秒前
风q完成签到,获得积分10
16秒前
科研通AI6.2应助身处人海采纳,获得10
17秒前
科研通AI6.1应助卡拉米采纳,获得10
17秒前
17秒前
18秒前
青人完成签到,获得积分10
18秒前
慕青应助wpie99采纳,获得10
18秒前
jessie发布了新的文献求助10
18秒前
万能图书馆应助雨山采纳,获得30
18秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Kinesiophobia : a new view of chronic pain behavior 2000
Research for Social Workers 1000
Psychology and Work Today 800
Mastering New Drug Applications: A Step-by-Step Guide (Mastering the FDA Approval Process Book 1) 800
Kinesiophobia : a new view of chronic pain behavior 600
Signals, Systems, and Signal Processing 510
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5896423
求助须知:如何正确求助?哪些是违规求助? 6710455
关于积分的说明 15734091
捐赠科研通 5018926
什么是DOI,文献DOI怎么找? 2702749
邀请新用户注册赠送积分活动 1649540
关于科研通互助平台的介绍 1598639