Computational quantitative flow ratio to assess functional severity of coronary artery stenosis.

狭窄 冠状动脉血流储备 动脉 血流 接收机工作特性 流量(数学)
作者
Daan Ties,Randy van Dijk,Gabija Pundziute,Erik Lipsic,Ton E. Vonck,Ad F. M. van den Heuvel,Rozemarijn Vliegenthart,Matthijs Oudkerk,Pim van der Harst
出处
期刊:International Journal of Cardiology [Elsevier]
卷期号:271: 36-41 被引量:11
标识
DOI:10.1016/j.ijcard.2018.05.002
摘要

Abstract Background Computational quantitative flow ratio (QFR) based on 3-dimensional quantitative coronary angiography (3D QCA) analysis offers the opportunity to assess the significance of coronary artery disease (CAD) without using an invasive pressure wire or inducing hyperemia. This study aimed to evaluate the diagnostic performance of QFR compared to wire-based fractional flow reserve (FFR) and to validate the previously reported QFR cut-off value of >0.90 to safely rule out functionally significant CAD. Methods QFR was retrospectively derived from standard-care coronary angiograms. Correlation and agreement of fixed-flow QFR (fQFR) and contrast-flow QFR (cQFR) models with invasive wire-based FFR was calculated. Diagnostic performance of QFR was evaluated at different QFR cut-off values defining significant CAD (FFR ≤ 0.80). Results 101 vessels in 96 patients who underwent FFR were studied. Mean FFR was 0.87 ± 0.08 and 21 of 101 (21%) vessels had an FFR ≤ 0.80. Correlation of fQFR and cQFR with FFR was r = 0.71 (p  0.80 defining non-significant CAD, respectively. fQFR > 0.90 was present in 34 (34%) and cQFR > 0.90 in 39 (39%) vessels. For both QFR models, none of the vessels with QFR > 0.90 had an FFR ≤ 0.80. Conclusions QFR appears to be a safe and effective gatekeeper to wire-based FFR when applying a QFR threshold of >0.90 to rule out significant CAD. Further prospective research is required to establish QFR in the real-life setting of functional CAD assessment in the catheterization laboratory.

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
冷冷完成签到,获得积分10
1秒前
okayu完成签到,获得积分10
1秒前
1秒前
yue完成签到 ,获得积分10
1秒前
2秒前
缓慢的涵瑶完成签到,获得积分10
2秒前
yangyangzijiajia完成签到,获得积分10
3秒前
陈欣茹发布了新的文献求助10
4秒前
思思发布了新的文献求助10
4秒前
杨家乐完成签到,获得积分10
4秒前
su完成签到,获得积分10
4秒前
5秒前
Tomgoodjob发布了新的文献求助10
5秒前
船舵发布了新的文献求助10
5秒前
Aoibision发布了新的文献求助10
6秒前
6秒前
叼着奶瓶上天完成签到,获得积分10
6秒前
csy发布了新的文献求助10
6秒前
6秒前
7秒前
8秒前
霍则风发布了新的文献求助20
8秒前
bkagyin应助张哈哈采纳,获得10
8秒前
llldosg发布了新的文献求助10
9秒前
9秒前
烈酒一醉方休完成签到 ,获得积分10
9秒前
Zhengzhang完成签到 ,获得积分10
9秒前
思源应助南南采纳,获得10
10秒前
Sunnig盈完成签到,获得积分10
10秒前
carly发布了新的文献求助10
11秒前
船舵完成签到,获得积分10
11秒前
DUN完成签到,获得积分10
11秒前
丘比特应助如意的向彤采纳,获得10
11秒前
lindo完成签到 ,获得积分10
11秒前
11秒前
卷心菜完成签到,获得积分10
12秒前
w9412发布了新的文献求助10
12秒前
12秒前
TY应助英勇代荷采纳,获得10
13秒前
ding应助佳佳爱学习采纳,获得10
13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
Handbook of pharmaceutical excipients, Ninth edition 5000
Aerospace Standards Index - 2026 ASIN2026 2000
Digital Twins of Advanced Materials Processing 2000
Social Cognition: Understanding People and Events 1200
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6036618
求助须知:如何正确求助?哪些是违规求助? 7755510
关于积分的说明 16215236
捐赠科研通 5182648
什么是DOI,文献DOI怎么找? 2773624
邀请新用户注册赠送积分活动 1756892
关于科研通互助平台的介绍 1641263