利用光子计数1000 fps高速血管造影(HSA)进行二维速度分布估计的几何独立对比度稀释梯度(CDG)速度测定。

Kyle A Williams, Allison Shields, S V Setlur Nagesh, Daniel R Bednarek, Stephen Rudin, Ciprian N Ionita
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引用次数: 0

摘要

目的:先前的研究已经证明了对比稀释梯度(CDG)分析在确定1000 fps高速血管造影(HSA)大血管流速分布方面的有效性。然而,该方法需要提取血管中心线,这使得它只适用于使用高度特异性造影剂注射技术的非弯曲几何形状。本研究旨在消除对流动方向先验知识的需求,并修改容器采样方法,使算法对非线性几何形状更具鲁棒性。材料和方法:使用XC-Actaeon (Varex Inc.)光子计数检测器,通过台式流环在体外获得1000 fps的HSA,并在计算机上使用计算流体动力学(CFD)模拟中的被动标量输运模型。CDG分析是通过在整个船舶上进行网格线采样获得的,随后在x和y方向上进行1D速度测量。通过共同配准得到的速度图,将CDG分量速度矢量得到的速度大小与CFD结果对齐,并在对1毫秒速度分布进行时间平均后,使用每种方法像素值之间的平均绝对百分比误差(MAPE)进行比较。结果:与CFD(颈动脉分叉入口MAPE为18%,颈内动脉瘤MAPE为27%)相比,在整个采集过程中对比度充分饱和的区域显示出一致性,完成时间分别为137秒和5.8秒。结论:如果造影剂注入足以提供梯度,造影剂在系统中的扩散可以忽略不计,CDG可用于获得血管病变内和周围的速度分布。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Geometrically independent contrast dilution gradient (CDG) velocimetry using photon-counting 1000 fps High Speed Angiography (HSA) for 2D velocity distribution estimation.

Purpose: Previous studies have demonstrated the efficacy of contrast dilution gradient (CDG) analysis in determining large vessel velocity distributions from 1000 fps high-speed angiography (HSA). However, the method required vessel centerline extraction, which made it applicable only to non-tortuous geometries using a highly specific contrast injection technique. This study seeks to remove the need for a priori knowledge regarding the direction of flow and modify the vessel sampling method to make the algorithm more robust to non-linear geometries.

Materials and methods: 1000 fps HSA acquisitions were obtained in vitro with a benchtop flow loop using the XC-Actaeon (Varex Inc.) photon-counting detector, and in silico using a passive-scalar transport model within a computational fluid dynamics (CFD) simulation. CDG analyses were obtained using gridline sampling across the vessel, and subsequent 1D velocity measurement in both the x- and y-directions. The velocity magnitudes derived from the component CDG velocity vectors were aligned with CFD results via co-registration of the resulting velocity maps and compared using mean absolute percent error (MAPE) between pixels values in each method after temporal averaging of the 1-ms velocity distributions.

Results: Regions well-saturated with contrast throughout the acquisition showed agreement when compared to CFD (MAPE of 18% for the carotid bifurcation inlet and MAPE of 27% for the internal carotid aneurysm), with respective completion times of 137 seconds and 5.8 seconds.

Conclusions: CDG may be used to obtain velocity distributions in and surrounding vascular pathologies provided the contrast injection is sufficient to provide a gradient, and diffusion of contrast through the system is negligible.

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