Volumetric soft tissue perfusion assessment on a region basis from x-ray angiography images: Motion compensation.

Medical physics Pub Date : 2025-05-13 DOI:10.1002/mp.17870
Katsuyuki Taguchi, Shalini Subramanian, Andreia V Faria, W Paul Segars
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Abstract

Background: Assessing the soft tissue perfusion quantitatively in interventional suites before, during, and after interventional procedures is desired. The method, if possible, has to assess the perfusion volumetrically and quantitatively, be robust against lesion overlaps and patient motion, require no additional radiation dose, be quick (possibly in real-time), and fit to the clinical workflow well. We have developed a method called IPEN (for Intra-operative PErfusion assessment with No gantry rotation) that has potential to accomplish all of the desired goals except for the patient motion. The innovation with IPEN is not to reconstruct volumetric images, but to estimate enhancement of multiple three-dimensional regions-of-interest directly from x-ray projections acquired at one angle.

Purpose: To further develop the IPEN method such that it can compensate for patient motion when the patient moves quickly during the angiography scan but stays still otherwise.

Methods: The proposed motion-compensating IPEN (MCI) consists of the following three steps: (Step 1) The time segment is broken into multiple segments, that is, a set of rapid motion segments and a set of stationary segments; (Step 2) the MCI estimates ROI enhancement within each stationary segment; and (Step 3) MCI connects segments. The performance of the proposed MCI and the original IPEN were assessed using the digital perfusion phantom, simulating 13 ischemic stroke "patients." The head moved within 0.6 s each time, and seven times during 16-s scans; motion magnitude parameter a (for ± a mm and ± a degrees) was 0.0 (no motion), 0.5, 2.0, 5.0, and 25.0 for each scan. The accuracy of time-enhancement curves (TECs) and calculated perfusion-like parameter ("max-slope" for the maximum of slope of TEC; similar to Patlak plot analysis) was assessed. In addition, the effect of the motion segments on the accuracy of the estimated TEC has been studied systematically.

Results: Head motion induced very severe inconsistency and artifact in synthesized digital subtraction angiography images. The original IPEN had disjoint TECs, and the correlation coefficients (r) against the true values decreased from 0.475 at a = 0.5 to 0.023 at a = 25.0. The proposed MCI provided smooth and accurate TECs with r = 0.995 at a = 0.5 and r = 0.989 at a = 25.0. The 𝓁2-norm of the error vectors of the max-slope values was 5.6-64.2 (d.l.) for the original IPEN, whereas it was < 0.1 for the MCI for the motion magnitudes investigated. There was an strong linear relationship between the non-linearity of the derivative of TECs and biases in TEC: r was 0.999. MCI would have a significant bias when a lengthy motion occurs when an ROI enhancement changes non-linearly during the time.

Conclusion: The proposed MCI can compensate for the patient motion very effectively and accurately when the motion is not continuous and the ROI enhancement does not change non-linearly and significantly during the motion segment.

基于x线血管造影图像的区域容量软组织灌注评估:运动补偿。
背景:需要在介入前、介入中、介入后对软组织灌注进行定量评估。如果可能的话,该方法必须对灌注进行体积和定量评估,对病变重叠和患者运动具有鲁棒性,不需要额外的辐射剂量,快速(可能是实时的),并且很好地适应临床工作流程。我们已经开发了一种称为IPEN(术中灌注评估,无龙门旋转)的方法,它有可能实现除患者运动外的所有预期目标。IPEN的创新之处不是重建体积图像,而是直接从一个角度获得的x射线投影估计多个三维感兴趣区域的增强。目的:进一步发展IPEN方法,使其能够补偿患者在血管造影扫描期间快速移动而在其他情况下保持静止时的运动。方法:本文提出的运动补偿IPEN (MCI)包括以下三个步骤:(1)将时间片段分解为多个片段,即一组快速运动片段和一组静止运动片段;(步骤2)MCI估计每个平稳段内的ROI增强;(步骤3)MCI连接段。通过模拟13例缺血性脑卒中患者,对所提出的MCI和原始IPEN的性能进行了评估。头部每次在0.6 s内移动,在16-s扫描期间移动了7次;每次扫描的运动幅度参数a(±1毫米和±1度)分别为0.0(无运动)、0.5、2.0、5.0和25.0。时间增强曲线(TEC)和计算的类灌注参数(TEC斜率最大值为“max-slope”)的准确性;与Patlak plot分析相似)。此外,还系统地研究了运动段对估计TEC精度的影响。结果:头部运动导致合成数字减影血管造影图像出现严重的不一致和伪影。原始IPEN的tec不相交,与真值的相关系数(r)从a = 0.5时的0.475下降到a = 25.0时的0.023。所提出的MCI提供了平滑准确的tec,在a = 0.5时r = 0.995,在a = 25.0时r = 0.989。原始IPEN的最大斜率误差向量𝓁2-norm为5.6-64.2 (d.l.),结论:在运动不连续且ROI增强在运动段内不发生非线性显著变化的情况下,所提出的MCI可以非常有效、准确地补偿患者的运动。
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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