腔内波前重建和三维传导速度估算的验证。

Computing in cardiology Pub Date : 2019-01-01 Epub Date: 2020-02-24 DOI:10.22489/cinc.2019.420
Wilson W Good, Karli K Gillette, Jake A Bergquist, Brian Zenger, Jess Tate, Lindsay C Rupp, Devan Anderson, Gernot Plank, Rob S MacLeod
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引用次数: 0

摘要

简介:传导速度的变化是多种心脏异常的标志,但测量传导速度是一项挑战,尤其是在心肌容积内。在这项研究中,我们研究了一种新技术,它能从实验性心内膜记录中重建激活前沿并估算三维(3D)传导速度(CV):方法:我们从间歇采样的电图中重建激活轮廓,计算激活时间梯度的倒数和一系列流线,从而估算 CV:重建的激活时间与模拟值非常吻合,50% 至 70% 的节点绝对误差小于 1 毫秒。我们发现使用重建激活时间与模拟激活时间计算出的 CV 值非常接近。在所有重建的刺激部位,我们发现重建的 CV 与地面实况 CV 平均相差 3.8%:本研究使用模拟数据集来验证我们重建三维激活前沿和估计传导速度的方法。我们的研究结果表明,我们的方法可以从稀疏的测量结果中准确重建,从而使我们能够研究急性缺血、异位起搏或药物等实验干预所引起的激活变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Validation of Intramural Wavefront Reconstruction and Estimation of 3D Conduction Velocity.

Validation of Intramural Wavefront Reconstruction and Estimation of 3D Conduction Velocity.

Validation of Intramural Wavefront Reconstruction and Estimation of 3D Conduction Velocity.

Validation of Intramural Wavefront Reconstruction and Estimation of 3D Conduction Velocity.

Introduction: Changes in conduction velocity are indicative of a wide variety of cardiac abnormalities yet measuring conduction velocity is challenging, especially within the myocardial volume. In this study we investigated a novel technique to reconstruct activation fronts and estimate three-dimensional (3D) conduction velocity (CV) from experimental intramural recordings.

Methods: From the intermittently sampled electrograms we both reconstruct the activation profile and compute the reciprocal of the gradient of activation times and a series of streamlines that allows for the CV estimation.

Results: The reconstructed activation times agreed closely with simulated values, with 50% to 70% of the nodes ≤ 1ms of absolute error. We found close agreement between the CVs calculated using reconstructed versus simulated activation times. Across the reconstructed stimulation sites we saw that the reconstructed CV was on average 3.8% different than the ground truth CV.

Discussion: This study used simulated datasets to validate our methods for reconstructing 3D activation fronts and estimating conduction velocities. Our results indicate that our method allows accurate reconstructions from sparse measurements, thus allowing us to examine changes in activation induced by experimental interventions such as acute ischemia, ectopic pacing, or drugs.

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