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首页> 外文期刊>Computers in Biology and Medicine >Regional conduction velocity calculation from clinical multichannel electrograms in human atria
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Regional conduction velocity calculation from clinical multichannel electrograms in human atria

机译:人类阿里亚临床多通道电子图的区域传导速度计算

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Abstract Background During atrial fibrillation, heterogeneities and anisotropies result in a chaotic propagation of the depolarization wavefront. The electrophysiological parameter called conduction velocity (CV) influences the propagation pattern over the atrium. We present a method that determines the regional CV for deformed catheter shapes, which result due to the catheter movement and changing wall contact. Methods The algorithm selects stable catheter positions, finds the local activation times (LAT), considers the wall contact and calculates all CV estimates within the area covered by the catheter. The method is evaluated with simulated data and then applied to four clinical data sets. Both sinus rhythm activity as well as depolarization wavefronts initiated by stimulation are analyzed. The regional CV is compared with the fractionation duration (FD) and peak-to-peak (P2P) voltages. A speed of 0.5?m/s was defined to create the simulated LAT. Results After analyzing the simulated LAT with clinical catheter spatial coordinates, the median CV of 0.5?m/s with an interquartile range of 0.22 and exact CV direction vectors were obtained. For clinical cases, the CV magnitude range of 0.08?m/s to 1.0?m/s was obtained. The P2P amplitude of 0.7?mV to 3.7?mV and the mean FD from 40.79ms to 48.66ms was obtained. The correlation of 0.86 was observed between CV and P2P amplitude, and 0.62 between CV and FD. Conclusion In this paper, a method is presented and validated which calculates the CV for the deformed catheter and changing wall contact. In an exemplary clinical data set correlation between regional CV with FD and the P2P voltage was observed. Highlights ? Regional CV calculated for stable catheter positions and individual cardiac excitation. ? The algorithm works for different catheter shapes and changing wall contact. ? The algorithm has been benchmarked with simulated data. ? A novel method to identify critical, slow conducting substrate.
机译:在心房颤动,异质性和各向同性期间的抽象背景导致去极化波前的混沌传播。称为传导速度(CV)的电生理学参数影响荨麻疹的传播模式。我们提出了一种方法,该方法确定变形导管形状的区域CV,这导致导致导管运动和壁接触改变。方法该算法选择稳定的导管位置,找到局部激活时间(LAT),认为壁接触并计算导管覆盖的面积内的所有CV估计。使用模拟数据评估该方法,然后应用于四个临床数据集。分析窦性心律活动以及通过刺激引发的去极化波线。将区域CV与分馏持续时间(FD)和峰 - 峰(P2P)电压进行比较。定义了0.5μm/ s的速度以创建模拟LAT。结果在用临床导管空间坐标分析模拟LAT后,获得了0.5μm/ s的中值CV,其间隔位为0.22和精确的CV方向矢量。对于临床病例,获得了0.08Ωm/ s至1.0μm/ s的CV幅度范围。将P2P幅度为0.7Ω·mV至3.7·mV,并获得40.79ms至48.66ms的平均FD。在CV和P2P幅度之间观察到0.86的相关性,CV和FD之间的0.62。结论在本文中,提出和验证了一种方法,其计算变形导管的CV和改变壁接触。在示例性临床资料中,观察到具有FD和P2P电压的区域CV之间的相关性。强调 ?为稳定的导管位置和单独的心脏激发计算区域简历。还该算法适用于不同的导管形状和改变壁触点。还该算法已通过模拟数据进行基准测试。还一种识别临界,慢导电底物的新方法。

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