Abstract

BackgroundAtrial electrograms recorded from the epicardium provide an important tool for studying the initiation, perpetuation, and treatment of AF. However, the properties of these electrograms depend largely on the properties of the electrode arrays that are used for recording these signals. MethodIn this study, we use the electrode's transfer function to model and analyze the effect of electrode size on the properties of measured electrograms. To do so, we use both simulated as well as clinical data. To simulate electrogram arrays we use a two-dimensional (2D) electrogram model as well as an action propagation model. For clinical data, however, we first estimate the trans-membrane current for a higher resolution 2D modeled cell grid and later use these values to interpolate and model electrograms with different electrode sizes. ResultsWe simulate electrogram arrays for 2D tissues with 3 different levels of heterogeneity in the conduction and stimulation pattern to model the inhomogeneous wave propagation observed during atrial fibrillation. Four measures are used to characterize the properties of the simulated electrogram arrays of different electrode sizes. The results show that increasing the electrode size increases the error in LAT estimation and decreases the length of conduction block lines. Moreover, visual inspection also shows that the activation maps generated by larger electrodes are more homogeneous with a lower number of observed wavelets. The increase in electrode size also increases the low voltage areas in the tissue while decreasing the slopes and the number of detected deflections. The effect is more pronounced for a tissue with a higher level of heterogeneity in the conduction pattern. Similar conclusions hold for the measurements performed on clinical data. ConclusionThe electrode size affects the properties of recorded electrogram arrays which can respectively complicate our understanding of atrial fibrillation. This needs to be considered while performing any analysis on the electrograms or comparing the results of different electrogram arrays.

Highlights

  • Recording and processing of electrograms (EGMs) is the cornerstone of mapping procedures guiding ablative therapies of cardiac arrhyth­ mias

  • We studied the effect of electrode size on the properties of the recorded electrograms

  • We started by simulated electrograms of 2D atrial tissues and present the effect of different electrode sizes on electrogram properties including the error in local activation time (LAT) estimation, the length of slow conduction or blocks (LSC/B) observed on the resulting activa­ tion map, percentage of observed low voltage areas (LVA), and the number of deflections in the recorded electrograms

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Summary

Introduction

Recording and processing of electrograms (EGMs) is the cornerstone of mapping procedures guiding ablative therapies of cardiac arrhyth­ mias. There are only a few studies investigating the effect of the electrode size on the properties of the unipolar electrograms using both electrophysi­ ological models and clinical recordings These properties include signal-to-noise ratio (SNR), fractionation level, voltage level, and the error in local activation time (LAT) estimation [8,9,10]. We exclusively investigate the effect of the electrode size on the properties of high resolution unipolar electrogram arrays by keeping the other parameters like inter-electrode distances and electrical wave propagation patterns fixed We use both clinical observation and elec­ trophysiological models that govern the wave propagation and elec­ trogram generation to analyze and investigate these effects.

Atrial tissue computer model
Electrode’s transfer function model
Modeling abnormal tissue
Clinical studies
Electrogram analysis
Effect of electrode size on electrogram properties
Effect of electrode size on the activation map
Optimal electrode diameter and inter-electrode distance
Maximum electrode size for recording scarred tissue
Clinical results
Changes in activation maps
Scaling electrograms’ amplitude
Discussion and conclusion
Study limitations
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