Abstract

BackgroundCardiac conduction properties exhibit large variability, and affect patient-specific arrhythmia mechanisms. However, it is challenging to clinically measure conduction velocity (CV), anisotropy and fibre direction. Our aim is to develop a technique to estimate conduction anisotropy and fibre direction from clinically available electrical recordings. MethodsWe developed and validated automated algorithms for estimating cardiac CV anisotropy, from any distribution of recording locations on the atrial surface. The first algorithm is for elliptical wavefront fitting to a single activation map (method 1), which works well close to the pacing location, but decreases in accuracy further from the pacing location (due to spatial heterogeneity in the conductivity and fibre fields). As such, we developed a second methodology for measuring local conduction anisotropy, using data from two or three activation maps (method 2: ellipse fitting to wavefront propagation velocity vectors from multiple activation maps). ResultsEllipse fitting to CV vectors from two activation maps (method 2) leads to an improved estimation of longitudinal and transverse CV compared to method 1, but fibre direction estimation is still relatively poor. Using three activation maps with method 2 provides accurate estimation, with approximately 70% of atrial fibres estimated within 20∘. We applied the technique to clinical activation maps to demonstrate the presence of heterogeneous conduction anisotropy, and then tested the effects of this conduction anisotropy on predicted arrhythmia dynamics using computational simulation. ConclusionsWe have developed novel algorithms for calculating CV and measuring the direction dependency of atrial activation to estimate atrial fibre direction, without the need for specialised pacing protocols, using clinically available electrical recordings.

Highlights

  • IntroductionAnatomy and structure affect atrial fibrillation (AF) mechanisms

  • Patient specific electrophysiology, anatomy and structure affect atrial fibrillation (AF) mechanisms

  • We applied the technique to clinical activation maps to demonstrate the presence of heterogeneous conduction anisotropy, and tested the effects of this conduction anisotropy on predicted arrhythmia dynamics using computational simulation

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Summary

Introduction

Anatomy and structure affect atrial fibrillation (AF) mechanisms. These features exhibit large variability between patients, and change with AF progression. Changes that occur during AF that modify atrial conduction include down-regulation and lateralisation of connexins, deposition of collagen and interstitial fibrosis, as well as changes in atrial fibre direction, including fibre disarray [1, 2]. Each of these factors affect the heterogeneity and anisotropy of atrial conduction. Results: Ellipse fitting to CV vectors from two activation maps (method 2) leads to an improved estimation of longitudinal and transverse CV compared to method 1, but fibre direction estimation is still relatively poor

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