Abstract

Focal sources are potential targets for atrial fibrillation (AF) catheter ablation, but they can be time-consuming and challenging to identify when unipolar electrograms (EGM) are numerous and complex. Our aim was to apply deep learning (DL) to raw unipolar EGMs in order to automate putative focal sources detection. We included 78 patients from the Focal Source and Trigger (FaST) randomized controlled trial that evaluated the efficacy of adjunctive FaST ablation compared to pulmonary vein isolation alone in reducing AF recurrence. FaST sites were identified based on manual classification of sustained periodic unipolar QS EGMs over 5-s. All periodic unipolar EGMs were divided into training (n = 10,004) and testing cohorts (n = 3,180). DL was developed using residual convolutional neural network to discriminate between FaST and non-FaST. A gradient-based method was applied to interpret the DL model. DL classified FaST with a receiver operator characteristic area under curve of 0.904 ± 0.010 (cross-validation) and 0.923 ± 0.003 (testing). At a prespecified sensitivity of 90%, the specificity and accuracy were 81.9 and 82.5%, respectively, in detecting FaST. DL had similar performance (sensitivity 78%, specificity 89%) to that of FaST re-classification by cardiologists (sensitivity 78%, specificity 79%). The gradient-based interpretation demonstrated accurate tracking of unipolar QS complexes by select DL convolutional layers. In conclusion, our novel DL model trained on raw unipolar EGMs allowed automated and accurate classification of FaST sites. Performance was similar to FaST re-classification by cardiologists. Future application of DL to classify FaST may improve the efficiency of real-time focal source detection for targeted AF ablation therapy.

Highlights

  • The pathogenesis of atrial fibrillation (AF) is complex, potentially involving localized drivers and abnormal atrial substrate outside the pulmonary veins (Heijman et al, 2016), which may account for the poor long-term success of pulmonary vein isolation (PVI) alone (Ganesan et al, 2013)

  • We have developed a pragmatic focal source detection algorithm, known as Focal Source and Trigger (FaST) mapping, where bipolar and unipolar EGMs are analyzed for periodicity and unipolar QS features as footprints of centrifugal wave propagation (Gizurarson et al, 2016; Kochhauser et al, 2017)

  • In a randomized controlled trial, FaST sites were widely distributed in PV and extra-PV regions in all patients, and their ablation reduced AF recurrence compared to PVI alone (Chauhan et al, 2020; Nayyar et al, 2020)

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Summary

Introduction

The pathogenesis of atrial fibrillation (AF) is complex, potentially involving localized drivers and abnormal atrial substrate outside the pulmonary veins (Heijman et al, 2016), which may account for the poor long-term success of pulmonary vein isolation (PVI) alone (Ganesan et al, 2013). Automated Focal Source Detection in AF in humans is challenging owing to the low spatial resolution of mapping techniques (Roney et al, 2017) and complex electrogram (EGM) features (DeBakker and Wittkampf, 2010). To address these challenges, we have developed a pragmatic focal source detection algorithm, known as Focal Source and Trigger (FaST) mapping, where bipolar and unipolar EGMs are analyzed for periodicity and unipolar QS features as footprints of centrifugal wave propagation (Gizurarson et al, 2016; Kochhauser et al, 2017). This can be challenging when unipolar EGMs appear fractionated and non-stationary over 5-s recordings

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