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Andreu M. Climent

Publications and source records attributed to Andreu M. Climent.

2 recordsLinked to original sources

Synthetic Electrogram Generation with Variational Autoencoders for ECGI

Atrial fibrillation (AF) is the most prevalent sustained cardiac arrhythmia, and its clinical assessment requires accurate characterization of atrial electrical activity. Noninvasive electrocardiographic imaging (ECGI) combined with deep learning (DL) approaches for estimating intracardiac electrograms (EGMs) from body surface potentials (BSPMs) has shown promise, but progress is hindered by the limited availability of paired BSPM-EGM datasets. To address this limitation, we investigate variational autoencoders (VAEs) for the generation of synthetic multichannel atrial EGMs. Two models are proposed: a sinus rhythm-specific VAE (VAE-S) and a class-conditioned VAE (VAE-C) trained on both sinus rhythm and AF signals. Generated EGMs are evaluated using morphological, spectral, and distributional similarity metrics. VAE-S achieves higher fidelity with respect to in silico EGMs, while VAE-C enables rhythm-specific generation at the expense of reduced sinus reconstruction quality. As a proof of concept, the generated EGMs are used for data augmentation in a downstream noninvasive EGM reconstruction task, where moderate augmentation improves estimation performance. These results demonstrate the potential of VAE-based generative modeling to alleviate data scarcity and enhance deep learning-based ECGI pipelines.

cs.LG

Volumetric Non-Invasive Cardiac Mapping for Accessible Global Arrhythmia Characterization

Cardiac arrhythmias are a major cause of morbidity and mortality increasing the risk of stroke, heart failure, and sudden cardiac death. Imageless electrocardiographic imaging (ECGI) provides a non invasive alternative to electrical mapping from body surface potentials, but conventional ECGI is confined to epicardial reconstructions and can miss arrhythmias originating in deeper myocardium. We address this by reconstructing three dimensional cardiac activity with a volumetric formulation that solves an inverse source problem via Green's functions, enabling full volume activation mapping and improved localization in anatomically complex regions. We evaluate the approach on simulated premature ventricular beats and on four challenging patient cases, a right ventricular outflow tract premature ventricular contraction, a left bundle branch block, a ventricular tachycardia, and Wolff Parkinson White, and additionally assess performance on an open source myocardial infarction dataset. Results show that volumetric ECGI recovers 3D activation and sharpens arrhythmia origin localization, achieving a 59.3% reduction in geodesic error between estimated and simulated origins relative to surface only methods; in patient cases, activation patterns align with clinical diagnoses. Overall, imageless volumetric ECGI offers accessible, non invasive 3D activation mapping that overcomes a core limitation of surface restricted techniques and may improve preprocedural planning, ablation target guidance, and selection or optimization of cardiac resynchronization therapy.

cs.CE