Abstract

Background

Complexity and signal recurrence metrics obtained from body surface potential mapping (BSPM) allow quantifying atrial fibrillation (AF) substrate complexity. This study aims to correlate electrocardiographic imaging (ECGI) detected reentrant patterns with BSPM-calculated signal complexity and recurrence metrics.

Methods

BSPM signals were recorded from 28 AF patients (17 male, 11 women, 62.69 ± 8.09 y.o.), followed by ECGI calculation. Signal complexity and recurrence metrics were computed on BSPM and ECGI signals. Rotors per second and rotor duration were computed on ECGI signals for each atrium and the whole atrial surface. Correlation between BSPM metrics and ECGI reentrant patterns for the entire atrial surface and for left atrium (LA) and right atrium (RA) were analyzed.

Results

Atrial complexity and recurrence metrics strongly correlated when computed on BSPM and ECGI. Higher sample entropy and relative harmonic energy (RHE) correlated with rotors of short duration. The highest dominant frequency of the ECGI signals did not correlate with the reentrant activity of the ECGI. Higher short- and long-term recurrence of BSPM signals correlated with longer duration rotors, particularly for long-term recurrence (rLA=0.74 vs. rRA=0.42). Only ECGI-based reentrant parameters showed higher LA complexity compared to RA (p < 0.05).

Conclusions

BSPM metrics strongly correlate with metrics measured on ECGI signals. BSPM metrics indicate a more elevated atrial electro-structural remodeling aligned with more short-duration rotors from ECGI computations. Although BSPM delivers qualitative AF reentry data, ECGI remains essential for identifying regional substrate complexity.

Details

Title
Complexity and recurrence of body surface electrocardiograms correlate with estimated reentrant atrial activity using electrocardiographic imaging in atrial fibrillation patients
Author
Molero, Rubén; Meste, Olivier; Peeters, Ralf; Karel, Joël; Bonizzi, Pietro; Guillem, María S
Pages
1-13
Section
Research
Publication year
2025
Publication date
2025
Publisher
BioMed Central
e-ISSN
14712261
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3165418180
Copyright
© 2025. This work is licensed under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.