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Repolarization abnormalities unmasked with a 252‐lead BSM system in patients with ARVC and healthy gene carriers

Background: Diagnosing arrhythmogenic right ventricular cardiomyopathy (ARVC) at an early stage can be challenging even after ECG recording and a combination of several imaging techniques. The purpose of this study was to explore if a body surface mapping (BSM) system with 252‐leads could identify r...

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Autores principales: Kommata, Varvara, Sciaraffia, Elena, Blomström‐Lundqvist, Carina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9314798/
https://www.ncbi.nlm.nih.gov/pubmed/35077593
http://dx.doi.org/10.1111/pace.14456
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author Kommata, Varvara
Sciaraffia, Elena
Blomström‐Lundqvist, Carina
author_facet Kommata, Varvara
Sciaraffia, Elena
Blomström‐Lundqvist, Carina
author_sort Kommata, Varvara
collection PubMed
description Background: Diagnosing arrhythmogenic right ventricular cardiomyopathy (ARVC) at an early stage can be challenging even after ECG recording and a combination of several imaging techniques. The purpose of this study was to explore if a body surface mapping (BSM) system with 252‐leads could identify repolarization abnormalities and thereby diagnose early stages of ARVC. Methods: ARVC patients, gene carriers without signs of ARVC and controls underwent a 12‐lead resting ECG, signal‐averaged ECG, echocardiography, 24‐hours Holter monitoring, and BSM with electrocardiographic imaging (ECGI). All 252‐leads, divided into four quadrants of the vest, were analyzed regarding concordances between T wave polarity and QRS main vector. Results: Of 40 patients included there were 12 ARVC patients, 20 gene carriers, and 8 controls. The ARVC patients had two different repolarization patterns, one with more pronounced negative T waves at the lower left panel and another with mixed changes that clearly differed from the controls, all of whom had a normal 12 lead ECGs and consistent repolarization patterns on their BSM recordings. The patterns observed in ARVC patients were also present in 5/20 (25%) gene carriers, three of whom had normal resting ECG. A novel repolarization index successfully detected all ARVC patients and 88% of gene carriers with pathologic repolarization pattern. Conclusions: The finding that abnormal repolarization patterns could be unmasked by BSM in 25% of healthy gene carriers, suggests that it may potentially be a useful tool for identifying early manifestations of ARVC. Further and larger studies are warranted to assess its diagnostic accuracy.
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spelling pubmed-93147982022-07-30 Repolarization abnormalities unmasked with a 252‐lead BSM system in patients with ARVC and healthy gene carriers Kommata, Varvara Sciaraffia, Elena Blomström‐Lundqvist, Carina Pacing Clin Electrophysiol Electrophysiology Background: Diagnosing arrhythmogenic right ventricular cardiomyopathy (ARVC) at an early stage can be challenging even after ECG recording and a combination of several imaging techniques. The purpose of this study was to explore if a body surface mapping (BSM) system with 252‐leads could identify repolarization abnormalities and thereby diagnose early stages of ARVC. Methods: ARVC patients, gene carriers without signs of ARVC and controls underwent a 12‐lead resting ECG, signal‐averaged ECG, echocardiography, 24‐hours Holter monitoring, and BSM with electrocardiographic imaging (ECGI). All 252‐leads, divided into four quadrants of the vest, were analyzed regarding concordances between T wave polarity and QRS main vector. Results: Of 40 patients included there were 12 ARVC patients, 20 gene carriers, and 8 controls. The ARVC patients had two different repolarization patterns, one with more pronounced negative T waves at the lower left panel and another with mixed changes that clearly differed from the controls, all of whom had a normal 12 lead ECGs and consistent repolarization patterns on their BSM recordings. The patterns observed in ARVC patients were also present in 5/20 (25%) gene carriers, three of whom had normal resting ECG. A novel repolarization index successfully detected all ARVC patients and 88% of gene carriers with pathologic repolarization pattern. Conclusions: The finding that abnormal repolarization patterns could be unmasked by BSM in 25% of healthy gene carriers, suggests that it may potentially be a useful tool for identifying early manifestations of ARVC. Further and larger studies are warranted to assess its diagnostic accuracy. John Wiley and Sons Inc. 2022-03-13 2022-04 /pmc/articles/PMC9314798/ /pubmed/35077593 http://dx.doi.org/10.1111/pace.14456 Text en © 2022 The Authors. Pacing and Clinical Electrophysiology published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Electrophysiology
Kommata, Varvara
Sciaraffia, Elena
Blomström‐Lundqvist, Carina
Repolarization abnormalities unmasked with a 252‐lead BSM system in patients with ARVC and healthy gene carriers
title Repolarization abnormalities unmasked with a 252‐lead BSM system in patients with ARVC and healthy gene carriers
title_full Repolarization abnormalities unmasked with a 252‐lead BSM system in patients with ARVC and healthy gene carriers
title_fullStr Repolarization abnormalities unmasked with a 252‐lead BSM system in patients with ARVC and healthy gene carriers
title_full_unstemmed Repolarization abnormalities unmasked with a 252‐lead BSM system in patients with ARVC and healthy gene carriers
title_short Repolarization abnormalities unmasked with a 252‐lead BSM system in patients with ARVC and healthy gene carriers
title_sort repolarization abnormalities unmasked with a 252‐lead bsm system in patients with arvc and healthy gene carriers
topic Electrophysiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9314798/
https://www.ncbi.nlm.nih.gov/pubmed/35077593
http://dx.doi.org/10.1111/pace.14456
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