Cargando…
Characterizing the clinical implementation of a novel activation-repolarization metric to identify targets for catheter ablation of ventricular tachycardias using computational models
Identification of targets for catheter ablation of ventricular tachycardias (VTs) remains a significant challenge. VTs are often driven by re-entrant circuits resulting from a complex interaction between the front (activation) and tail (repolarization) of the electrical wavefront. Most mapping techn...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538827/ https://www.ncbi.nlm.nih.gov/pubmed/31009930 http://dx.doi.org/10.1016/j.compbiomed.2019.03.018 |
_version_ | 1783422249137602560 |
---|---|
author | Campos, Fernando O. Orini, Michele Taggart, Peter Hanson, Ben Lambiase, Pier D. Porter, Bradley Rinaldi, Christopher Aldo Gill, Jaswinder Bishop, Martin J. |
author_facet | Campos, Fernando O. Orini, Michele Taggart, Peter Hanson, Ben Lambiase, Pier D. Porter, Bradley Rinaldi, Christopher Aldo Gill, Jaswinder Bishop, Martin J. |
author_sort | Campos, Fernando O. |
collection | PubMed |
description | Identification of targets for catheter ablation of ventricular tachycardias (VTs) remains a significant challenge. VTs are often driven by re-entrant circuits resulting from a complex interaction between the front (activation) and tail (repolarization) of the electrical wavefront. Most mapping techniques do not take into account the tissue repolarization which may hinder the detection of ablation targets. The re-entry vulnerability index (RVI), a recently proposed mapping procedure, incorporates both activation and repolarization times to uncover VT circuits. The method showed potential in a series of experiments, but it still requires further development to enable its incorporation into a clinical protocol. Here, in-silico experiments were conducted to thoroughly assess RVI maps constructed under clinically-relevant mapping conditions. Within idealized as well as anatomically realistic infarct models, we show that parameters of the algorithm such as the search radius can significantly alter the specificity and sensitivity of the RVI maps. When constructed on sparse grids obtained following various placements of clinical recording catheters, RVI maps can identify vulnerable regions as long as two electrodes were placed on both sides of the line of block. Moreover, maps computed during pacing without inducing VT can reveal areas of abnormal repolarization and slow conduction but not directly vulnerability. In conclusion, the RVI algorithm can detect re-entrant circuits during VT from low resolution mapping grids resembling the clinical setting. Furthermore, RVI maps may provide information about the underlying tissue electrophysiology to guide catheter ablation without the need of inducing potentially harmful VT during the clinical procedure. Finally, the ability of the RVI maps to identify vulnerable regions with specificity in high resolution computer models could potentially improve the prediction of optimal ablation targets of simulation-based strategies. |
format | Online Article Text |
id | pubmed-6538827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-65388272019-06-03 Characterizing the clinical implementation of a novel activation-repolarization metric to identify targets for catheter ablation of ventricular tachycardias using computational models Campos, Fernando O. Orini, Michele Taggart, Peter Hanson, Ben Lambiase, Pier D. Porter, Bradley Rinaldi, Christopher Aldo Gill, Jaswinder Bishop, Martin J. Comput Biol Med Article Identification of targets for catheter ablation of ventricular tachycardias (VTs) remains a significant challenge. VTs are often driven by re-entrant circuits resulting from a complex interaction between the front (activation) and tail (repolarization) of the electrical wavefront. Most mapping techniques do not take into account the tissue repolarization which may hinder the detection of ablation targets. The re-entry vulnerability index (RVI), a recently proposed mapping procedure, incorporates both activation and repolarization times to uncover VT circuits. The method showed potential in a series of experiments, but it still requires further development to enable its incorporation into a clinical protocol. Here, in-silico experiments were conducted to thoroughly assess RVI maps constructed under clinically-relevant mapping conditions. Within idealized as well as anatomically realistic infarct models, we show that parameters of the algorithm such as the search radius can significantly alter the specificity and sensitivity of the RVI maps. When constructed on sparse grids obtained following various placements of clinical recording catheters, RVI maps can identify vulnerable regions as long as two electrodes were placed on both sides of the line of block. Moreover, maps computed during pacing without inducing VT can reveal areas of abnormal repolarization and slow conduction but not directly vulnerability. In conclusion, the RVI algorithm can detect re-entrant circuits during VT from low resolution mapping grids resembling the clinical setting. Furthermore, RVI maps may provide information about the underlying tissue electrophysiology to guide catheter ablation without the need of inducing potentially harmful VT during the clinical procedure. Finally, the ability of the RVI maps to identify vulnerable regions with specificity in high resolution computer models could potentially improve the prediction of optimal ablation targets of simulation-based strategies. Elsevier 2019-05 /pmc/articles/PMC6538827/ /pubmed/31009930 http://dx.doi.org/10.1016/j.compbiomed.2019.03.018 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Campos, Fernando O. Orini, Michele Taggart, Peter Hanson, Ben Lambiase, Pier D. Porter, Bradley Rinaldi, Christopher Aldo Gill, Jaswinder Bishop, Martin J. Characterizing the clinical implementation of a novel activation-repolarization metric to identify targets for catheter ablation of ventricular tachycardias using computational models |
title | Characterizing the clinical implementation of a novel activation-repolarization metric to identify targets for catheter ablation of ventricular tachycardias using computational models |
title_full | Characterizing the clinical implementation of a novel activation-repolarization metric to identify targets for catheter ablation of ventricular tachycardias using computational models |
title_fullStr | Characterizing the clinical implementation of a novel activation-repolarization metric to identify targets for catheter ablation of ventricular tachycardias using computational models |
title_full_unstemmed | Characterizing the clinical implementation of a novel activation-repolarization metric to identify targets for catheter ablation of ventricular tachycardias using computational models |
title_short | Characterizing the clinical implementation of a novel activation-repolarization metric to identify targets for catheter ablation of ventricular tachycardias using computational models |
title_sort | characterizing the clinical implementation of a novel activation-repolarization metric to identify targets for catheter ablation of ventricular tachycardias using computational models |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538827/ https://www.ncbi.nlm.nih.gov/pubmed/31009930 http://dx.doi.org/10.1016/j.compbiomed.2019.03.018 |
work_keys_str_mv | AT camposfernandoo characterizingtheclinicalimplementationofanovelactivationrepolarizationmetrictoidentifytargetsforcatheterablationofventriculartachycardiasusingcomputationalmodels AT orinimichele characterizingtheclinicalimplementationofanovelactivationrepolarizationmetrictoidentifytargetsforcatheterablationofventriculartachycardiasusingcomputationalmodels AT taggartpeter characterizingtheclinicalimplementationofanovelactivationrepolarizationmetrictoidentifytargetsforcatheterablationofventriculartachycardiasusingcomputationalmodels AT hansonben characterizingtheclinicalimplementationofanovelactivationrepolarizationmetrictoidentifytargetsforcatheterablationofventriculartachycardiasusingcomputationalmodels AT lambiasepierd characterizingtheclinicalimplementationofanovelactivationrepolarizationmetrictoidentifytargetsforcatheterablationofventriculartachycardiasusingcomputationalmodels AT porterbradley characterizingtheclinicalimplementationofanovelactivationrepolarizationmetrictoidentifytargetsforcatheterablationofventriculartachycardiasusingcomputationalmodels AT rinaldichristopheraldo characterizingtheclinicalimplementationofanovelactivationrepolarizationmetrictoidentifytargetsforcatheterablationofventriculartachycardiasusingcomputationalmodels AT gilljaswinder characterizingtheclinicalimplementationofanovelactivationrepolarizationmetrictoidentifytargetsforcatheterablationofventriculartachycardiasusingcomputationalmodels AT bishopmartinj characterizingtheclinicalimplementationofanovelactivationrepolarizationmetrictoidentifytargetsforcatheterablationofventriculartachycardiasusingcomputationalmodels |