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Atrial fibrillation source area probability mapping using electrogram patterns of multipole catheters

BACKGROUND: Catheter ablation therapy involving isolation of pulmonary veins (PVs) from the left atrium is performed to terminate atrial fibrillation (AF). Unfortunately, standalone PV isolation procedure has shown to be a suboptimal success with AF continuation or recurrence. One reason, especially...

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Autores principales: Ganesan, Prasanth, Cherry, Elizabeth M., Huang, David T., Pertsov, Arkady M., Ghoraani, Behnaz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201756/
https://www.ncbi.nlm.nih.gov/pubmed/32370754
http://dx.doi.org/10.1186/s12938-020-00769-0
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author Ganesan, Prasanth
Cherry, Elizabeth M.
Huang, David T.
Pertsov, Arkady M.
Ghoraani, Behnaz
author_facet Ganesan, Prasanth
Cherry, Elizabeth M.
Huang, David T.
Pertsov, Arkady M.
Ghoraani, Behnaz
author_sort Ganesan, Prasanth
collection PubMed
description BACKGROUND: Catheter ablation therapy involving isolation of pulmonary veins (PVs) from the left atrium is performed to terminate atrial fibrillation (AF). Unfortunately, standalone PV isolation procedure has shown to be a suboptimal success with AF continuation or recurrence. One reason, especially in patients with persistent or high-burden paroxysmal AF, is known to be due to the formation of repeating-pattern AF sources with a meandering core inside the atria. However, there is a need for accurate mapping and localization of these sources during catheter ablation. METHODS: A novel AF source area probability (ASAP) mapping algorithm was developed and evaluated in 2D and 3D atrial simulated tissues with various arrhythmia scenarios and a retrospective study with three cases of clinical human AF. The ASAP mapping analyzes the electrograms collected from a multipole diagnostic catheter that is commonly used during catheter ablation procedure to intelligently sample the atria and delineate the trajectory path of a meandering repeating-pattern AF source. ASAP starts by placing the diagnostic catheter at an arbitrary location in the atria. It analyzes the recorded bipolar electrograms to build an ASAP map over the atrium anatomy and suggests an optimal location for the subsequent catheter location. ASAP then determines from the constructed ASAP map if an AF source has been delineated. If so, the catheter navigation is stopped and the algorithm provides the area of the AF source. Otherwise, the catheter is navigated to the suggested location, and the process is continued until an AF-source area is delineated. RESULTS: ASAP delineated the AF source in over 95% of the simulated human AF cases within less than eight catheter placements regardless of the initial catheter placement. The success of ASAP in the clinical AF was confirmed by the ablation outcomes and the electrogram patterns at the delineated area. CONCLUSION: Our analysis indicates the potential of the ASAP mapping to provide accurate information about the area of the meandering repeating-pattern AF sources as AF ablation targets for effective AF termination. Our algorithm could improve the success of AF catheter ablation therapy by locating and subsequently targeting patient-specific and repeating-pattern AF sources inside the atria.
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spelling pubmed-72017562020-05-08 Atrial fibrillation source area probability mapping using electrogram patterns of multipole catheters Ganesan, Prasanth Cherry, Elizabeth M. Huang, David T. Pertsov, Arkady M. Ghoraani, Behnaz Biomed Eng Online Research BACKGROUND: Catheter ablation therapy involving isolation of pulmonary veins (PVs) from the left atrium is performed to terminate atrial fibrillation (AF). Unfortunately, standalone PV isolation procedure has shown to be a suboptimal success with AF continuation or recurrence. One reason, especially in patients with persistent or high-burden paroxysmal AF, is known to be due to the formation of repeating-pattern AF sources with a meandering core inside the atria. However, there is a need for accurate mapping and localization of these sources during catheter ablation. METHODS: A novel AF source area probability (ASAP) mapping algorithm was developed and evaluated in 2D and 3D atrial simulated tissues with various arrhythmia scenarios and a retrospective study with three cases of clinical human AF. The ASAP mapping analyzes the electrograms collected from a multipole diagnostic catheter that is commonly used during catheter ablation procedure to intelligently sample the atria and delineate the trajectory path of a meandering repeating-pattern AF source. ASAP starts by placing the diagnostic catheter at an arbitrary location in the atria. It analyzes the recorded bipolar electrograms to build an ASAP map over the atrium anatomy and suggests an optimal location for the subsequent catheter location. ASAP then determines from the constructed ASAP map if an AF source has been delineated. If so, the catheter navigation is stopped and the algorithm provides the area of the AF source. Otherwise, the catheter is navigated to the suggested location, and the process is continued until an AF-source area is delineated. RESULTS: ASAP delineated the AF source in over 95% of the simulated human AF cases within less than eight catheter placements regardless of the initial catheter placement. The success of ASAP in the clinical AF was confirmed by the ablation outcomes and the electrogram patterns at the delineated area. CONCLUSION: Our analysis indicates the potential of the ASAP mapping to provide accurate information about the area of the meandering repeating-pattern AF sources as AF ablation targets for effective AF termination. Our algorithm could improve the success of AF catheter ablation therapy by locating and subsequently targeting patient-specific and repeating-pattern AF sources inside the atria. BioMed Central 2020-05-05 /pmc/articles/PMC7201756/ /pubmed/32370754 http://dx.doi.org/10.1186/s12938-020-00769-0 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ganesan, Prasanth
Cherry, Elizabeth M.
Huang, David T.
Pertsov, Arkady M.
Ghoraani, Behnaz
Atrial fibrillation source area probability mapping using electrogram patterns of multipole catheters
title Atrial fibrillation source area probability mapping using electrogram patterns of multipole catheters
title_full Atrial fibrillation source area probability mapping using electrogram patterns of multipole catheters
title_fullStr Atrial fibrillation source area probability mapping using electrogram patterns of multipole catheters
title_full_unstemmed Atrial fibrillation source area probability mapping using electrogram patterns of multipole catheters
title_short Atrial fibrillation source area probability mapping using electrogram patterns of multipole catheters
title_sort atrial fibrillation source area probability mapping using electrogram patterns of multipole catheters
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201756/
https://www.ncbi.nlm.nih.gov/pubmed/32370754
http://dx.doi.org/10.1186/s12938-020-00769-0
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