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Simultaneous display of multiple three-dimensional electrophysiological datasets (dot mapping)

AIMS: Complex ablation procedures are supported by accurate representation of an increasing variety of electrophysiological and imaging data within electroanatomic mapping systems (EMS). This study aims to develop a novel method for representing multiple complementary datasets on a single cardiac ch...

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Detalles Bibliográficos
Autores principales: Williams, Steven E, Linton, Nick W F, Niederer, Steven, O'Neill, Mark D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834094/
https://www.ncbi.nlm.nih.gov/pubmed/27702855
http://dx.doi.org/10.1093/europace/euw190
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author Williams, Steven E
Linton, Nick W F
Niederer, Steven
O'Neill, Mark D
author_facet Williams, Steven E
Linton, Nick W F
Niederer, Steven
O'Neill, Mark D
author_sort Williams, Steven E
collection PubMed
description AIMS: Complex ablation procedures are supported by accurate representation of an increasing variety of electrophysiological and imaging data within electroanatomic mapping systems (EMS). This study aims to develop a novel method for representing multiple complementary datasets on a single cardiac chamber model. Validation of the system and its application to both atrial and ventricular arrhythmias is examined. METHODS AND RESULTS: Dot mapping was conceived to display multiple datasets by utilizing quantitative surface shading to represent one dataset and finely spaced dots to represent others. Dot positions are randomized within triangular (surface meshes) or tetrahedral (volumetric meshes) simplices making the approach directly transferrable to contemporary EMS. Test data representing uniform electrical activation (n = 10) and focal scarring (n = 10) were used to test dot mapping data perception accuracy. User experience of dot mapping with atrial and ventricular clinical data is evaluated. Dot mapping ensured constant screen dot density for regions of uniform dataset values, regardless of user manipulation of the cardiac chamber. Perception accuracy of dot mapping was equivalent to colour mapping for both propagation direction (1.5 ± 1.8 vs. 4.8 ± 5.3°, P = 0.24) and focal source localization (1.1 ± 0.7 vs. 1.4 ± 0.5 mm, P = 0.88). User acceptance testing revealed equivalent diagnostic accuracy and display fidelity when compared with colour mapping. CONCLUSION: Dot mapping provides the unique ability to display multiple datasets from multiple sources on a single cardiac chamber model. The visual combination of multiple datasets may facilitate interpretation of complex electrophysiological and imaging data.
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spelling pubmed-58340942018-03-07 Simultaneous display of multiple three-dimensional electrophysiological datasets (dot mapping) Williams, Steven E Linton, Nick W F Niederer, Steven O'Neill, Mark D Europace Technical Issues AIMS: Complex ablation procedures are supported by accurate representation of an increasing variety of electrophysiological and imaging data within electroanatomic mapping systems (EMS). This study aims to develop a novel method for representing multiple complementary datasets on a single cardiac chamber model. Validation of the system and its application to both atrial and ventricular arrhythmias is examined. METHODS AND RESULTS: Dot mapping was conceived to display multiple datasets by utilizing quantitative surface shading to represent one dataset and finely spaced dots to represent others. Dot positions are randomized within triangular (surface meshes) or tetrahedral (volumetric meshes) simplices making the approach directly transferrable to contemporary EMS. Test data representing uniform electrical activation (n = 10) and focal scarring (n = 10) were used to test dot mapping data perception accuracy. User experience of dot mapping with atrial and ventricular clinical data is evaluated. Dot mapping ensured constant screen dot density for regions of uniform dataset values, regardless of user manipulation of the cardiac chamber. Perception accuracy of dot mapping was equivalent to colour mapping for both propagation direction (1.5 ± 1.8 vs. 4.8 ± 5.3°, P = 0.24) and focal source localization (1.1 ± 0.7 vs. 1.4 ± 0.5 mm, P = 0.88). User acceptance testing revealed equivalent diagnostic accuracy and display fidelity when compared with colour mapping. CONCLUSION: Dot mapping provides the unique ability to display multiple datasets from multiple sources on a single cardiac chamber model. The visual combination of multiple datasets may facilitate interpretation of complex electrophysiological and imaging data. Oxford University Press 2017-10 2016-10-04 /pmc/articles/PMC5834094/ /pubmed/27702855 http://dx.doi.org/10.1093/europace/euw190 Text en © The Author 2016. Published by Oxford University Press on behalf of the European Society of Cardiology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Technical Issues
Williams, Steven E
Linton, Nick W F
Niederer, Steven
O'Neill, Mark D
Simultaneous display of multiple three-dimensional electrophysiological datasets (dot mapping)
title Simultaneous display of multiple three-dimensional electrophysiological datasets (dot mapping)
title_full Simultaneous display of multiple three-dimensional electrophysiological datasets (dot mapping)
title_fullStr Simultaneous display of multiple three-dimensional electrophysiological datasets (dot mapping)
title_full_unstemmed Simultaneous display of multiple three-dimensional electrophysiological datasets (dot mapping)
title_short Simultaneous display of multiple three-dimensional electrophysiological datasets (dot mapping)
title_sort simultaneous display of multiple three-dimensional electrophysiological datasets (dot mapping)
topic Technical Issues
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834094/
https://www.ncbi.nlm.nih.gov/pubmed/27702855
http://dx.doi.org/10.1093/europace/euw190
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