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Biophysical Modeling to Determine the Optimization of Left Ventricular Pacing Site and AV/VV Delays in the Acute and Chronic Phase of Cardiac Resynchronization Therapy
BACKGROUND: Cardiac anatomy and function adapt in response to chronic cardiac resynchronization therapy (CRT). The effects of these changes on the optimal left ventricle (LV) lead location and timing delay settings have yet to be fully explored. OBJECTIVE: To predict the effects of chronic CRT on th...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5535003/ https://www.ncbi.nlm.nih.gov/pubmed/27885749 http://dx.doi.org/10.1111/jce.13134 |
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author | LEE, ANGELA W. C. CROZIER, ANDREW HYDE, EOIN R. LAMATA, PABLO TRUONG, MICHAEL SOHAL, MANAV JACKSON, THOMAS BEHAR, JONATHAN M. CLARIDGE, SIMON SHETTY, ANOOP SAMMUT, EVA PLANK, GERNOT RINALDI, CHRISTOPHER ALDO NIEDERER, STEVEN |
author_facet | LEE, ANGELA W. C. CROZIER, ANDREW HYDE, EOIN R. LAMATA, PABLO TRUONG, MICHAEL SOHAL, MANAV JACKSON, THOMAS BEHAR, JONATHAN M. CLARIDGE, SIMON SHETTY, ANOOP SAMMUT, EVA PLANK, GERNOT RINALDI, CHRISTOPHER ALDO NIEDERER, STEVEN |
author_sort | LEE, ANGELA W. C. |
collection | PubMed |
description | BACKGROUND: Cardiac anatomy and function adapt in response to chronic cardiac resynchronization therapy (CRT). The effects of these changes on the optimal left ventricle (LV) lead location and timing delay settings have yet to be fully explored. OBJECTIVE: To predict the effects of chronic CRT on the optimal LV lead location and device timing settings over time. METHODS: Biophysical computational cardiac models were generated for 3 patients, immediately post‐implant (ACUTE) and after at least 6 months of CRT (CHRONIC). Optimal LV pacing area and device settings were predicted by pacing the ACUTE and CHRONIC models across the LV epicardium (49 sites each) with a range of 9 pacing settings and simulating the acute hemodynamic response (AHR) of the heart. RESULTS: There were statistically significant differences between the distribution of the AHR in the ACUTE and CHRONIC models (P < 0.0005 in all cases). The site delivering the maximal AHR shifted location between the ACUTE and CHRONIC models but provided a negligible improvement (<2%). The majority of the acute optimal LV pacing regions (76–100%) and device settings (76–91%) remained optimal chronically. CONCLUSION: Optimization of the LV pacing location and device settings were important at the time of implant, with a reduced benefit over time, where the majority of the acute optimal LV pacing region and device settings remained optimal with chronic CRT. |
format | Online Article Text |
id | pubmed-5535003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55350032017-08-14 Biophysical Modeling to Determine the Optimization of Left Ventricular Pacing Site and AV/VV Delays in the Acute and Chronic Phase of Cardiac Resynchronization Therapy LEE, ANGELA W. C. CROZIER, ANDREW HYDE, EOIN R. LAMATA, PABLO TRUONG, MICHAEL SOHAL, MANAV JACKSON, THOMAS BEHAR, JONATHAN M. CLARIDGE, SIMON SHETTY, ANOOP SAMMUT, EVA PLANK, GERNOT RINALDI, CHRISTOPHER ALDO NIEDERER, STEVEN J Cardiovasc Electrophysiol Original Articles BACKGROUND: Cardiac anatomy and function adapt in response to chronic cardiac resynchronization therapy (CRT). The effects of these changes on the optimal left ventricle (LV) lead location and timing delay settings have yet to be fully explored. OBJECTIVE: To predict the effects of chronic CRT on the optimal LV lead location and device timing settings over time. METHODS: Biophysical computational cardiac models were generated for 3 patients, immediately post‐implant (ACUTE) and after at least 6 months of CRT (CHRONIC). Optimal LV pacing area and device settings were predicted by pacing the ACUTE and CHRONIC models across the LV epicardium (49 sites each) with a range of 9 pacing settings and simulating the acute hemodynamic response (AHR) of the heart. RESULTS: There were statistically significant differences between the distribution of the AHR in the ACUTE and CHRONIC models (P < 0.0005 in all cases). The site delivering the maximal AHR shifted location between the ACUTE and CHRONIC models but provided a negligible improvement (<2%). The majority of the acute optimal LV pacing regions (76–100%) and device settings (76–91%) remained optimal chronically. CONCLUSION: Optimization of the LV pacing location and device settings were important at the time of implant, with a reduced benefit over time, where the majority of the acute optimal LV pacing region and device settings remained optimal with chronic CRT. John Wiley and Sons Inc. 2017-01-14 2017-02 /pmc/articles/PMC5535003/ /pubmed/27885749 http://dx.doi.org/10.1111/jce.13134 Text en © 2016 The Authors Journal of Cardiovascular Electrophysiology Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles LEE, ANGELA W. C. CROZIER, ANDREW HYDE, EOIN R. LAMATA, PABLO TRUONG, MICHAEL SOHAL, MANAV JACKSON, THOMAS BEHAR, JONATHAN M. CLARIDGE, SIMON SHETTY, ANOOP SAMMUT, EVA PLANK, GERNOT RINALDI, CHRISTOPHER ALDO NIEDERER, STEVEN Biophysical Modeling to Determine the Optimization of Left Ventricular Pacing Site and AV/VV Delays in the Acute and Chronic Phase of Cardiac Resynchronization Therapy |
title | Biophysical Modeling to Determine the Optimization of Left Ventricular Pacing Site and AV/VV Delays in the Acute and Chronic Phase of Cardiac Resynchronization Therapy |
title_full | Biophysical Modeling to Determine the Optimization of Left Ventricular Pacing Site and AV/VV Delays in the Acute and Chronic Phase of Cardiac Resynchronization Therapy |
title_fullStr | Biophysical Modeling to Determine the Optimization of Left Ventricular Pacing Site and AV/VV Delays in the Acute and Chronic Phase of Cardiac Resynchronization Therapy |
title_full_unstemmed | Biophysical Modeling to Determine the Optimization of Left Ventricular Pacing Site and AV/VV Delays in the Acute and Chronic Phase of Cardiac Resynchronization Therapy |
title_short | Biophysical Modeling to Determine the Optimization of Left Ventricular Pacing Site and AV/VV Delays in the Acute and Chronic Phase of Cardiac Resynchronization Therapy |
title_sort | biophysical modeling to determine the optimization of left ventricular pacing site and av/vv delays in the acute and chronic phase of cardiac resynchronization therapy |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5535003/ https://www.ncbi.nlm.nih.gov/pubmed/27885749 http://dx.doi.org/10.1111/jce.13134 |
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