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Impact of anatomical reverse remodelling in the design of optimal quadripolar pacing leads: A computational study

Lead position is an important factor in determining response to Cardiac Resynchronization Therapy (CRT) in dyssynchronous heart failure (HF) patients. Multipoint pacing (MPP) enables pacing from multiple electrodes within the same lead, improving the potential outcome for patients. Virtual quadripol...

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Autores principales: Rodero, Cristobal, Strocchi, Marina, Lee, Angela W.C., Rinaldi, Christopher A., Vigmond, Edward J., Plank, Gernot, Lamata, Pablo, Niederer, Steven A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752960/
https://www.ncbi.nlm.nih.gov/pubmed/34852973
http://dx.doi.org/10.1016/j.compbiomed.2021.105073
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author Rodero, Cristobal
Strocchi, Marina
Lee, Angela W.C.
Rinaldi, Christopher A.
Vigmond, Edward J.
Plank, Gernot
Lamata, Pablo
Niederer, Steven A.
author_facet Rodero, Cristobal
Strocchi, Marina
Lee, Angela W.C.
Rinaldi, Christopher A.
Vigmond, Edward J.
Plank, Gernot
Lamata, Pablo
Niederer, Steven A.
author_sort Rodero, Cristobal
collection PubMed
description Lead position is an important factor in determining response to Cardiac Resynchronization Therapy (CRT) in dyssynchronous heart failure (HF) patients. Multipoint pacing (MPP) enables pacing from multiple electrodes within the same lead, improving the potential outcome for patients. Virtual quadripolar lead designs were evaluated by simulating pacing from all combinations of 1 and 2 electrodes along the lead in each virtual patient from cohorts of HF (n = 24) and simulated reverse remodelled (RR, n = 20) patients. Electrical synchrony was assessed by the time 90% of the ventricular myocardium is activated (AT090). Optimal 1 and 2 electrode pacing configurations for AT090 were combined to identify the 4-electrode lead design that maximised benefits across all patients. LV pacing in the HF cohort in all possible single and double electrode locations reduced AT090 by 14.48 ± 5.01 ms (11.92 ± 3.51%). The major determinant of reduction in activation time was patient anatomy. Pacing with a single optimal lead design reduced AT090 more in the HF cohort than the RR cohort (12.68 ± 3.29% vs 10.81 ± 2.34%). Pacing with a single combined HF and RR population-optimised lead design achieves electrical resynchronization with near equivalence to personalised lead designs both in HF and RR anatomies. These findings suggest that although lead configurations have to be tailored to each patient, a single optimal lead design is sufficient to obtain near-optimal results across most patients. This study shows the potential of virtual clinical trials as tools to compare existing and explore new lead designs.
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spelling pubmed-87529602022-01-19 Impact of anatomical reverse remodelling in the design of optimal quadripolar pacing leads: A computational study Rodero, Cristobal Strocchi, Marina Lee, Angela W.C. Rinaldi, Christopher A. Vigmond, Edward J. Plank, Gernot Lamata, Pablo Niederer, Steven A. Comput Biol Med Article Lead position is an important factor in determining response to Cardiac Resynchronization Therapy (CRT) in dyssynchronous heart failure (HF) patients. Multipoint pacing (MPP) enables pacing from multiple electrodes within the same lead, improving the potential outcome for patients. Virtual quadripolar lead designs were evaluated by simulating pacing from all combinations of 1 and 2 electrodes along the lead in each virtual patient from cohorts of HF (n = 24) and simulated reverse remodelled (RR, n = 20) patients. Electrical synchrony was assessed by the time 90% of the ventricular myocardium is activated (AT090). Optimal 1 and 2 electrode pacing configurations for AT090 were combined to identify the 4-electrode lead design that maximised benefits across all patients. LV pacing in the HF cohort in all possible single and double electrode locations reduced AT090 by 14.48 ± 5.01 ms (11.92 ± 3.51%). The major determinant of reduction in activation time was patient anatomy. Pacing with a single optimal lead design reduced AT090 more in the HF cohort than the RR cohort (12.68 ± 3.29% vs 10.81 ± 2.34%). Pacing with a single combined HF and RR population-optimised lead design achieves electrical resynchronization with near equivalence to personalised lead designs both in HF and RR anatomies. These findings suggest that although lead configurations have to be tailored to each patient, a single optimal lead design is sufficient to obtain near-optimal results across most patients. This study shows the potential of virtual clinical trials as tools to compare existing and explore new lead designs. Elsevier 2022-01 /pmc/articles/PMC8752960/ /pubmed/34852973 http://dx.doi.org/10.1016/j.compbiomed.2021.105073 Text en © 2021 The Authors https://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
Rodero, Cristobal
Strocchi, Marina
Lee, Angela W.C.
Rinaldi, Christopher A.
Vigmond, Edward J.
Plank, Gernot
Lamata, Pablo
Niederer, Steven A.
Impact of anatomical reverse remodelling in the design of optimal quadripolar pacing leads: A computational study
title Impact of anatomical reverse remodelling in the design of optimal quadripolar pacing leads: A computational study
title_full Impact of anatomical reverse remodelling in the design of optimal quadripolar pacing leads: A computational study
title_fullStr Impact of anatomical reverse remodelling in the design of optimal quadripolar pacing leads: A computational study
title_full_unstemmed Impact of anatomical reverse remodelling in the design of optimal quadripolar pacing leads: A computational study
title_short Impact of anatomical reverse remodelling in the design of optimal quadripolar pacing leads: A computational study
title_sort impact of anatomical reverse remodelling in the design of optimal quadripolar pacing leads: a computational study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752960/
https://www.ncbi.nlm.nih.gov/pubmed/34852973
http://dx.doi.org/10.1016/j.compbiomed.2021.105073
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