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The relative role of patient physiology and device optimisation in cardiac resynchronisation therapy: A computational modelling study

Cardiac resynchronisation therapy (CRT) is an established treatment for heart failure, however the effective selection of patients and optimisation of therapy remain controversial. While extensive research is ongoing, it remains unclear whether improvements in patient selection or therapy planning o...

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Autores principales: Crozier, Andrew, Blazevic, Bojan, Lamata, Pablo, Plank, Gernot, Ginks, Matthew, Duckett, Simon, Sohal, Manav, Shetty, Anoop, Rinaldi, Christopher A., Razavi, Reza, Smith, Nicolas P., Niederer, Steven A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4915816/
https://www.ncbi.nlm.nih.gov/pubmed/26546827
http://dx.doi.org/10.1016/j.yjmcc.2015.10.026
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author Crozier, Andrew
Blazevic, Bojan
Lamata, Pablo
Plank, Gernot
Ginks, Matthew
Duckett, Simon
Sohal, Manav
Shetty, Anoop
Rinaldi, Christopher A.
Razavi, Reza
Smith, Nicolas P.
Niederer, Steven A.
author_facet Crozier, Andrew
Blazevic, Bojan
Lamata, Pablo
Plank, Gernot
Ginks, Matthew
Duckett, Simon
Sohal, Manav
Shetty, Anoop
Rinaldi, Christopher A.
Razavi, Reza
Smith, Nicolas P.
Niederer, Steven A.
author_sort Crozier, Andrew
collection PubMed
description Cardiac resynchronisation therapy (CRT) is an established treatment for heart failure, however the effective selection of patients and optimisation of therapy remain controversial. While extensive research is ongoing, it remains unclear whether improvements in patient selection or therapy planning offers a greater opportunity for the improvement of clinical outcomes. This computational study investigates the impact of both physiological conditions that guide patient selection and the optimisation of pacing lead placement on CRT outcomes. A multi-scale biophysical model of cardiac electromechanics was developed and personalised to patient data in three patients. These models were separated into components representing cardiac anatomy, pacing lead location, myocardial conductivity and stiffness, afterload, active contraction and conduction block for each individual, and recombined to generate a cohort of 648 virtual patients. The effect of these components on the change in total activation time of the ventricles (ΔTAT) and acute haemodynamic response (AHR) was analysed. The pacing site location was found to have the largest effect on ΔTAT and AHR. Secondary effects on ΔTAT and AHR were found for functional conduction block and cardiac anatomy. The simulation results highlight a need for a greater emphasis on therapy optimisation in order to achieve the best outcomes for patients.
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spelling pubmed-49158162016-07-01 The relative role of patient physiology and device optimisation in cardiac resynchronisation therapy: A computational modelling study Crozier, Andrew Blazevic, Bojan Lamata, Pablo Plank, Gernot Ginks, Matthew Duckett, Simon Sohal, Manav Shetty, Anoop Rinaldi, Christopher A. Razavi, Reza Smith, Nicolas P. Niederer, Steven A. J Mol Cell Cardiol Review Article Cardiac resynchronisation therapy (CRT) is an established treatment for heart failure, however the effective selection of patients and optimisation of therapy remain controversial. While extensive research is ongoing, it remains unclear whether improvements in patient selection or therapy planning offers a greater opportunity for the improvement of clinical outcomes. This computational study investigates the impact of both physiological conditions that guide patient selection and the optimisation of pacing lead placement on CRT outcomes. A multi-scale biophysical model of cardiac electromechanics was developed and personalised to patient data in three patients. These models were separated into components representing cardiac anatomy, pacing lead location, myocardial conductivity and stiffness, afterload, active contraction and conduction block for each individual, and recombined to generate a cohort of 648 virtual patients. The effect of these components on the change in total activation time of the ventricles (ΔTAT) and acute haemodynamic response (AHR) was analysed. The pacing site location was found to have the largest effect on ΔTAT and AHR. Secondary effects on ΔTAT and AHR were found for functional conduction block and cardiac anatomy. The simulation results highlight a need for a greater emphasis on therapy optimisation in order to achieve the best outcomes for patients. Academic Press 2016-07 /pmc/articles/PMC4915816/ /pubmed/26546827 http://dx.doi.org/10.1016/j.yjmcc.2015.10.026 Text en © 2015 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 Review Article
Crozier, Andrew
Blazevic, Bojan
Lamata, Pablo
Plank, Gernot
Ginks, Matthew
Duckett, Simon
Sohal, Manav
Shetty, Anoop
Rinaldi, Christopher A.
Razavi, Reza
Smith, Nicolas P.
Niederer, Steven A.
The relative role of patient physiology and device optimisation in cardiac resynchronisation therapy: A computational modelling study
title The relative role of patient physiology and device optimisation in cardiac resynchronisation therapy: A computational modelling study
title_full The relative role of patient physiology and device optimisation in cardiac resynchronisation therapy: A computational modelling study
title_fullStr The relative role of patient physiology and device optimisation in cardiac resynchronisation therapy: A computational modelling study
title_full_unstemmed The relative role of patient physiology and device optimisation in cardiac resynchronisation therapy: A computational modelling study
title_short The relative role of patient physiology and device optimisation in cardiac resynchronisation therapy: A computational modelling study
title_sort relative role of patient physiology and device optimisation in cardiac resynchronisation therapy: a computational modelling study
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4915816/
https://www.ncbi.nlm.nih.gov/pubmed/26546827
http://dx.doi.org/10.1016/j.yjmcc.2015.10.026
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