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In-vivo validation of a new non-invasive continuous ventricular stroke volume monitoring system in an animal model

INTRODUCTION: Recently, a non-invasive, continuous ventricular stroke volume monitoring system using skin electrodes has been developed. In contrast to impedance-based methods, the new technique (ventricular field recognition) enables measurement of changes in ventricular volume. A prototype using t...

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Autores principales: Konings, Maurits K, Grundeman, Paul F, Goovaerts, Henk G, Roosendaal, Maarten R, Hoefer, Imo E, Doevendans, Pieter A, Rademakers, Frank E, Buhre, Wolfgang F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3387602/
https://www.ncbi.nlm.nih.gov/pubmed/21745380
http://dx.doi.org/10.1186/cc10306
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author Konings, Maurits K
Grundeman, Paul F
Goovaerts, Henk G
Roosendaal, Maarten R
Hoefer, Imo E
Doevendans, Pieter A
Rademakers, Frank E
Buhre, Wolfgang F
author_facet Konings, Maurits K
Grundeman, Paul F
Goovaerts, Henk G
Roosendaal, Maarten R
Hoefer, Imo E
Doevendans, Pieter A
Rademakers, Frank E
Buhre, Wolfgang F
author_sort Konings, Maurits K
collection PubMed
description INTRODUCTION: Recently, a non-invasive, continuous ventricular stroke volume monitoring system using skin electrodes has been developed. In contrast to impedance-based methods, the new technique (ventricular field recognition) enables measurement of changes in ventricular volume. A prototype using this new method was built (the hemologic cardiac profiler, HCP) and validated against a reference method in a pig model during variations in cardiac output. METHODS: In six Dalland pigs, cardiac output was simultaneously measured with the HCP (CO-HCP), and an invasive ultrasonic flow-probe around the ascending aorta (CO-FP). Variations in CO were achieved by change in ventricular loading conditions, cardiac pacing, and dobutamine administration. Data were analysed according to Bland-Altman analysis and Pearson's correlation. RESULTS: Pearson's correlation between the CO-HCP and the CO-FP was r = 0.978. Bland-Altman analysis showed a bias of - 0.114 L/minute, and a variability of the bias (2 standard deviations, 2SD) of 0.55 L/minute. CONCLUSIONS: The results of the present study demonstrate that CO-HCP is comparable to CO-FP in an animal model of cardiac output measurements during a wide variation of CO. Therefore, the HCP has the potential to become a clinical applicable cardiac output monitor.
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spelling pubmed-33876022012-07-02 In-vivo validation of a new non-invasive continuous ventricular stroke volume monitoring system in an animal model Konings, Maurits K Grundeman, Paul F Goovaerts, Henk G Roosendaal, Maarten R Hoefer, Imo E Doevendans, Pieter A Rademakers, Frank E Buhre, Wolfgang F Crit Care Research INTRODUCTION: Recently, a non-invasive, continuous ventricular stroke volume monitoring system using skin electrodes has been developed. In contrast to impedance-based methods, the new technique (ventricular field recognition) enables measurement of changes in ventricular volume. A prototype using this new method was built (the hemologic cardiac profiler, HCP) and validated against a reference method in a pig model during variations in cardiac output. METHODS: In six Dalland pigs, cardiac output was simultaneously measured with the HCP (CO-HCP), and an invasive ultrasonic flow-probe around the ascending aorta (CO-FP). Variations in CO were achieved by change in ventricular loading conditions, cardiac pacing, and dobutamine administration. Data were analysed according to Bland-Altman analysis and Pearson's correlation. RESULTS: Pearson's correlation between the CO-HCP and the CO-FP was r = 0.978. Bland-Altman analysis showed a bias of - 0.114 L/minute, and a variability of the bias (2 standard deviations, 2SD) of 0.55 L/minute. CONCLUSIONS: The results of the present study demonstrate that CO-HCP is comparable to CO-FP in an animal model of cardiac output measurements during a wide variation of CO. Therefore, the HCP has the potential to become a clinical applicable cardiac output monitor. BioMed Central 2011 2011-07-11 /pmc/articles/PMC3387602/ /pubmed/21745380 http://dx.doi.org/10.1186/cc10306 Text en Copyright ©2011 Konings et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Konings, Maurits K
Grundeman, Paul F
Goovaerts, Henk G
Roosendaal, Maarten R
Hoefer, Imo E
Doevendans, Pieter A
Rademakers, Frank E
Buhre, Wolfgang F
In-vivo validation of a new non-invasive continuous ventricular stroke volume monitoring system in an animal model
title In-vivo validation of a new non-invasive continuous ventricular stroke volume monitoring system in an animal model
title_full In-vivo validation of a new non-invasive continuous ventricular stroke volume monitoring system in an animal model
title_fullStr In-vivo validation of a new non-invasive continuous ventricular stroke volume monitoring system in an animal model
title_full_unstemmed In-vivo validation of a new non-invasive continuous ventricular stroke volume monitoring system in an animal model
title_short In-vivo validation of a new non-invasive continuous ventricular stroke volume monitoring system in an animal model
title_sort in-vivo validation of a new non-invasive continuous ventricular stroke volume monitoring system in an animal model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3387602/
https://www.ncbi.nlm.nih.gov/pubmed/21745380
http://dx.doi.org/10.1186/cc10306
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