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Performance comparison of ventricular and arterial dP/dt(max) for assessing left ventricular systolic function during different experimental loading and contractile conditions
BACKGROUND: Maximal left ventricular (LV) pressure rise (LV dP/dt(max)), a classical marker of LV systolic function, requires LV catheterization, thus surrogate arterial pressure waveform measures have been proposed. We compared LV and arterial (femoral and radial) dP/dt(max) to the slope of the LV...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262953/ https://www.ncbi.nlm.nih.gov/pubmed/30486866 http://dx.doi.org/10.1186/s13054-018-2260-1 |
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author | Monge Garcia, Manuel Ignacio Jian, Zhongping Settels, Jos J. Hunley, Charles Cecconi, Maurizio Hatib, Feras Pinsky, Michael R. |
author_facet | Monge Garcia, Manuel Ignacio Jian, Zhongping Settels, Jos J. Hunley, Charles Cecconi, Maurizio Hatib, Feras Pinsky, Michael R. |
author_sort | Monge Garcia, Manuel Ignacio |
collection | PubMed |
description | BACKGROUND: Maximal left ventricular (LV) pressure rise (LV dP/dt(max)), a classical marker of LV systolic function, requires LV catheterization, thus surrogate arterial pressure waveform measures have been proposed. We compared LV and arterial (femoral and radial) dP/dt(max) to the slope of the LV end-systolic pressure-volume relationship (Ees), a load-independent measure of LV contractility, to determine the interactions between dP/dt(max) and Ees as loading and LV contractility varied. METHODS: We measured LV pressure-volume data using a conductance catheter and femoral and radial arterial pressures using a fluid-filled catheter in 10 anesthetized pigs. Ees was calculated as the slope of the end-systolic pressure-volume relationship during a transient inferior vena cava occlusion. Afterload was assessed by the effective arterial elastance. The experimental protocol consisted of sequentially changing afterload (phenylephrine/nitroprusside), preload (bleeding/fluid bolus), and contractility (esmolol/dobutamine). A linear-mixed analysis was used to assess the contribution of cardiac (Ees, end-diastolic volume, effective arterial elastance, heart rate, preload-dependency) and arterial factors (total vascular resistance and arterial compliance) to LV and arterial dP/dt(max). RESULTS: Both LV and arterial dP/dt(max) allowed the tracking of Ees changes, especially during afterload and contractility changes, although arterial dP/dt(max) was lower compared to LV dP/dt(max) (bias 732 ± 539 mmHg⋅s(− 1) for femoral dP/dt(max), and 625 ± 501 mmHg⋅s(− 1) for radial dP/dt(max)). Changes in cardiac contractility (Ees) were the main determinant of LV and arterial dP/dt(max) changes. CONCLUSION: Although arterial dP/dt(max) is a complex function of central and peripheral arterial factors, radial and particularly femoral dP/dt(max) allowed reasonably good tracking of LV contractility changes as loading and inotropic conditions varied. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-018-2260-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6262953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62629532018-12-10 Performance comparison of ventricular and arterial dP/dt(max) for assessing left ventricular systolic function during different experimental loading and contractile conditions Monge Garcia, Manuel Ignacio Jian, Zhongping Settels, Jos J. Hunley, Charles Cecconi, Maurizio Hatib, Feras Pinsky, Michael R. Crit Care Research BACKGROUND: Maximal left ventricular (LV) pressure rise (LV dP/dt(max)), a classical marker of LV systolic function, requires LV catheterization, thus surrogate arterial pressure waveform measures have been proposed. We compared LV and arterial (femoral and radial) dP/dt(max) to the slope of the LV end-systolic pressure-volume relationship (Ees), a load-independent measure of LV contractility, to determine the interactions between dP/dt(max) and Ees as loading and LV contractility varied. METHODS: We measured LV pressure-volume data using a conductance catheter and femoral and radial arterial pressures using a fluid-filled catheter in 10 anesthetized pigs. Ees was calculated as the slope of the end-systolic pressure-volume relationship during a transient inferior vena cava occlusion. Afterload was assessed by the effective arterial elastance. The experimental protocol consisted of sequentially changing afterload (phenylephrine/nitroprusside), preload (bleeding/fluid bolus), and contractility (esmolol/dobutamine). A linear-mixed analysis was used to assess the contribution of cardiac (Ees, end-diastolic volume, effective arterial elastance, heart rate, preload-dependency) and arterial factors (total vascular resistance and arterial compliance) to LV and arterial dP/dt(max). RESULTS: Both LV and arterial dP/dt(max) allowed the tracking of Ees changes, especially during afterload and contractility changes, although arterial dP/dt(max) was lower compared to LV dP/dt(max) (bias 732 ± 539 mmHg⋅s(− 1) for femoral dP/dt(max), and 625 ± 501 mmHg⋅s(− 1) for radial dP/dt(max)). Changes in cardiac contractility (Ees) were the main determinant of LV and arterial dP/dt(max) changes. CONCLUSION: Although arterial dP/dt(max) is a complex function of central and peripheral arterial factors, radial and particularly femoral dP/dt(max) allowed reasonably good tracking of LV contractility changes as loading and inotropic conditions varied. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-018-2260-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-29 /pmc/articles/PMC6262953/ /pubmed/30486866 http://dx.doi.org/10.1186/s13054-018-2260-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Monge Garcia, Manuel Ignacio Jian, Zhongping Settels, Jos J. Hunley, Charles Cecconi, Maurizio Hatib, Feras Pinsky, Michael R. Performance comparison of ventricular and arterial dP/dt(max) for assessing left ventricular systolic function during different experimental loading and contractile conditions |
title | Performance comparison of ventricular and arterial dP/dt(max) for assessing left ventricular systolic function during different experimental loading and contractile conditions |
title_full | Performance comparison of ventricular and arterial dP/dt(max) for assessing left ventricular systolic function during different experimental loading and contractile conditions |
title_fullStr | Performance comparison of ventricular and arterial dP/dt(max) for assessing left ventricular systolic function during different experimental loading and contractile conditions |
title_full_unstemmed | Performance comparison of ventricular and arterial dP/dt(max) for assessing left ventricular systolic function during different experimental loading and contractile conditions |
title_short | Performance comparison of ventricular and arterial dP/dt(max) for assessing left ventricular systolic function during different experimental loading and contractile conditions |
title_sort | performance comparison of ventricular and arterial dp/dt(max) for assessing left ventricular systolic function during different experimental loading and contractile conditions |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262953/ https://www.ncbi.nlm.nih.gov/pubmed/30486866 http://dx.doi.org/10.1186/s13054-018-2260-1 |
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