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Arterial dP/dt(max )accurately reflects left ventricular contractility during shock when adequate vascular filling is achieved

BACKGROUND: Peak first derivative of femoral artery pressure (arterial dP/dt(max)) derived from fluid-filled catheter remains questionable to assess left ventricular (LV) contractility during shock. The aim of this study was to test if arterial dP/dt(max )is reliable for assessing LV contractility d...

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Autores principales: Morimont, Philippe, Lambermont, Bernard, Desaive, Thomas, Janssen, Nathalie, Chase, Geoffrey, D'Orio, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3313844/
https://www.ncbi.nlm.nih.gov/pubmed/22380679
http://dx.doi.org/10.1186/1471-2261-12-13
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author Morimont, Philippe
Lambermont, Bernard
Desaive, Thomas
Janssen, Nathalie
Chase, Geoffrey
D'Orio, Vincent
author_facet Morimont, Philippe
Lambermont, Bernard
Desaive, Thomas
Janssen, Nathalie
Chase, Geoffrey
D'Orio, Vincent
author_sort Morimont, Philippe
collection PubMed
description BACKGROUND: Peak first derivative of femoral artery pressure (arterial dP/dt(max)) derived from fluid-filled catheter remains questionable to assess left ventricular (LV) contractility during shock. The aim of this study was to test if arterial dP/dt(max )is reliable for assessing LV contractility during various hemodynamic conditions such as endotoxin-induced shock and catecholamine infusion. METHODS: Ventricular pressure-volume data obtained with a conductance catheter and invasive arterial pressure obtained with a fluid-filled catheter were continuously recorded in 6 anaesthetized and mechanically ventilated pigs. After a stabilization period, endotoxin was infused to induce shock. Catecholamines were transiently administrated during shock. Arterial dP/dt(max )was compared to end-systolic elastance (Ees), the gold standard method for assessing LV contractility. RESULTS: Endotoxin-induced shock and catecholamine infusion lead to significant variations in LV contractility. Overall, significant correlation (r = 0.51; p < 0.001) but low agreement between the two methods were observed. However, a far better correlation with a good agreement were observed when positive-pressure ventilation induced an arterial pulse pressure variation (PPV) ≤ 11% (r = 0.77; p < 0.001). CONCLUSION: While arterial dP/dt(max )and Ees were significantly correlated during various hemodynamic conditions, arterial dP/dt(max )was more accurate for assessing LV contractility when adequate vascular filling, defined as PPV ≤ 11%, was achieved.
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spelling pubmed-33138442012-03-28 Arterial dP/dt(max )accurately reflects left ventricular contractility during shock when adequate vascular filling is achieved Morimont, Philippe Lambermont, Bernard Desaive, Thomas Janssen, Nathalie Chase, Geoffrey D'Orio, Vincent BMC Cardiovasc Disord Research Article BACKGROUND: Peak first derivative of femoral artery pressure (arterial dP/dt(max)) derived from fluid-filled catheter remains questionable to assess left ventricular (LV) contractility during shock. The aim of this study was to test if arterial dP/dt(max )is reliable for assessing LV contractility during various hemodynamic conditions such as endotoxin-induced shock and catecholamine infusion. METHODS: Ventricular pressure-volume data obtained with a conductance catheter and invasive arterial pressure obtained with a fluid-filled catheter were continuously recorded in 6 anaesthetized and mechanically ventilated pigs. After a stabilization period, endotoxin was infused to induce shock. Catecholamines were transiently administrated during shock. Arterial dP/dt(max )was compared to end-systolic elastance (Ees), the gold standard method for assessing LV contractility. RESULTS: Endotoxin-induced shock and catecholamine infusion lead to significant variations in LV contractility. Overall, significant correlation (r = 0.51; p < 0.001) but low agreement between the two methods were observed. However, a far better correlation with a good agreement were observed when positive-pressure ventilation induced an arterial pulse pressure variation (PPV) ≤ 11% (r = 0.77; p < 0.001). CONCLUSION: While arterial dP/dt(max )and Ees were significantly correlated during various hemodynamic conditions, arterial dP/dt(max )was more accurate for assessing LV contractility when adequate vascular filling, defined as PPV ≤ 11%, was achieved. BioMed Central 2012-03-01 /pmc/articles/PMC3313844/ /pubmed/22380679 http://dx.doi.org/10.1186/1471-2261-12-13 Text en Copyright ©2012 Morimont 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 Article
Morimont, Philippe
Lambermont, Bernard
Desaive, Thomas
Janssen, Nathalie
Chase, Geoffrey
D'Orio, Vincent
Arterial dP/dt(max )accurately reflects left ventricular contractility during shock when adequate vascular filling is achieved
title Arterial dP/dt(max )accurately reflects left ventricular contractility during shock when adequate vascular filling is achieved
title_full Arterial dP/dt(max )accurately reflects left ventricular contractility during shock when adequate vascular filling is achieved
title_fullStr Arterial dP/dt(max )accurately reflects left ventricular contractility during shock when adequate vascular filling is achieved
title_full_unstemmed Arterial dP/dt(max )accurately reflects left ventricular contractility during shock when adequate vascular filling is achieved
title_short Arterial dP/dt(max )accurately reflects left ventricular contractility during shock when adequate vascular filling is achieved
title_sort arterial dp/dt(max )accurately reflects left ventricular contractility during shock when adequate vascular filling is achieved
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3313844/
https://www.ncbi.nlm.nih.gov/pubmed/22380679
http://dx.doi.org/10.1186/1471-2261-12-13
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