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Longitudinal Validation of Right Ventricular Pressure Monitoring for the Assessment of Right Ventricular Systolic Dysfunction in a Large Animal Ischemic Model
Right ventricular (RV) dysfunction is a major cause of morbidity and mortality in intensive care and cardiac surgery. Early detection of RV dysfunction may be facilitated by continuous monitoring of RV waveform obtained from a pulmonary artery catheter. The objective is to evaluate the extent to whi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9851694/ https://www.ncbi.nlm.nih.gov/pubmed/36699251 http://dx.doi.org/10.1097/CCE.0000000000000847 |
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author | Couture, Etienne J. Moses, Kevin Monge García, Manuel Ignacio Potes, Cristhian Haddad, Francois Grønlykke, Lars Garcia, Fernando Paster, Eden Pibarot, Philippe Denault, André Y. |
author_facet | Couture, Etienne J. Moses, Kevin Monge García, Manuel Ignacio Potes, Cristhian Haddad, Francois Grønlykke, Lars Garcia, Fernando Paster, Eden Pibarot, Philippe Denault, André Y. |
author_sort | Couture, Etienne J. |
collection | PubMed |
description | Right ventricular (RV) dysfunction is a major cause of morbidity and mortality in intensive care and cardiac surgery. Early detection of RV dysfunction may be facilitated by continuous monitoring of RV waveform obtained from a pulmonary artery catheter. The objective is to evaluate the extent to which RV pressure monitoring can detect changes in RV systolic performance assess by RV end-systolic elastance (E(es)) following the development of an acute RV ischemic in a porcine model. HYPOTHESIS: RV pressure monitoring can detect changes in RV systolic performance assess by RV E(es) following the development of an acute RV ischemic model. METHODS AND MODELS: Acute ischemic RV dysfunction was induced by progressive embolization of microsphere in the right coronary artery to mimic RV dysfunction clinically experienced during cardiopulmonary bypass separation caused by air microemboli. RV hemodynamic performance was assessed using RV pressure waveform-derived parameters and RV E(es) obtained using a conductance catheter during inferior vena cava occlusions. RESULTS: Acute ischemia resulted in a significant reduction in RV E(es) from 0.26 mm Hg/mL (interquartile range, 0.16–0.32 mm Hg/mL) to 0.14 mm Hg/mL (0.11–0.19 mm Hg/mL; p < 0.010), cardiac output from 6.3 L/min (5.7–7 L/min) to 4.5 (3.9–5.2 L/min; p = 0.007), mean systemic arterial pressure from 72 mm Hg (66–74 mm Hg) to 51 mm Hg (46–56 mm Hg; p < 0.001), and mixed venous oxygen saturation from 65% (57–72%) to 41% (35–45%; p < 0.001). Linear mixed-effect model analysis was used to assess the relationship between E(es) and RV pressure-derived parameters. The reduction in RV E(es) best correlated with a reduction in RV maximum first derivative of pressure during isovolumetric contraction (dP/dt(max)) and single-beat RV E(es). Adjusting RV dP/dt(max) for heart rate resulted in an improved surrogate of RV E(es). INTERPRETATION AND CONCLUSIONS: Stepwise decreases in RV E(es) during acute ischemic RV dysfunction were accurately tracked by RV dP/dt(max) derived from the RV pressure waveform. |
format | Online Article Text |
id | pubmed-9851694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-98516942023-01-24 Longitudinal Validation of Right Ventricular Pressure Monitoring for the Assessment of Right Ventricular Systolic Dysfunction in a Large Animal Ischemic Model Couture, Etienne J. Moses, Kevin Monge García, Manuel Ignacio Potes, Cristhian Haddad, Francois Grønlykke, Lars Garcia, Fernando Paster, Eden Pibarot, Philippe Denault, André Y. Crit Care Explor Original Basic Science Report Right ventricular (RV) dysfunction is a major cause of morbidity and mortality in intensive care and cardiac surgery. Early detection of RV dysfunction may be facilitated by continuous monitoring of RV waveform obtained from a pulmonary artery catheter. The objective is to evaluate the extent to which RV pressure monitoring can detect changes in RV systolic performance assess by RV end-systolic elastance (E(es)) following the development of an acute RV ischemic in a porcine model. HYPOTHESIS: RV pressure monitoring can detect changes in RV systolic performance assess by RV E(es) following the development of an acute RV ischemic model. METHODS AND MODELS: Acute ischemic RV dysfunction was induced by progressive embolization of microsphere in the right coronary artery to mimic RV dysfunction clinically experienced during cardiopulmonary bypass separation caused by air microemboli. RV hemodynamic performance was assessed using RV pressure waveform-derived parameters and RV E(es) obtained using a conductance catheter during inferior vena cava occlusions. RESULTS: Acute ischemia resulted in a significant reduction in RV E(es) from 0.26 mm Hg/mL (interquartile range, 0.16–0.32 mm Hg/mL) to 0.14 mm Hg/mL (0.11–0.19 mm Hg/mL; p < 0.010), cardiac output from 6.3 L/min (5.7–7 L/min) to 4.5 (3.9–5.2 L/min; p = 0.007), mean systemic arterial pressure from 72 mm Hg (66–74 mm Hg) to 51 mm Hg (46–56 mm Hg; p < 0.001), and mixed venous oxygen saturation from 65% (57–72%) to 41% (35–45%; p < 0.001). Linear mixed-effect model analysis was used to assess the relationship between E(es) and RV pressure-derived parameters. The reduction in RV E(es) best correlated with a reduction in RV maximum first derivative of pressure during isovolumetric contraction (dP/dt(max)) and single-beat RV E(es). Adjusting RV dP/dt(max) for heart rate resulted in an improved surrogate of RV E(es). INTERPRETATION AND CONCLUSIONS: Stepwise decreases in RV E(es) during acute ischemic RV dysfunction were accurately tracked by RV dP/dt(max) derived from the RV pressure waveform. Lippincott Williams & Wilkins 2023-01-18 /pmc/articles/PMC9851694/ /pubmed/36699251 http://dx.doi.org/10.1097/CCE.0000000000000847 Text en Copyright © 2023 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of the Society of Critical Care Medicine. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Original Basic Science Report Couture, Etienne J. Moses, Kevin Monge García, Manuel Ignacio Potes, Cristhian Haddad, Francois Grønlykke, Lars Garcia, Fernando Paster, Eden Pibarot, Philippe Denault, André Y. Longitudinal Validation of Right Ventricular Pressure Monitoring for the Assessment of Right Ventricular Systolic Dysfunction in a Large Animal Ischemic Model |
title | Longitudinal Validation of Right Ventricular Pressure Monitoring for the Assessment of Right Ventricular Systolic Dysfunction in a Large Animal Ischemic Model |
title_full | Longitudinal Validation of Right Ventricular Pressure Monitoring for the Assessment of Right Ventricular Systolic Dysfunction in a Large Animal Ischemic Model |
title_fullStr | Longitudinal Validation of Right Ventricular Pressure Monitoring for the Assessment of Right Ventricular Systolic Dysfunction in a Large Animal Ischemic Model |
title_full_unstemmed | Longitudinal Validation of Right Ventricular Pressure Monitoring for the Assessment of Right Ventricular Systolic Dysfunction in a Large Animal Ischemic Model |
title_short | Longitudinal Validation of Right Ventricular Pressure Monitoring for the Assessment of Right Ventricular Systolic Dysfunction in a Large Animal Ischemic Model |
title_sort | longitudinal validation of right ventricular pressure monitoring for the assessment of right ventricular systolic dysfunction in a large animal ischemic model |
topic | Original Basic Science Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9851694/ https://www.ncbi.nlm.nih.gov/pubmed/36699251 http://dx.doi.org/10.1097/CCE.0000000000000847 |
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