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Effect of positive end-expiratory pressure and tidal volume on lung injury induced by alveolar instability

INTRODUCTION: One potential mechanism of ventilator-induced lung injury (VILI) is due to shear stresses associated with alveolar instability (recruitment/derecruitment). It has been postulated that the optimal combination of tidal volume (Vt) and positive end-expiratory pressure (PEEP) stabilizes al...

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Autores principales: Halter, Jeffrey M, Steinberg, Jay M, Gatto, Louis A, DiRocco, Joseph D, Pavone, Lucio A, Schiller, Henry J, Albert, Scott, Lee, Hsi-Ming, Carney, David, Nieman, Gary F
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151879/
https://www.ncbi.nlm.nih.gov/pubmed/17302983
http://dx.doi.org/10.1186/cc5695
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author Halter, Jeffrey M
Steinberg, Jay M
Gatto, Louis A
DiRocco, Joseph D
Pavone, Lucio A
Schiller, Henry J
Albert, Scott
Lee, Hsi-Ming
Carney, David
Nieman, Gary F
author_facet Halter, Jeffrey M
Steinberg, Jay M
Gatto, Louis A
DiRocco, Joseph D
Pavone, Lucio A
Schiller, Henry J
Albert, Scott
Lee, Hsi-Ming
Carney, David
Nieman, Gary F
author_sort Halter, Jeffrey M
collection PubMed
description INTRODUCTION: One potential mechanism of ventilator-induced lung injury (VILI) is due to shear stresses associated with alveolar instability (recruitment/derecruitment). It has been postulated that the optimal combination of tidal volume (Vt) and positive end-expiratory pressure (PEEP) stabilizes alveoli, thus diminishing recruitment/derecruitment and reducing VILI. In this study we directly visualized the effect of Vt and PEEP on alveolar mechanics and correlated alveolar stability with lung injury. METHODS: In vivo microscopy was utilized in a surfactant deactivation porcine ARDS model to observe the effects of Vt and PEEP on alveolar mechanics. In phase I (n = 3), nine combinations of Vt and PEEP were evaluated to determine which combination resulted in the most and least alveolar instability. In phase II (n = 6), data from phase I were utilized to separate animals into two groups based on the combination of Vt and PEEP that caused the most alveolar stability (high Vt [15 cc/kg] plus low PEEP [5 cmH(2)O]) and least alveolar stability (low Vt [6 cc/kg] and plus PEEP [20 cmH(2)O]). The animals were ventilated for three hours following lung injury, with in vivo alveolar stability measured and VILI assessed by lung function, blood gases, morphometrically, and by changes in inflammatory mediators. RESULTS: High Vt/low PEEP resulted in the most alveolar instability and lung injury, as indicated by lung function and morphometric analysis of lung tissue. Low Vt/high PEEP stabilized alveoli, improved oxygenation, and reduced lung injury. There were no significant differences between groups in plasma or bronchoalveolar lavage cytokines or proteases. CONCLUSION: A ventilatory strategy employing high Vt and low PEEP causes alveolar instability, and to our knowledge this is the first study to confirm this finding by direct visualization. These studies demonstrate that low Vt and high PEEP work synergistically to stabilize alveoli, although increased PEEP is more effective at stabilizing alveoli than reduced Vt. In this animal model of ARDS, alveolar instability results in lung injury (VILI) with minimal changes in plasma and bronchoalveolar lavage cytokines and proteases. This suggests that the mechanism of lung injury in the high Vt/low PEEP group was mechanical, not inflammatory in nature.
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spelling pubmed-21518792007-12-25 Effect of positive end-expiratory pressure and tidal volume on lung injury induced by alveolar instability Halter, Jeffrey M Steinberg, Jay M Gatto, Louis A DiRocco, Joseph D Pavone, Lucio A Schiller, Henry J Albert, Scott Lee, Hsi-Ming Carney, David Nieman, Gary F Crit Care Research INTRODUCTION: One potential mechanism of ventilator-induced lung injury (VILI) is due to shear stresses associated with alveolar instability (recruitment/derecruitment). It has been postulated that the optimal combination of tidal volume (Vt) and positive end-expiratory pressure (PEEP) stabilizes alveoli, thus diminishing recruitment/derecruitment and reducing VILI. In this study we directly visualized the effect of Vt and PEEP on alveolar mechanics and correlated alveolar stability with lung injury. METHODS: In vivo microscopy was utilized in a surfactant deactivation porcine ARDS model to observe the effects of Vt and PEEP on alveolar mechanics. In phase I (n = 3), nine combinations of Vt and PEEP were evaluated to determine which combination resulted in the most and least alveolar instability. In phase II (n = 6), data from phase I were utilized to separate animals into two groups based on the combination of Vt and PEEP that caused the most alveolar stability (high Vt [15 cc/kg] plus low PEEP [5 cmH(2)O]) and least alveolar stability (low Vt [6 cc/kg] and plus PEEP [20 cmH(2)O]). The animals were ventilated for three hours following lung injury, with in vivo alveolar stability measured and VILI assessed by lung function, blood gases, morphometrically, and by changes in inflammatory mediators. RESULTS: High Vt/low PEEP resulted in the most alveolar instability and lung injury, as indicated by lung function and morphometric analysis of lung tissue. Low Vt/high PEEP stabilized alveoli, improved oxygenation, and reduced lung injury. There were no significant differences between groups in plasma or bronchoalveolar lavage cytokines or proteases. CONCLUSION: A ventilatory strategy employing high Vt and low PEEP causes alveolar instability, and to our knowledge this is the first study to confirm this finding by direct visualization. These studies demonstrate that low Vt and high PEEP work synergistically to stabilize alveoli, although increased PEEP is more effective at stabilizing alveoli than reduced Vt. In this animal model of ARDS, alveolar instability results in lung injury (VILI) with minimal changes in plasma and bronchoalveolar lavage cytokines and proteases. This suggests that the mechanism of lung injury in the high Vt/low PEEP group was mechanical, not inflammatory in nature. BioMed Central 2007 2007-02-15 /pmc/articles/PMC2151879/ /pubmed/17302983 http://dx.doi.org/10.1186/cc5695 Text en Copyright © 2007 Halter 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
Halter, Jeffrey M
Steinberg, Jay M
Gatto, Louis A
DiRocco, Joseph D
Pavone, Lucio A
Schiller, Henry J
Albert, Scott
Lee, Hsi-Ming
Carney, David
Nieman, Gary F
Effect of positive end-expiratory pressure and tidal volume on lung injury induced by alveolar instability
title Effect of positive end-expiratory pressure and tidal volume on lung injury induced by alveolar instability
title_full Effect of positive end-expiratory pressure and tidal volume on lung injury induced by alveolar instability
title_fullStr Effect of positive end-expiratory pressure and tidal volume on lung injury induced by alveolar instability
title_full_unstemmed Effect of positive end-expiratory pressure and tidal volume on lung injury induced by alveolar instability
title_short Effect of positive end-expiratory pressure and tidal volume on lung injury induced by alveolar instability
title_sort effect of positive end-expiratory pressure and tidal volume on lung injury induced by alveolar instability
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151879/
https://www.ncbi.nlm.nih.gov/pubmed/17302983
http://dx.doi.org/10.1186/cc5695
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