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Mechanical ventilation with heliox in an animal model of acute respiratory distress syndrome
BACKGROUND: Heliox has a lower density and higher diffusion capacity compared to oxygen-in-air. We hypothesized that heliox ventilation allows for a reduction in minute volume ventilation and inspiratory pressures needed for adequate gas exchange in an animal model of an acute lung injury. METHODS:...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4513042/ https://www.ncbi.nlm.nih.gov/pubmed/26266912 http://dx.doi.org/10.1186/2197-425X-2-8 |
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author | Beurskens, Charlotte J Aslami, Hamid de Beer, Friso M Roelofs, Joris JTH Vroom, Margreeth B Juffermans, Nicole P |
author_facet | Beurskens, Charlotte J Aslami, Hamid de Beer, Friso M Roelofs, Joris JTH Vroom, Margreeth B Juffermans, Nicole P |
author_sort | Beurskens, Charlotte J |
collection | PubMed |
description | BACKGROUND: Heliox has a lower density and higher diffusion capacity compared to oxygen-in-air. We hypothesized that heliox ventilation allows for a reduction in minute volume ventilation and inspiratory pressures needed for adequate gas exchange in an animal model of an acute lung injury. METHODS: After intratracheal instillation of lipopolysaccharide (10 mg/kg), adult rats were randomized to ventilation with either a gas mixture of helium/oxygen (50:50%) or oxygen/air (50:50%). They were mechanically ventilated according to the ARDSnet recommendations with tidal volumes of 6 ml/kg and monitored with a pneumotachometer. Bronchoalveolar lavage fluid was analyzed for markers of lung injury, and embedded lung sections were histologically scored for lung injury. RESULTS: Heliox limited the increase in driving pressures needed to achieve preset tidal volumes, with a concomitant decrease in loss of compliance. Heliox did neither allow for reduced minute volume ventilation in this model nor improve gas exchange. Also, heliox did not reduce lung injury. CONCLUSIONS: Heliox modestly improved respiratory mechanics but did not improve lung injury in this rat model of acute respiratory distress syndrome. |
format | Online Article Text |
id | pubmed-4513042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-45130422015-07-27 Mechanical ventilation with heliox in an animal model of acute respiratory distress syndrome Beurskens, Charlotte J Aslami, Hamid de Beer, Friso M Roelofs, Joris JTH Vroom, Margreeth B Juffermans, Nicole P Intensive Care Med Exp Research BACKGROUND: Heliox has a lower density and higher diffusion capacity compared to oxygen-in-air. We hypothesized that heliox ventilation allows for a reduction in minute volume ventilation and inspiratory pressures needed for adequate gas exchange in an animal model of an acute lung injury. METHODS: After intratracheal instillation of lipopolysaccharide (10 mg/kg), adult rats were randomized to ventilation with either a gas mixture of helium/oxygen (50:50%) or oxygen/air (50:50%). They were mechanically ventilated according to the ARDSnet recommendations with tidal volumes of 6 ml/kg and monitored with a pneumotachometer. Bronchoalveolar lavage fluid was analyzed for markers of lung injury, and embedded lung sections were histologically scored for lung injury. RESULTS: Heliox limited the increase in driving pressures needed to achieve preset tidal volumes, with a concomitant decrease in loss of compliance. Heliox did neither allow for reduced minute volume ventilation in this model nor improve gas exchange. Also, heliox did not reduce lung injury. CONCLUSIONS: Heliox modestly improved respiratory mechanics but did not improve lung injury in this rat model of acute respiratory distress syndrome. Springer International Publishing 2014-02-06 /pmc/articles/PMC4513042/ /pubmed/26266912 http://dx.doi.org/10.1186/2197-425X-2-8 Text en © Beurskens et al; licensee Springer. 2014 This article is published under license to BioMed Central Ltd. 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 credited. |
spellingShingle | Research Beurskens, Charlotte J Aslami, Hamid de Beer, Friso M Roelofs, Joris JTH Vroom, Margreeth B Juffermans, Nicole P Mechanical ventilation with heliox in an animal model of acute respiratory distress syndrome |
title | Mechanical ventilation with heliox in an animal model of acute respiratory distress syndrome |
title_full | Mechanical ventilation with heliox in an animal model of acute respiratory distress syndrome |
title_fullStr | Mechanical ventilation with heliox in an animal model of acute respiratory distress syndrome |
title_full_unstemmed | Mechanical ventilation with heliox in an animal model of acute respiratory distress syndrome |
title_short | Mechanical ventilation with heliox in an animal model of acute respiratory distress syndrome |
title_sort | mechanical ventilation with heliox in an animal model of acute respiratory distress syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4513042/ https://www.ncbi.nlm.nih.gov/pubmed/26266912 http://dx.doi.org/10.1186/2197-425X-2-8 |
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