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Systemic oxygen delivery by peritoneal perfusion of oxygen microbubbles
Severe hypoxemia refractory to pulmonary mechanical ventilation remains life-threatening in critically ill patients. Peritoneal ventilation has long been desired for extrapulmonary oxygenation owing to easy access of the peritoneal cavity for catheterization and the relative safety compared to an ex...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7124456/ https://www.ncbi.nlm.nih.gov/pubmed/24439406 http://dx.doi.org/10.1016/j.biomaterials.2013.12.070 |
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author | Feshitan, Jameel A. Legband, Nathan D. Borden, Mark A. Terry, Benjamin S. |
author_facet | Feshitan, Jameel A. Legband, Nathan D. Borden, Mark A. Terry, Benjamin S. |
author_sort | Feshitan, Jameel A. |
collection | PubMed |
description | Severe hypoxemia refractory to pulmonary mechanical ventilation remains life-threatening in critically ill patients. Peritoneal ventilation has long been desired for extrapulmonary oxygenation owing to easy access of the peritoneal cavity for catheterization and the relative safety compared to an extracorporeal circuit. Unfortunately, prior attempts involving direct oxygen ventilation or aqueous perfusates of fluorocarbons or hemoglobin carriers have failed, leading many researchers to abandon the method. We attribute these prior failures to limited mass transfer of oxygen to the peritoneum and have designed an oxygen formulation that overcomes this limitation. Using phospholipid-coated oxygen microbubbles (OMBs), we demonstrate 100% survival for rats experiencing acute lung trauma to at least 2 h. In contrast, all untreated rats and rats treated with peritoneal oxygenated saline died within 30 min. For rats treated with OMBs, hemoglobin saturation and heart rate were at normal levels over the 2-h timeframe. Peritoneal oxygenation with OMBs was therefore shown to be safe and effective, and the method requires less equipment and technical expertise than initiating and maintaining an extracorporeal circuit. Further translation of peritoneal oxygenation with OMBs may provide therapy for acute respiratory distress syndrome arising from trauma, sepsis, pneumonia, aspiration, burns and other pulmonary diseases. |
format | Online Article Text |
id | pubmed-7124456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71244562020-04-08 Systemic oxygen delivery by peritoneal perfusion of oxygen microbubbles Feshitan, Jameel A. Legband, Nathan D. Borden, Mark A. Terry, Benjamin S. Biomaterials Article Severe hypoxemia refractory to pulmonary mechanical ventilation remains life-threatening in critically ill patients. Peritoneal ventilation has long been desired for extrapulmonary oxygenation owing to easy access of the peritoneal cavity for catheterization and the relative safety compared to an extracorporeal circuit. Unfortunately, prior attempts involving direct oxygen ventilation or aqueous perfusates of fluorocarbons or hemoglobin carriers have failed, leading many researchers to abandon the method. We attribute these prior failures to limited mass transfer of oxygen to the peritoneum and have designed an oxygen formulation that overcomes this limitation. Using phospholipid-coated oxygen microbubbles (OMBs), we demonstrate 100% survival for rats experiencing acute lung trauma to at least 2 h. In contrast, all untreated rats and rats treated with peritoneal oxygenated saline died within 30 min. For rats treated with OMBs, hemoglobin saturation and heart rate were at normal levels over the 2-h timeframe. Peritoneal oxygenation with OMBs was therefore shown to be safe and effective, and the method requires less equipment and technical expertise than initiating and maintaining an extracorporeal circuit. Further translation of peritoneal oxygenation with OMBs may provide therapy for acute respiratory distress syndrome arising from trauma, sepsis, pneumonia, aspiration, burns and other pulmonary diseases. Elsevier Ltd. 2014-03 2014-01-15 /pmc/articles/PMC7124456/ /pubmed/24439406 http://dx.doi.org/10.1016/j.biomaterials.2013.12.070 Text en Copyright © 2013 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Feshitan, Jameel A. Legband, Nathan D. Borden, Mark A. Terry, Benjamin S. Systemic oxygen delivery by peritoneal perfusion of oxygen microbubbles |
title | Systemic oxygen delivery by peritoneal perfusion of oxygen microbubbles |
title_full | Systemic oxygen delivery by peritoneal perfusion of oxygen microbubbles |
title_fullStr | Systemic oxygen delivery by peritoneal perfusion of oxygen microbubbles |
title_full_unstemmed | Systemic oxygen delivery by peritoneal perfusion of oxygen microbubbles |
title_short | Systemic oxygen delivery by peritoneal perfusion of oxygen microbubbles |
title_sort | systemic oxygen delivery by peritoneal perfusion of oxygen microbubbles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7124456/ https://www.ncbi.nlm.nih.gov/pubmed/24439406 http://dx.doi.org/10.1016/j.biomaterials.2013.12.070 |
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