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Particulate generation with different oxygen delivery devices

BACKGROUND: The Coronavirus pandemic has a high mortality rate in patients that are mechanically ventilated, which has led to an ever increasing interest in noninvasive forms of oxygenation. The use of these devices has the theoretical risk of increased exposure risk because of possible particulate...

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Autores principales: Helgeson, Scott A., Lee, Augustine S., Lim, Kaiser G., Niven, Alexander S., Patel, Neal M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016732/
https://www.ncbi.nlm.nih.gov/pubmed/33836331
http://dx.doi.org/10.1016/j.rmed.2021.106386
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author Helgeson, Scott A.
Lee, Augustine S.
Lim, Kaiser G.
Niven, Alexander S.
Patel, Neal M.
author_facet Helgeson, Scott A.
Lee, Augustine S.
Lim, Kaiser G.
Niven, Alexander S.
Patel, Neal M.
author_sort Helgeson, Scott A.
collection PubMed
description BACKGROUND: The Coronavirus pandemic has a high mortality rate in patients that are mechanically ventilated, which has led to an ever increasing interest in noninvasive forms of oxygenation. The use of these devices has the theoretical risk of increased exposure risk because of possible particulate generation. This study aimed to quantify the particulate generation associated with different oxygen devices. METHODS: This was a prospective single center study conducted during September 2020 using ten healthy adult volunteers. Testing was conducted in a negative pressure hospital room using a light scattering particle counter. The oxygen devices used were a nasal cannula, an OxyMask™, a non-rebreathing mask, and a high flow system. Particle measurements were obtained at baseline in the room and then with each oxygen delivery device and pre-specified oxygen flow rates. These measurements were obtained different distances from the volunteer with their mouth open. A Wilcoxon/Kruskal-Wallis test was performed on each separate oxygen modality with all flow rates as one model. RESULTS: The particle concentrations were slightly non-significantly increased with the OxyMask™ and non-rebreathing mask at the closest distance measured. As the distance increased, these counts decreased closer to ambient levels. The nasal cannula and high flow nasal cannula particle counts were not significantly different from ambient measurements at either distance. CONCLUSION: Nasal cannula, OxyMask™, non-rebreathing mask, and high flow oxygen did not generate any additional aerosols or droplets above a baseline room measurement, but further studies are necessary to determine infectious risk.
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spelling pubmed-80167322021-04-02 Particulate generation with different oxygen delivery devices Helgeson, Scott A. Lee, Augustine S. Lim, Kaiser G. Niven, Alexander S. Patel, Neal M. Respir Med Short Communication BACKGROUND: The Coronavirus pandemic has a high mortality rate in patients that are mechanically ventilated, which has led to an ever increasing interest in noninvasive forms of oxygenation. The use of these devices has the theoretical risk of increased exposure risk because of possible particulate generation. This study aimed to quantify the particulate generation associated with different oxygen devices. METHODS: This was a prospective single center study conducted during September 2020 using ten healthy adult volunteers. Testing was conducted in a negative pressure hospital room using a light scattering particle counter. The oxygen devices used were a nasal cannula, an OxyMask™, a non-rebreathing mask, and a high flow system. Particle measurements were obtained at baseline in the room and then with each oxygen delivery device and pre-specified oxygen flow rates. These measurements were obtained different distances from the volunteer with their mouth open. A Wilcoxon/Kruskal-Wallis test was performed on each separate oxygen modality with all flow rates as one model. RESULTS: The particle concentrations were slightly non-significantly increased with the OxyMask™ and non-rebreathing mask at the closest distance measured. As the distance increased, these counts decreased closer to ambient levels. The nasal cannula and high flow nasal cannula particle counts were not significantly different from ambient measurements at either distance. CONCLUSION: Nasal cannula, OxyMask™, non-rebreathing mask, and high flow oxygen did not generate any additional aerosols or droplets above a baseline room measurement, but further studies are necessary to determine infectious risk. Elsevier Ltd. 2021-05 2021-04-02 /pmc/articles/PMC8016732/ /pubmed/33836331 http://dx.doi.org/10.1016/j.rmed.2021.106386 Text en © 2021 Elsevier Ltd. 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 Short Communication
Helgeson, Scott A.
Lee, Augustine S.
Lim, Kaiser G.
Niven, Alexander S.
Patel, Neal M.
Particulate generation with different oxygen delivery devices
title Particulate generation with different oxygen delivery devices
title_full Particulate generation with different oxygen delivery devices
title_fullStr Particulate generation with different oxygen delivery devices
title_full_unstemmed Particulate generation with different oxygen delivery devices
title_short Particulate generation with different oxygen delivery devices
title_sort particulate generation with different oxygen delivery devices
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016732/
https://www.ncbi.nlm.nih.gov/pubmed/33836331
http://dx.doi.org/10.1016/j.rmed.2021.106386
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