Quantification of aerosol dispersal from suspected aerosol-generating procedures.


Journal

ERJ open research
ISSN: 2312-0541
Titre abrégé: ERJ Open Res
Pays: England
ID NLM: 101671641

Informations de publication

Date de publication:
Oct 2021
Historique:
received: 22 03 2021
accepted: 11 09 2021
entrez: 8 12 2021
pubmed: 9 12 2021
medline: 9 12 2021
Statut: epublish

Résumé

Oxygen-delivering modalities like humidified high-flow nasal cannula (HFNC) and noninvasive positive-pressure ventilation (NIV) are suspected of generating aerosols that may contribute to transmission of disease such as coronavirus disease 2019. We sought to assess if these modalities lead to increased aerosol dispersal compared to the use of non-humidified low-flow nasal cannula oxygen treatment (LFNC). Aerosol dispersal from 20 healthy volunteers using HFNC, LFNC and NIV oxygen treatment was measured in a controlled chamber. We investigated effects related to coughing and using a surgical face mask in combination with the oxygen delivering modalities. An aerodynamic particle sizer measured aerosol particles (APS3321, 0.3-20 µm) directly in front of the subjects, while a mesh of smaller particle sensors (SPS30, 0.3-10 µm) was distributed in the test chamber. Non-productive coughing led to significant increases in particle dispersal close to the face when using LFNC and HFNC but not when using NIV. HFNC or NIV did not lead to a statistically significant increase in aerosol dispersal compared to LFNC. With non-productive cough in a room without air changes, there was a significant drop in particle levels between 100 cm and 180 cm from the subjects. Our results indicate that using HFNC and NIV does not lead to increased aerosol dispersal compared to low-flow oxygen treatment, except in rare cases. For a subject with non-productive cough, NIV with double-limb circuit and non-vented mask may be a favourable choice to reduce the risk for aerosol spread.

Sections du résumé

BACKGROUND BACKGROUND
Oxygen-delivering modalities like humidified high-flow nasal cannula (HFNC) and noninvasive positive-pressure ventilation (NIV) are suspected of generating aerosols that may contribute to transmission of disease such as coronavirus disease 2019. We sought to assess if these modalities lead to increased aerosol dispersal compared to the use of non-humidified low-flow nasal cannula oxygen treatment (LFNC).
METHODS METHODS
Aerosol dispersal from 20 healthy volunteers using HFNC, LFNC and NIV oxygen treatment was measured in a controlled chamber. We investigated effects related to coughing and using a surgical face mask in combination with the oxygen delivering modalities. An aerodynamic particle sizer measured aerosol particles (APS3321, 0.3-20 µm) directly in front of the subjects, while a mesh of smaller particle sensors (SPS30, 0.3-10 µm) was distributed in the test chamber.
RESULTS RESULTS
Non-productive coughing led to significant increases in particle dispersal close to the face when using LFNC and HFNC but not when using NIV. HFNC or NIV did not lead to a statistically significant increase in aerosol dispersal compared to LFNC. With non-productive cough in a room without air changes, there was a significant drop in particle levels between 100 cm and 180 cm from the subjects.
CONCLUSIONS CONCLUSIONS
Our results indicate that using HFNC and NIV does not lead to increased aerosol dispersal compared to low-flow oxygen treatment, except in rare cases. For a subject with non-productive cough, NIV with double-limb circuit and non-vented mask may be a favourable choice to reduce the risk for aerosol spread.

Identifiants

pubmed: 34877350
doi: 10.1183/23120541.00206-2021
pii: 00206-2021
pmc: PMC8474485
pii:
doi:

Types de publication

Journal Article

Langues

eng

Informations de copyright

Copyright ©The authors 2021.

Déclaration de conflit d'intérêts

Conflict of interest: R. Strand-Amundsen has nothing to disclose. Conflict of interest: C. Tronstad has nothing to disclose. Conflict of interest: O. Elvebakk has nothing to disclose. Conflict of interest: T. Martinsen has nothing to disclose. Conflict of interest: M. Dybwad has nothing to disclose. Conflict of interest: E. Lingaas has nothing to disclose. Conflict of interest: T.I. Tønnessen has nothing to disclose.

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Auteurs

Runar Strand-Amundsen (R)

Dept of Clinical and Biomedical Engineering, Oslo University Hospital, Oslo, Norway.

Christian Tronstad (C)

Dept of Clinical and Biomedical Engineering, Oslo University Hospital, Oslo, Norway.

Ole Elvebakk (O)

Dept of Clinical and Biomedical Engineering, Oslo University Hospital, Oslo, Norway.

Tormod Martinsen (T)

Dept of Clinical and Biomedical Engineering, Oslo University Hospital, Oslo, Norway.

Marius Dybwad (M)

Norwegian Defence Research Establishment (FFI), Kjeller, Norway.

Egil Lingaas (E)

Dept of Infection Prevention, Oslo University Hospital - Rikshospitalet, Oslo, Norway.

Tor Inge Tønnessen (TI)

Dept of Anaesthesiology, Division of Emergencies and Critical Care, Oslo University Hospital, Oslo, Norway.
Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.

Classifications MeSH