Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/26625
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dc.contributor.authorMiles, Lachlan F-
dc.contributor.authorMakar, Timothy-
dc.contributor.authorOughton, Chad W-
dc.contributor.authorPeyton, Philip J-
dc.date2021-05-26-
dc.date.accessioned2021-05-31T22:59:09Z-
dc.date.available2021-05-31T22:59:09Z-
dc.date.issued2021-05-
dc.identifier.citationAnaesthesia and Intensive Care 2021; 49(3): 206-213en
dc.identifier.issn0310-057X-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/26625-
dc.description.abstractPowered air-purifying respirators (PAPR) are a high level of respiratory personal protective equipment. Like all mechanical devices, they are vulnerable to failure. The precise physiological consequences of failure in live subjects have not previously been reported. We conducted an observational safety study simulating PAPR failure in a group of nine healthy volunteers, wearing loose-fitting hoods, who were observed for a period of ten minutes, or until they requested the experiment be aborted, with continuous monitoring of gas exchange. Relative to baseline, participants demonstrated median reductions in peripheral oxygen saturation of 3.5% (95% confidence interval (CI) -4% to -2%; P = 0.0039) and fraction of inspired oxygen of 0.045 (95% CI -0.05 to -0.04; P = 0.0039), and median increases in inspired partial pressure of carbon dioxide of 27 mmHg (95% CI 23.5-32 mmHg; P = 0.0039), end-tidal partial pressure of carbon dioxide of 11 mmHg (95% CI 7-16 mmHg; P = 0.0039) and minute ventilation of 30 l/min (95% CI 19.4-35.9 l/min; P = 0.0039). Median collateral entrainment of room air into the hood was 17.6 l/min (interquartile range 12.3-27.0 l/min). All subjects reported thermal discomfort, with two (22.2%) requesting early termination of the experiment. Whilst the degree of rebreathing in this experiment was not sufficient to cause dangerous physiological derangement, the degree of reported thermal discomfort combined with the consequences of entrainment of possibly contaminated air into the hood, pose a risk to wearers in the event of failure.en
dc.language.isoeng-
dc.subjectCOVID-19en
dc.subjecthealth personnelen
dc.subjectpersonal protective devicesen
dc.subjectpersonal protective equipment (PPE)en
dc.subjectrespiratory function: dead spaceen
dc.titleVentilatory parameters measured during a physiological study of simulated powered air-purifying respirator failure in healthy volunteers.en
dc.typeJournal Articleen
dc.identifier.journaltitleAnaesthesia and Intensive Careen
dc.identifier.affiliationAnaesthesiaen
dc.identifier.affiliationCentre for Integrated Critical Care, The University of Melbourne, Melbourne, Australiaen
dc.identifier.doi10.1177/0310057X20978982en
dc.type.contentTexten
dc.identifier.orcid0000-0003-2044-5560en
dc.identifier.orcid0000-0003-1185-2869en
dc.identifier.pubmedid34039044-
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