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JAMA Netw Open . Assessment of Air Contamination by SARS-CoV-2 in Hospital Settings

tetano

Editor, Senior Moderator
JAMA Netw Open


. 2020 Dec 1;3(12):e2033232.
doi: 10.1001/jamanetworkopen.2020.33232.
Assessment of Air Contamination by SARS-CoV-2 in Hospital Settings


Gabriel Birgand[SUP] 1 2 [/SUP], Nathan Peiffer-Smadja[SUP] 1 3 4 5 6 [/SUP], Sandra Fournier[SUP] 7 [/SUP], Solen Kerneis[SUP] 8 9 [/SUP], Fran?ois-Xavier Lescure[SUP] 3 4 5 6 [/SUP], Jean-Christophe Lucet[SUP] 3 5 10 [/SUP]



Affiliations

Abstract

Importance: Controversy remains regarding the transmission routes of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
Objective: To review current evidence on air contamination with SARS-CoV-2 in hospital settings and the factors associated with contamination, including viral load and particle size.
Evidence review: The MEDLINE, Embase, and Web of Science databases were systematically queried for original English-language articles detailing SARS-CoV-2 air contamination in hospital settings between January 1 and October 27, 2020. This study was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR) guidelines. The positivity rate of SARS-CoV-2 viral RNA and culture were described and compared according to the setting, clinical context, air ventilation system, and distance from patients. The SARS-CoV-2 RNA concentrations in copies per meter cubed of air were pooled, and their distribution was described by hospital areas. Particle sizes and SARS-CoV-2 RNA concentrations in copies or median tissue culture infectious dose (TCID50) per meter cubed were analyzed after categorization as less than 1 μm, from 1 to 4 μm, and greater than 4 μm.
Findings: Among 2284 records identified, 24 cross-sectional observational studies were included in the review. Overall, 82 of 471 air samples (17.4%) from close patient environments were positive for SARS-CoV-2 RNA, with a significantly higher positivity rate in intensive care unit settings (intensive care unit, 27 of 107 [25.2%] vs non-intensive care unit, 39 of 364 [10.7%]; P < .001). There was no difference according to the distance from patients (≤1 m, 3 of 118 [2.5%] vs >1-5 m, 13 of 236 [5.5%]; P = .22). The positivity rate was 5 of 21 air samples (23.8%) in toilets, 20 of 242 (8.3%) in clinical areas, 15 of 122 (12.3%) in staff areas, and 14 of 42 (33.3%) in public areas. A total of 81 viral cultures were performed across 5 studies, and 7 (8.6%) from 2 studies were positive, all from close patient environments. The median (interquartile range) SARS-CoV-2 RNA concentrations varied from 1.0 ? 103 copies/m3 (0.4 ? 103 to 3.1 ? 103 copies/m3) in clinical areas to 9.7 ? 103 copies/m3 (5.1 ? 103 to 14.3 ? 103 copies/m3) in the air of toilets or bathrooms. Protective equipment removal and patient rooms had high concentrations per titer of SARS-CoV-2 (varying from 0.9 ? 103 to 40 ? 103 copies/m3 and 3.8 ? 103 to 7.2 ? 103 TCID50/m3), with aerosol size distributions that showed peaks in the region of particle size less than 1 μm; staff offices had peaks in the region of particle size greater than 4 μm.
Conclusions and relevance: In this systematic review, the air close to and distant from patients with coronavirus disease 2019 was frequently contaminated with SARS-CoV-2 RNA; however, few of these samples contained viable viruses. High viral loads found in toilets and bathrooms, staff areas, and public hallways suggest that these areas should be carefully considered.
 
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