Viable SARS-CoV-2 detected in the air of hospital rooms of patients with COVID-19 with an early infection
•Viable SARS-CoV-2 can be detected in the air around patients with an early infection.•Airborne viable SARS-CoV-2 is associated with high levels of airborne viral RNA.•Airborne SARS-CoV-2 is not related to nasopharyngeal viral RNA and viable virus. This study assessed the concentration of SARS-CoV-2...
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Veröffentlicht in: | International journal of infectious diseases 2023-01, Vol.126, p.73-78 |
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Sprache: | eng |
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Zusammenfassung: | •Viable SARS-CoV-2 can be detected in the air around patients with an early infection.•Airborne viable SARS-CoV-2 is associated with high levels of airborne viral RNA.•Airborne SARS-CoV-2 is not related to nasopharyngeal viral RNA and viable virus.
This study assessed the concentration of SARS-CoV-2 in the air of hospital rooms occupied by patients with COVID-19 who had viable SARS-CoV-2 in nasopharyngeal (NP) samples in early infection.
Between July and October 2021, NP swabs were collected from 20 patients with early SARS-CoV-2 infection admitted to a tertiary hospital in Japan. Air samples were collected from their rooms, tested for SARS-CoV-2 RNA, and cultured to determine potential infectivity.
The NP swab samples of 18 patients were positive for viable SARS-CoV-2 (median concentration: 4.0 × 105 tissue culture infectious dose 50/ml). In the air samples, viral RNA (median concentration: 1.1 × 105 copies/m3) was detected in 12/18 (67%) patients, and viable virus (median concentration: 8.9 × 102 tissue culture infectious dose 50/m3) was detected in 5/18 (28%) patients. The median time between illness onset and sampling was 3 days. The RNA concentration was significantly higher in samples wherein viable SARS-CoV-2 was detected than in samples in which viable virus was not detected (P-value = 0.027).
Viable SARS-CoV-2 can be detected in the air surrounding patients with early SARS-CoV-2 infection. Health care workers should pay attention to infection control when caring for patients with early SARS-CoV-2 infection. |
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ISSN: | 1201-9712 1878-3511 |
DOI: | 10.1016/j.ijid.2022.11.003 |