Surface and Air Contamination With Severe Acute Respiratory Syndrome Coronavirus 2 From Hospitalized Coronavirus Disease 2019 Patients in Toronto, Canada, March–May 2020
Author(s) -
Jonathon D. Kotwa,
Alainna Jamal,
Hamza Mbareche,
Lily Yip,
Patryk Aftanas,
Shiva Barati,
Natalie G. Bell,
Elizabeth Bryce,
Eric A. Coomes,
Gloria Crowl,
Caroline Duchaine,
Amna Faheem,
Lubna Farooqi,
Ryan Hiebert,
Kevin Katz,
Saman Khan,
Robert Kozak,
Angel X. Li,
Henna Mistry,
Mohammad Mozafarihashjin,
Jalees A. Nasir,
Kuganya Nirmalarajah,
Emily M. Panousis,
Aimee Paterson,
Simon Plenderleith,
Jeff Powis,
Karren Prost,
Renée Schryer,
Maureen Taylor,
Marc Veillette,
Titus Wong,
Xi Zhong,
Andrew G McArthur,
Allison J McGeer,
Samira Mubareka
Publication year - 2021
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1093/infdis/jiab578
Subject(s) - medicine , coronavirus , respiratory system , virus , covid-19 , contamination , virology , respiratory disease , emergency medicine , disease , infectious disease (medical specialty) , biology , lung , ecology
Background We determined the burden of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in air and on surfaces in rooms of patients hospitalized with coronavirus disease 2019 (COVID-19) and investigated patient characteristics associated with SARS-CoV-2 environmental contamination. Methods Nasopharyngeal swabs, surface, and air samples were collected from the rooms of 78 inpatients with COVID-19 at 6 acute care hospitals in Toronto from March to May 2020. Samples were tested for SARS-CoV-2 ribonucleic acid (RNA), cultured to determine potential infectivity, and whole viral genomes were sequenced. Association between patient factors and detection of SARS-CoV-2 RNA in surface samples were investigated. Results Severe acute respiratory syndrome coronavirus 2 RNA was detected from surfaces (125 of 474 samples; 42 of 78 patients) and air (3 of 146 samples; 3 of 45 patients); 17% (6 of 36) of surface samples from 3 patients yielded viable virus. Viral sequences from nasopharyngeal and surface samples clustered by patient. Multivariable analysis indicated hypoxia at admission, polymerase chain reaction-positive nasopharyngeal swab (cycle threshold of ≤30) on or after surface sampling date, higher Charlson comorbidity score, and shorter time from onset of illness to sampling date were significantly associated with detection of SARS-CoV-2 RNA in surface samples. Conclusions The infrequent recovery of infectious SARS-CoV-2 virus from the environment suggests that the risk to healthcare workers from air and near-patient surfaces in acute care hospital wards is likely limited.
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