Exhaled SARS-CoV-2 quantified by face-mask sampling in hospitalised patients with covid-19
Autor: | Natalie J. Garton, Caroline M. Williams, Paul W Bird, Manish Pareek, Anika Wisniewska, Richard D. Haigh, Baber Saleem, Mohamad Abdulwhhab, Daniel Pan, Jingzhe Pan, Eve Fletcher, Alaa Al-Taie, Christopher W Holmes, Sara Assadi, Jonathan Decker, Shirley Sze, Michael R. Barer |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Microbiology (medical) medicine.medical_specialty Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) 030106 microbiology medicine.disease_cause Asymptomatic Virus Article 03 medical and health sciences 0302 clinical medicine Internal medicine Medicine Humans Sampling (medicine) 030212 general & internal medicine Respiratory system Coronavirus Infectivity Transmission (medicine) business.industry SARS-CoV-2 Masks COVID-19 Middle Aged Viral Load Orders of magnitude (mass) Infectious Diseases Concomitant RNA Viral medicine.symptom business Viral load |
Zdroj: | The Journal of Infection |
ISSN: | 1532-2742 0163-4453 |
Popis: | Background Human to human transmission of SARS-CoV-2 is driven by the respiratory route but little is known about the pattern and quantity of virus output from exhaled breath. We have previously shown that face-mask sampling (FMS) can detect exhaled tubercle bacilli and have adapted its use to quantify exhaled SARS-CoV-2 RNA in patients admitted to hospital with Coronavirus Disease-2019 (COVID-19). Methods Between May and December 2020, we took two concomitant FMS and nasopharyngeal samples (NPS) over two days, starting within 24 hours of a routine virus positive NPS in patients hospitalised with COVID-19, at University Hospitals of Leicester NHS Trust, UK. Participants were asked to wear a modified duckbilled facemask for 30 minutes, followed by a nasopharyngeal swab. Demographic, clinical, and radiological data, as well as International Severe Acute Respiratory and emerging Infections Consortium (ISARIC) mortality and deterioration scores were obtained. Exposed masks were processed by removal, dissolution and analysis of sampling matrix strips fixed within the mask by RT-qPCR. Viral genome copy numbers were determined and results classified as Negative; Low: ≤999 copies; Medium: 1,000-99,999 copies and High ≥ 100,000 copies per strip for FMS or per 100µl for NPS. Results 102 FMS and NPS were collected from 66 routinely positive patients; median age: 61 (IQR 49 - 77), of which FMS was positive in 38% of individuals and concomitant NPS was positive in 50%. Positive FMS viral loads varied over five orders of magnitude ( Graphical abstract Image, graphical abstract |
Databáze: | OpenAIRE |
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