Evidence map›Paper›PMID 33774019›Full record

ArticleThe Journal of infection2021

Exhaled SARS-CoV-2 quantified by face-mask sampling in hospitalised patients with COVID-19.

Caroline M Williams, Daniel Pan, Jonathan Decker, Anika Wisniewska, Eve Fletcher, Shirley Sze, Sara Assadi, Richard Haigh, Mohamad Abdulwhhab, Paul Bird and 7 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of infection, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
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  15. Exhaled SARS-CoV-2 RNA viral load kinetics measured by facemask sampling associates with household transmission.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2023
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  16. Observational
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 3 institutions in 2 countries.

Caroline M WilliamsDepartment of Respiratory Sciences, University of Leicester, United Kingdom; Department of Clinical Microbiology, University Hospitals of Leicester NHS Trust, United Kingdom; Department of Infectious Diseases and HIV Medicine, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom. Electronic address: cw329@le.ac.uk.
Daniel PanDepartment of Respiratory Sciences, University of Leicester, United Kingdom; Department of Infectious Diseases and HIV Medicine, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
Jonathan DeckerDepartment of Respiratory Sciences, University of Leicester, United Kingdom.
Anika WisniewskaDepartment of Respiratory Sciences, University of Leicester, United Kingdom.
Eve FletcherDepartment of Respiratory Sciences, University of Leicester, United Kingdom.
Shirley SzeDepartment of Cardiovascular Sciences, University of Leicester, United Kingdom.
Sara AssadiDepartment of Infectious Diseases and HIV Medicine, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
Richard HaighDepartment of Respiratory Sciences, University of Leicester, United Kingdom.
Mohamad AbdulwhhabDepartment of Respiratory Sciences, University of Leicester, United Kingdom.
Paul BirdDepartment of Respiratory Sciences, University of Leicester, United Kingdom; Department of Clinical Microbiology, University Hospitals of Leicester NHS Trust, United Kingdom.
Christopher W HolmesDepartment of Respiratory Sciences, University of Leicester, United Kingdom; Department of Clinical Microbiology, University Hospitals of Leicester NHS Trust, United Kingdom.
Alaa Al-TaieDepartment of Biomedical Engineering, Al-Nahrain University, Baghdad, Iraq.
Baber SaleemDepartment of Engineering, University of Leicester, United Kingdom.
Jingzhe PanDepartment of Engineering, University of Leicester, United Kingdom.
Natalie J GartonDepartment of Respiratory Sciences, University of Leicester, United Kingdom.
Manish PareekDepartment of Respiratory Sciences, University of Leicester, United Kingdom; Department of Infectious Diseases and HIV Medicine, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom. Electronic address: mp4246@le.ac.uk.
Michael R BarerDepartment of Respiratory Sciences, University of Leicester, United Kingdom; Department of Clinical Microbiology, University Hospitals of Leicester NHS Trust, United Kingdom. Electronic address: mrb19@le.ac.uk.
University of Leicester · GBUniversity Hospitals of Leicester NHS Trust · GBNahrain University · IQ

Funding

Medical Research Council MR/P023061/1Medical Research Council MR/S002278/1
6 · The paper itself

Abstract

backgroundHuman 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).

methodsBetween May and December 2020, we took two concomitant FMS and nasopharyngeal samples (NPS) over two days, starting within 24 h 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 min, 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: 1000-99,999 copies and High ≥ 100,000 copies per strip for FMS or per 100 µl for NPS.

results102 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 (<10-3.3 x 10

conclusionWe demonstrate a simple and effective method for detecting and quantifying exhaled SARS-CoV-2 in hospitalised patients with COVID-19. Higher FMS viral loads were more likely to be associated with developing severe disease compared to NPS viral loads. Similar to NPS, FMS viral load was highest in early disease and in those with active respiratory symptoms, highlighting the potential role of FMS in understanding infectivity.

Indexed as

COVID-19SARS-CoV-2HumansMasksMiddle AgedRNA, ViralViral LoadRNA, Viral

Identifiers

PMID33774019
PMCPMC7989096
OpenAlexW3138246579

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.