2021
DOI: 10.1016/j.jinf.2021.07.038
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Real-world evaluation of COVID-19 lateral flow device (LFD) mass-testing in healthcare workers at a London hospital; a prospective cohort analysis

Abstract: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article. Please note that, during the production process, errors may be discovered which could affect the content, a… Show more

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Cited by 16 publications
(28 citation statements)
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“…Most of the datasets were from the United Kingdom (8; 47.1% of all data sets) [15,16,28,29,33,34], and the others from Germany (4; 23.5% of all data sets) [17,27,32], Austria (3; 17.6% of all data sets) [31], and the Netherlands (2; 11.8% of all data sets) [30]. In eight data sets (47.1% of all data sets) [15,16,28,29,33,34], the Innova SARS-CoV-2 Rapid Antigen Self-Test Kit (Innova Medical Group Inc., United States [CA]; henceforth called ‘Innova’) was used. The STANDARD Q COVID-19 Ag Home Test (SD Biosensor, South Korea; distributed in Europe by Roche, Germany; henceforth called ‘Standard Q’) [30,35] and the SARS-CoV-2 Antigen Rapid Test Kit (Lepu Medical Technology, China) [31] were used in three data sets each (17.6% of all data sets).…”
Section: Resultsmentioning
confidence: 99%
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“…Most of the datasets were from the United Kingdom (8; 47.1% of all data sets) [15,16,28,29,33,34], and the others from Germany (4; 23.5% of all data sets) [17,27,32], Austria (3; 17.6% of all data sets) [31], and the Netherlands (2; 11.8% of all data sets) [30]. In eight data sets (47.1% of all data sets) [15,16,28,29,33,34], the Innova SARS-CoV-2 Rapid Antigen Self-Test Kit (Innova Medical Group Inc., United States [CA]; henceforth called ‘Innova’) was used. The STANDARD Q COVID-19 Ag Home Test (SD Biosensor, South Korea; distributed in Europe by Roche, Germany; henceforth called ‘Standard Q’) [30,35] and the SARS-CoV-2 Antigen Rapid Test Kit (Lepu Medical Technology, China) [31] were used in three data sets each (17.6% of all data sets).…”
Section: Resultsmentioning
confidence: 99%
“…In 14 datasets (77.8% of all datasets) [15-17,27-29,31-34], C19ST was implemented as part of a routinely testing service, most often (4 datasets) [29,31,33,34] for testing twice weekly. C19ST was mainly performed at home (10 data sets; 58.8%), but also in school (4; 23.5% of all data sets) [27,31] or at work (1; 5.9% of all data sets) [34].…”
Section: Resultsmentioning
confidence: 99%
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“…There was an urgent need to review the testing programme in Professional Rugby to agree the most cost-effective and accurate testing modality. We read with interest the real-world evaluation of antigen-based rapid diagnostic tests (Ag-RDTs) for COVID-19 and the high uptake for mass testing amongst healthcare workers [5] . To provide oversight, advice, and guidance on the scope of testing for SARS-CoV-2 by Ag-RDT, Premiership Rugby and Rugby Football Union approved this rapid collaborative service evaluation.…”
mentioning
confidence: 99%