Covid-19 antigen testing: better than we know? A test accuracy study
- PMID: 33985403
- PMCID: PMC8127166
- DOI: 10.1080/23744235.2021.1914857
Covid-19 antigen testing: better than we know? A test accuracy study
Abstract
Background: Antigen testing for SARS-CoV-2 is considered to be less sensitive than the standard reference method - real-time PCR (RT-PCR). It has been suggested that many patients with positive RT-PCR 'missed' by antigen testing might be non-infectious.
Methods: In a real-world high-throughput setting for asymptomatic or mildly symptomatic patients, 494 patients were tested using RT-PCR as well as a single lateral flow antigen test (Ecotest, AssureTech, China). Where the results differed, virus viability was evaluated by cell culture. The test parameters were calculated with RT-PCR and RT-PCR adjusted on viability as reference standards.
Results: The overall sensitivity of the used antigen test related to the RT-PCR only was 76.2%, specificity was 97.3%. However, 36 out of 39 patients 'missed' by the antigen test contained no viable virus. After adjusting on that, the sensitivity grew to 97.7% and, more importantly for disease control purposes, the negative predictive value reached 99.2%.
Conclusions: We propose that viability testing should be always performed when evaluating a new antigen test. A well-chosen and validated antigen test provides excellent results in identifying patients who are shedding viable virus (although some caveats still remain) in the real-world high-throughput setting of asymptomatic or mildly symptomatic individuals.
Keywords: Covid-19; SARS-CoV-2; antigen testing; sensitivity; virus shedding; virus viability.
Conflict of interest statement
All Authors declare that they have no conflict of interest regarding the research presented in this paper
References
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- ECDC (European Centre for Disease Control). Options for the use of rapid antigen tests for COVID-19 in the EU/EEA and the UK: ECDC, 2020. [cited 2020 Dec 30]. Available from: https://www.ecdc.europa.eu/en/publications-data/options-use-rapid-antige...
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- European Commission . Commission recommendation of 28.10.2020 on COVID-19 testing strategies, including the use of rapid antigen tests. Brussels (Belgium): European Commission; 2020.
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- World Health Organization. Antigen-detection in the diagnosis of SARS-CoV-2 infection using rapid immunoassays: interim guidance, 11 September 2020. Geneva (Switzerland): World Health Organization, 2020. 4
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