» Articles » PMID: 34230058

Performance of the Innova SARS-CoV-2 Antigen Rapid Lateral Flow Test in the Liverpool Asymptomatic Testing Pilot: Population Based Cohort Study

Overview
Journal BMJ
Specialty General Medicine
Date 2021 Jul 7
PMID 34230058
Citations 49
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: To assess the performance of the SARS-CoV-2 antigen rapid lateral flow test (LFT) versus polymerase chain reaction testing in the asymptomatic general population attending testing centres.

Design: Observational cohort study.

Setting: Community LFT pilot at covid-19 testing sites in Liverpool, UK.

Participants: 5869 asymptomatic adults (≥18 years) voluntarily attending one of 48 testing sites during 6-29 November 2020.

Interventions: Participants were tested using both an Innova LFT and a quantitative reverse-transcriptase polymerase chain reaction (RT-qPCR) test based on supervised self-administered swabbing at testing sites.

Main Outcome Measures: Sensitivity, specificity, and predictive values of LFT compared with RT-qPCR in an epidemic steady state of covid-19 among adults with no classic symptoms of the disease.

Results: Of 5869 test results, 22 (0.4%) LFT results and 343 (5.8%) RT-qPCR results were void (that is, when the control line fails to appear within 30 minutes). Excluding the void results, the LFT versus RT-qPCR showed a sensitivity of 40.0% (95% confidence interval 28.5% to 52.4%; 28/70), specificity of 99.9% (99.8% to 99.99%; 5431/5434), positive predictive value of 90.3% (74.2% to 98.0%; 28/31), and negative predictive value of 99.2% (99.0% to 99.4%; 5431/5473). When the void samples were assumed to be negative, a sensitivity was observed for LFT of 37.8% (26.8% to 49.9%; 28/74), specificity of 99.6% (99.4% to 99.8%; 5431/5452), positive predictive value of 84.8% (68.1% to 94.9%; 28/33), and negative predictive value of 93.4% (92.7% to 94.0%; 5431/5814). The sensitivity in participants with an RT-qPCR cycle threshold (Ct) of <18.3 (approximate viral loads >10 RNA copies/mL) was 90.9% (58.7% to 99.8%; 10/11), a Ct of <24.4 (>10 RNA copies/mL) was 69.4% (51.9% to 83.7%; 25/36), and a Ct of >24.4 (<10 RNA copies/mL) was 9.7% (1.9% to 23.7%; 3/34). LFT is likely to detect at least three fifths and at most 998 in every 1000 people with a positive RT-qPCR test result with high viral load.

Conclusions: The Innova LFT can be useful for identifying infections among adults who report no symptoms of covid-19, particularly those with high viral load who are more likely to infect others. The number of asymptomatic adults with lower Ct (indicating higher viral load) missed by LFT, although small, should be considered when using single LFT in high consequence settings. Clear and accurate communication with the public about how to interpret test results is important, given the chance of missing some cases, even at high viral loads. Further research is needed to understand how infectiousness is reflected in the viral antigen shedding detected by LFT versus the viral loads approximated by RT-qPCR.

Citing Articles

How science and policy came together and made a global impact: The EU common list of COVID-19 antigen tests.

Raffael B, Petrillo M, Leoni G, Wiesenthal T, Kuipers Y, Querci M Open Res Eur. 2025; 4:198.

PMID: 39931571 PMC: 11809469. DOI: 10.12688/openreseurope.18267.2.


Effectiveness and user experience of nose and throat swabbing techniques for SARS-CoV-2 detection: results from the UK COVID-19 National Testing Programme.

Futschik M, Kulasegaran-Shylini R, Blandford E, Harper S, Chapman D, Turek E BMC Glob Public Health. 2025; 3(1):5.

PMID: 39806484 PMC: 11731392. DOI: 10.1186/s44263-024-00121-x.


Efficacy of rapid antigen self-testing for SARS-CoV-2 screening: Real-world evidence from a prospective cohort study.

Hu Y, Peng B, Fan J, Yang Z, Xue J, Long Q Genes Dis. 2024; 11(5):101151.

PMID: 38882010 PMC: 11176647. DOI: 10.1016/j.gendis.2023.101151.


Faster detection of asymptomatic COVID-19 cases among care home staff in England through the combination of SARS-CoV-2 testing technologies.

Ryan F, Cole-Hamilton J, Dandamudi N, Futschik M, Needham A, Saquib R Sci Rep. 2024; 14(1):7475.

PMID: 38553484 PMC: 10980794. DOI: 10.1038/s41598-024-57817-1.


Potential Application of SARS-CoV-2 Rapid Antigen Diagnostic Tests for the Detection of Infectious Individuals Attending Mass Gatherings - A Simulation Study.

McAloon C, Dahly D, Walsh C, Wall P, Smyth B, More S Front Epidemiol. 2024; 2:862826.

PMID: 38455312 PMC: 10911017. DOI: 10.3389/fepid.2022.862826.


References
1.
Dinnes J, Deeks J, Berhane S, Taylor M, Adriano A, Davenport C . Rapid, point-of-care antigen and molecular-based tests for diagnosis of SARS-CoV-2 infection. Cochrane Database Syst Rev. 2021; 3:CD013705. PMC: 8078597. DOI: 10.1002/14651858.CD013705.pub2. View

2.
Peto T . COVID-19: Rapid antigen detection for SARS-CoV-2 by lateral flow assay: A national systematic evaluation of sensitivity and specificity for mass-testing. EClinicalMedicine. 2021; 36:100924. PMC: 8164528. DOI: 10.1016/j.eclinm.2021.100924. View

3.
Armstrong S . Covid-19: Tests on students are highly inaccurate, early findings show. BMJ. 2020; 371:m4941. DOI: 10.1136/bmj.m4941. View

4.
Marks M, Millat-Martinez P, Ouchi D, Roberts C, Alemany A, Corbacho-Monne M . Transmission of COVID-19 in 282 clusters in Catalonia, Spain: a cohort study. Lancet Infect Dis. 2021; 21(5):629-636. PMC: 7906723. DOI: 10.1016/S1473-3099(20)30985-3. View

5.
Cevik M, Tate M, Lloyd O, Maraolo A, Schafers J, Ho A . SARS-CoV-2, SARS-CoV, and MERS-CoV viral load dynamics, duration of viral shedding, and infectiousness: a systematic review and meta-analysis. Lancet Microbe. 2021; 2(1):e13-e22. PMC: 7837230. DOI: 10.1016/S2666-5247(20)30172-5. View