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Diagnostic accuracy of rapid antigen tests in asymptomatic and presymptomatic close contacts of individuals with confirmed SARS-CoV-2 infection

Title: Diagnostic accuracy of rapid antigen tests in asymptomatic and presymptomatic close contacts of individuals with confirmed SARS-CoV-2 infection
Authors: E (Ewoud) Schuit; IK (Irene) Veldhuijzen; Roderick P. Venekamp; Wouter Bijllaardt; SD (Suzan) Diepstraten - Pas; Esther B. Lodder; R. (Richard) Molenkamp; C.H. (Corine) Geurts van Kessel; J (Jans) Velzing; Robin C. Huisman; Lieke Brouwer; Timo L. Boelsums; Gregorius J. Sips; Kimberly S.M. Benschop; Lotty Hooft; Janneke H.H.M. Van De Wijgert; S. van t Hof; Karel G.M. Moons
Source: The BMJ vol. 374
Publication Year: 2021
Collection: RePub - Publications from Erasmus University, Rotterdam
Description: Objective To assess the diagnostic test accuracy of two rapid antigen tests in asymptomatic and presymptomatic close contacts of people with SARS-CoV-2 infection on day 5 after exposure. Design Prospective cross sectional study. Setting Four public health service covid-19 test sites in the Netherlands. Participants 4274 consecutively included close contacts (identified through test-and-trace programme or contact tracing app) aged 16 years or older and asymptomatic for covid-19 when requesting a test. Main outcome measures Sensitivity, specificity, and positive and negative predictive values of Veritor System (Beckton Dickinson) and Biosensor (Roche Diagnostics) rapid antigen tests, with reverse-transcriptase polymerase chain reaction (RT-PCR) testing as reference standard. The viral load cut-off above which 95% of people with a positive RT-PCR test result were virus culture positive was used as a proxy of infectiousness. Results Of 2678 participants tested with Veritor, 233 (8.7%) had a RT-PCR confirmed SARS-CoV-2 infection of whom 149 were also detected by the rapid antigen test (sensitivity 63.9%, 95% confidence interval 57.4% to 70.1%). Of 1596 participants tested with Biosensor, 132 (8.3%) had a RT-PCR confirmed SARS-CoV-2 infection of whom 83 were detected by the rapid antigen test (sensitivity 62.9%, 54.0% to 71.1%). In those who were still asymptomatic at the time of sampling, sensitivity was 58.7% (51.1% to 66.0%) for Veritor (n=2317) and 59.4% (49.2% to 69.1%) for Biosensor (n=1414), and in those who developed symptoms were 84.2% (68.7% to 94.0%; n=219) for Veritor and 73.3% (54.1% to 87.7%; n=158) for Biosensor. When a viral load cut-off was applied for infectiouness (≥5.2 log10 SARS-CoV-2 E gene copies/mL), the overall sensitivity was 90.1% (84.2% to 94.4%) for Veritor and 86.8% (78.1% to 93.0%) for Biosensor, and 88.1% (80.5% to 93.5%) for Veritor and 85.1% (74.3% to 92.6%) for Biosensor, among those who remained asymptomatic throughout. Specificities were >99%, and positive and negative ...
Document Type: article in journal/newspaper
Language: unknown
Relation: https://repub.eur.nl/pub/135773; urn:hdl:1765/135773
DOI: 10.1136/bmj.n1676
Availability: https://repub.eur.nl/pub/135773; https://doi.org/10.1136/bmj.n1676
Accession Number: edsbas.FB12F01F
Database: BASE