Head-to-head comparison of the accuracy of saliva and nasal rapid antigen SARS-CoV-2 self-testing: cross-sectional study

Publication date

2022-10-24

Authors

Schuit, EwoudORCID 0000-0002-9548-3214ISNI 000000039432776X
Venekamp, RoderickORCID 0000-0002-1446-9614ISNI 0000000393819260
Veldhuijzen, Irene K.
van den Bijllaardt, Wouter
Pas, Suzan D.
Stohr, Joep J.J.M.
Lodder, Esther B.
Hellwich, Marloes
Molenkamp, Richard
Igloi, Zsofia

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Abstract

Background: The diagnostic accuracy of unsupervised self-testing with rapid antigen diagnostic tests (Ag-RDTs) is mostly unknown. We studied the diagnostic accuracy of a self-performed SARS-CoV-2 saliva and nasal Ag-RDT in the general population. Methods: This large cross-sectional study consecutively included unselected individuals aged ≥ 16 years presenting for SARS-CoV-2 testing at three public health service test sites. Participants underwent molecular test sampling and received two self-tests (the Hangzhou AllTest Biotech saliva self-test and the SD Biosensor nasal self-test by Roche Diagnostics) to perform themselves at home. Diagnostic accuracy of both self-tests was assessed with molecular testing as reference. Results: Out of 2819 participants, 6.5% had a positive molecular test. Overall sensitivities were 46.7% (39.3–54.2%) for the saliva Ag-RDT and 68.9% (61.6–75.6%) for the nasal Ag-RDT. With a viral load cut-off (≥ 5.2 log10 SARS-CoV-2 E-gene copies/mL) as a proxy of infectiousness, these sensitivities increased to 54.9% (46.4–63.3%) and 83.9% (76.9–89.5%), respectively. For the nasal Ag-RDT, sensitivities were 78.5% (71.1–84.8%) and 22.6% (9.6–41.1%) in those symptomatic and asymptomatic at the time of sampling, which increased to 90.4% (83.8–94.9%) and 38.9% (17.3–64.3%) after applying the viral load cut-off. In those with and without prior SARS-CoV-2 infection, sensitivities were 36.8% (16.3–61.6%) and 72.7% (65.1–79.4%). Specificities were > 99% and > 99%, positive predictive values > 70% and > 90%, and negative predictive values > 95% and > 95%, for the saliva and nasal Ag-RDT, respectively, in most analyses. Most participants considered the self-performing and result interpretation (very) easy for both self-tests. Conclusions: The Hangzhou AllTest Biotech saliva self Ag-RDT is not reliable for SARS-CoV-2 detection, overall, and in all studied subgroups. The SD Biosensor nasal self Ag-RDT had high sensitivity in individuals with symptoms and in those without prior SARS-CoV-2 infection but low sensitivity in asymptomatic individuals and those with a prior SARS-CoV-2 infection which warrants further investigation.

Keywords

Antigen test, COVID-19, Cross-sectional Study, Diagnostic test accuracy, Nasal test, Rapid antigen detection test, Saliva test, SARS-CoV-2, General Medicine, Journal Article

Citation

Schuit, E, Venekamp, R P, Veldhuijzen, I K, van den Bijllaardt, W, Pas, S D, Stohr, J J J M, Lodder, E B, Hellwich, M, Molenkamp, R, Igloi, Z, Wijers, C, Vroom, I H, Nagel-Imming, C R S, Han, W G H, Kluytmans, J A J W, van den Hof, S, van de Wijgert, J H H M & Moons, K G M 2022, 'Head-to-head comparison of the accuracy of saliva and nasal rapid antigen SARS-CoV-2 self-testing : cross-sectional study', BMC Medicine, vol. 20, 406. https://doi.org/10.1186/s12916-022-02603-x