Salivary detection of COVID-19: clinical performance of oral sponge sampling for SARS-CoV-2 testing
- PMID: 34877351
- PMCID: PMC8474486
- DOI: 10.1183/23120541.00396-2021
Salivary detection of COVID-19: clinical performance of oral sponge sampling for SARS-CoV-2 testing
Abstract
Background: The current diagnostic standard for coronavirus disease 2019 (COVID-19) is reverse transcriptase-polymerase chain reaction (RT-PCR) testing with nasopharyngeal (NP) swabs. The invasiveness and need for trained personnel make the NP technique unsuited for repeated community-based mass screening. We developed a technique to collect saliva in a simple and easy way with the sponges that are usually used for tamponade of epistaxis. This study was carried out to validate the clinical performance of oral sponge (OS) sampling for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) testing.
Methods: Over a period of 22 weeks, we collected prospectively 409 paired NP and OS samples from consecutive subjects presenting to a public community-based free screening centre. Subjects were referred by their attending physician because of recent COVID-19 symptoms (n = 147) or by the contact tracing staff of the French public health insurance because they were considered as close contacts of a laboratory-confirmed COVID-19 case (n = 262).
Results: In symptomatic subjects, RT-PCR SARS-CoV-2 testing with OS showed a 96.5% (95% CI: 89.6-94.8) concordance with NP testing, and a 93.2% (95% CI: 89.1-97.3) sensitivity when using the IdyllaTM platform and a sensitivity of 76.3% (95% CI: 69.4-83.2) on the Synlab Barla laboratory platform. In close contacts the NP-OS concordance (93.8%, 95% CI: 90.9-96.7) and OS sensitivity (71.9%, 95% CI: 66.5-77.3) were slightly lower.
Conclusion: These results strongly suggest that OS testing is a straightforward, low-cost and high-throughput sampling method that can be used for frequent RT-PCR testing of COVID-19 patients and mass screening of populations.
Copyright ©The authors 2021.
Conflict of interest statement
Provenance: Submitted article, peer reviewed. Conflict of interest: J. Boutros has nothing to disclose. Conflict of interest: J. Benzaquen has nothing to disclose. Conflict of interest: C.H. Marquette has nothing to disclose. Conflict of interest: M. Ilié has nothing to disclose. Conflict of interest: M. Labaky has nothing to disclose. Conflict of interest: D. Benchetrit has nothing to disclose. Conflict of interest: T. Lavrut has nothing to disclose. Conflict of interest: S. Leroy has nothing to disclose. Conflict of interest: R. Chemla has nothing to disclose. Conflict of interest: M. Carles has nothing to disclose. Conflict of interest: V. Tanga has nothing to disclose. Conflict of interest: C. Maniel has nothing to disclose. Conflict of interest: O. Bordone has nothing to disclose. Conflict of interest: M. Allégra has nothing to disclose. Conflict of interest: V. Lespinet has nothing to disclose. Conflict of interest: J. Fayada has nothing to disclose. Conflict of interest: J. Griffonnet has nothing to disclose. Conflict of interest: V. Hofman has nothing to disclose. Conflict of interest: P. Hofman is a member of the scientific advisory board (group of European experts) of Biocartis; however, this board is totally independent of Biocartis.
Figures
References
-
- Sullivan PS, Sailey C, Guest JL, et al. . Detection of SARS-CoV-2 RNA and antibodies in diverse samples: protocol to validate the sufficiency of provider-observed, home-collected blood, saliva, and oropharyngeal samples. JMIR Public Health Surveill 2020; 6: e19054. doi:10.2196/19054 - DOI - PMC - PubMed
LinkOut - more resources
Full Text Sources
Miscellaneous