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pISSN 2950-9114 eISSN 2950-9122
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Original Article

Lab Med Qual Assur 2024; 46(4): 208-213

Published online December 31, 2024

https://doi.org/10.15263/jlmqa.2024.46.4.208

Copyright © Korean Association of External Quality Assessment Service.

Clinical Performance Evaluation of the Ag Test for Detecting SARS-CoV-2 and Influenza A/B Viruses Using Nasopharyngeal Swabs

Myoung-Schook Yoou1,* , Ji Hun Jeong1,* , Eun-Hye Choi2 , Yuri Kim3 , Chunhwa Ihm1

1Department of Laboratory Medicine, 2Eulji Medi-Bio Research Institute, and 3Eulji Biobank, Daejeon Eulji Medical Center, Eulji University, Daejeon, Korea

Correspondence to:Chunhwa Ihm
Department of Laboratory Medicine, Daejeon Eulji Medical Center, Eulji University, 95 Dunsanseo-ro, Seo-gu, Daejeon 35233, Korea
Tel +82-42-611-3478
E-mail haneul@eulji.ac.kr

*These authors contributed equally to this study as first authors.

Received: August 22, 2024; Revised: September 12, 2024; Accepted: October 8, 2024

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background: Rapid antigen tests (RATs) are widely used in clinical settings, aiding in the prevention of infectious diseases. However, there is a lack of research on the performance of RATs that can simultaneously diagnose severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and Influenza A/B viruses. In this study, we aimed to evaluate the performance of a newly developed RAT that can detect all three pathogens at once, to assess its potential for clinical application.
Methods: Clinical performance testing was conducted using 436 nasopharyngeal swab samples collected from patients with suspected respiratory infections. The newly developed RAT was compared with realtime reverse transcription-polymerase chain reaction (rRT-PCR) results to evaluate clinical sensitivity and specificity. Additionally, concordance with two previously approved products was assessed.
Results: For patients who tested positive with rRT-PCR, the detection sensitivity of the newly developed INCLIX TRF COVID-19 & Flu A/B Ag test was 90.91% for SARS-CoV-2, 97.75% for Influenza A, and 93.00% for Influenza B, with a specificity of 100% for all three pathogens. In the concordance assessment with the existing RATs, the agreement was 99.76% (κ=0.9922) for SARS-CoV-2, 99.76% (κ=0.9927) for Influenza A, and 99.76% (κ=0.9930) for Influenza B. Compared to the existing RATs, all showed a concordance with κ >0.8.
Conclusions: The INCLIX TRF COVID-19 & Flu A/B Ag test efficiently detected antigens of SARS-CoV-2 and Influenza A/B viruses simultaneously within a short testing time of 15 minutes. Therefore, this test method, with its high sensitivity and specificity, will be highly useful for diagnosing viral infections in clinical settings.

Keywords: SARS-CoV-2, Influenza A, Influenza B, Rapid antigen test

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