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Evaluation of COVID-19 Antigen Fluorescence Immunoassay Test for Rapid Detection of SARS-CoV-2
INTRODUCTION: Tests detecting SARS-CoV-2-specific antigen have recently been developed, and many of them are now commercially available. However, the real-world performance of these assays is uncertain; therefore, their validation is important. In this study, we have evaluated the performance of STA...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213088/ https://www.ncbi.nlm.nih.gov/pubmed/34194176 http://dx.doi.org/10.4103/jgid.jgid_316_20 |
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author | Kiro, Vandana Vijayeta Gupta, Ankesh Singh, Parul Sharad, Neha Khurana, Surbhi Prakash, S Dar, Lalit Malhotra, Rajesh Wig, Naveet Kumar, Arvind Trikha, Anjan Mathur, Purva |
author_facet | Kiro, Vandana Vijayeta Gupta, Ankesh Singh, Parul Sharad, Neha Khurana, Surbhi Prakash, S Dar, Lalit Malhotra, Rajesh Wig, Naveet Kumar, Arvind Trikha, Anjan Mathur, Purva |
author_sort | Kiro, Vandana Vijayeta |
collection | PubMed |
description | INTRODUCTION: Tests detecting SARS-CoV-2-specific antigen have recently been developed, and many of them are now commercially available. However, the real-world performance of these assays is uncertain; therefore, their validation is important. In this study, we have evaluated the performance of STANDARD F COVID-19 antigen fluorescence immunoassay (FIA) kit. METHODS: Nasopharyngeal samples collected from patients were subjected to the test as per manufacturer's instructions. The performance of the kit was compared with the gold standard real-time polymerase chain reaction. RESULTS: A total of 354 patients were tested with STANDARD F COVID-19 antigen FIA test kit. The overall sensitivity, specificity, positive predictive value, and negative predictive value of this test were found to be 38%, 99%, 96.2%, and 72%, respectively, with a diagnostic accuracy of 75.7%. CONCLUSION: STANDARD F COVID-19 antigen FIA showed high specificity and positive predictive value but low sensitivity and negative predictive value. |
format | Online Article Text |
id | pubmed-8213088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-82130882021-06-29 Evaluation of COVID-19 Antigen Fluorescence Immunoassay Test for Rapid Detection of SARS-CoV-2 Kiro, Vandana Vijayeta Gupta, Ankesh Singh, Parul Sharad, Neha Khurana, Surbhi Prakash, S Dar, Lalit Malhotra, Rajesh Wig, Naveet Kumar, Arvind Trikha, Anjan Mathur, Purva J Glob Infect Dis Microbiology Report INTRODUCTION: Tests detecting SARS-CoV-2-specific antigen have recently been developed, and many of them are now commercially available. However, the real-world performance of these assays is uncertain; therefore, their validation is important. In this study, we have evaluated the performance of STANDARD F COVID-19 antigen fluorescence immunoassay (FIA) kit. METHODS: Nasopharyngeal samples collected from patients were subjected to the test as per manufacturer's instructions. The performance of the kit was compared with the gold standard real-time polymerase chain reaction. RESULTS: A total of 354 patients were tested with STANDARD F COVID-19 antigen FIA test kit. The overall sensitivity, specificity, positive predictive value, and negative predictive value of this test were found to be 38%, 99%, 96.2%, and 72%, respectively, with a diagnostic accuracy of 75.7%. CONCLUSION: STANDARD F COVID-19 antigen FIA showed high specificity and positive predictive value but low sensitivity and negative predictive value. Wolters Kluwer - Medknow 2021-05-31 /pmc/articles/PMC8213088/ /pubmed/34194176 http://dx.doi.org/10.4103/jgid.jgid_316_20 Text en Copyright: © 2021 Journal of Global Infectious Diseases https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Microbiology Report Kiro, Vandana Vijayeta Gupta, Ankesh Singh, Parul Sharad, Neha Khurana, Surbhi Prakash, S Dar, Lalit Malhotra, Rajesh Wig, Naveet Kumar, Arvind Trikha, Anjan Mathur, Purva Evaluation of COVID-19 Antigen Fluorescence Immunoassay Test for Rapid Detection of SARS-CoV-2 |
title | Evaluation of COVID-19 Antigen Fluorescence Immunoassay Test for Rapid Detection of SARS-CoV-2 |
title_full | Evaluation of COVID-19 Antigen Fluorescence Immunoassay Test for Rapid Detection of SARS-CoV-2 |
title_fullStr | Evaluation of COVID-19 Antigen Fluorescence Immunoassay Test for Rapid Detection of SARS-CoV-2 |
title_full_unstemmed | Evaluation of COVID-19 Antigen Fluorescence Immunoassay Test for Rapid Detection of SARS-CoV-2 |
title_short | Evaluation of COVID-19 Antigen Fluorescence Immunoassay Test for Rapid Detection of SARS-CoV-2 |
title_sort | evaluation of covid-19 antigen fluorescence immunoassay test for rapid detection of sars-cov-2 |
topic | Microbiology Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213088/ https://www.ncbi.nlm.nih.gov/pubmed/34194176 http://dx.doi.org/10.4103/jgid.jgid_316_20 |
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