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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
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.
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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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