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Evaluation of the Panbio™ COVID-19 ag rapid test at an emergency room in a hospital in São Paulo, Brazil

BACKGROUND: The performance characteristics of the Panbio™ COVID-19 Ag test was evaluated at an emergency room setting against RT-PCR, considered the gold-standard for the detection of SARS-CoV-2, in São Paulo, Brazil. The study aimed to determine the sensitivity, specificity, Positive Percent Agree...

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Autores principales: Faíco-Filho, Klinger Soares, Júnior, Francisco Estivallet Finamor, Moreira, Luiz Vinícius Leão, Lins, Paulo Ricardo Gessolo, Justo, Alberto Fernando Oliveira, Bellei, Nancy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934711/
https://www.ncbi.nlm.nih.gov/pubmed/35358471
http://dx.doi.org/10.1016/j.bjid.2022.102349
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author Faíco-Filho, Klinger Soares
Júnior, Francisco Estivallet Finamor
Moreira, Luiz Vinícius Leão
Lins, Paulo Ricardo Gessolo
Justo, Alberto Fernando Oliveira
Bellei, Nancy
author_facet Faíco-Filho, Klinger Soares
Júnior, Francisco Estivallet Finamor
Moreira, Luiz Vinícius Leão
Lins, Paulo Ricardo Gessolo
Justo, Alberto Fernando Oliveira
Bellei, Nancy
author_sort Faíco-Filho, Klinger Soares
collection PubMed
description BACKGROUND: The performance characteristics of the Panbio™ COVID-19 Ag test was evaluated at an emergency room setting against RT-PCR, considered the gold-standard for the detection of SARS-CoV-2, in São Paulo, Brazil. The study aimed to determine the sensitivity, specificity, Positive Percent Agreement (PPA), and Negative Percent Agreement (NPA) as compared to RT-PCR. METHODS: Specimens from 127 suspected patients were tested by both the Panbio™ COVID-19 Ag test and by RT-PCR. RESULTS: In relation to RT-PCR using Ct values ≤ 40 as the upper limit for positivity, the Panbio™ COVID-19 Ag test showed an overall sensitivity of 84.3% (95% CI 75‒93.8%) and 98.2% (95% CI 96‒98.8%) overall specificity. For Ct values ≤ 25 (n = 37), the Panbio™ COVID-19 Ag test showed 97% sensitivity. DISCUSSION: The concordance between the Panbio™ COVID-19 Ag test and RT-PCR was 97% at Ct values below 25 but decreased at higher Ct values. For disease control, it is very important to identify infected individuals who present COVID-19 symptoms and also those who are suspected of infection due to contact with infected individuals. CONCLUSION: The Panbio™ COVID-19 Ag test is suitable for use as a diagnostic test for rapid screening of patients presenting COVID-19 symptoms, or those suspected of being infected, prior to being admitted to hospital.
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spelling pubmed-89347112022-03-21 Evaluation of the Panbio™ COVID-19 ag rapid test at an emergency room in a hospital in São Paulo, Brazil Faíco-Filho, Klinger Soares Júnior, Francisco Estivallet Finamor Moreira, Luiz Vinícius Leão Lins, Paulo Ricardo Gessolo Justo, Alberto Fernando Oliveira Bellei, Nancy Braz J Infect Dis Original Article BACKGROUND: The performance characteristics of the Panbio™ COVID-19 Ag test was evaluated at an emergency room setting against RT-PCR, considered the gold-standard for the detection of SARS-CoV-2, in São Paulo, Brazil. The study aimed to determine the sensitivity, specificity, Positive Percent Agreement (PPA), and Negative Percent Agreement (NPA) as compared to RT-PCR. METHODS: Specimens from 127 suspected patients were tested by both the Panbio™ COVID-19 Ag test and by RT-PCR. RESULTS: In relation to RT-PCR using Ct values ≤ 40 as the upper limit for positivity, the Panbio™ COVID-19 Ag test showed an overall sensitivity of 84.3% (95% CI 75‒93.8%) and 98.2% (95% CI 96‒98.8%) overall specificity. For Ct values ≤ 25 (n = 37), the Panbio™ COVID-19 Ag test showed 97% sensitivity. DISCUSSION: The concordance between the Panbio™ COVID-19 Ag test and RT-PCR was 97% at Ct values below 25 but decreased at higher Ct values. For disease control, it is very important to identify infected individuals who present COVID-19 symptoms and also those who are suspected of infection due to contact with infected individuals. CONCLUSION: The Panbio™ COVID-19 Ag test is suitable for use as a diagnostic test for rapid screening of patients presenting COVID-19 symptoms, or those suspected of being infected, prior to being admitted to hospital. Elsevier 2022-03-21 /pmc/articles/PMC8934711/ /pubmed/35358471 http://dx.doi.org/10.1016/j.bjid.2022.102349 Text en © 2022 Sociedade Brasileira de Infectologia. Published by Elsevier España, S.L.U. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Faíco-Filho, Klinger Soares
Júnior, Francisco Estivallet Finamor
Moreira, Luiz Vinícius Leão
Lins, Paulo Ricardo Gessolo
Justo, Alberto Fernando Oliveira
Bellei, Nancy
Evaluation of the Panbio™ COVID-19 ag rapid test at an emergency room in a hospital in São Paulo, Brazil
title Evaluation of the Panbio™ COVID-19 ag rapid test at an emergency room in a hospital in São Paulo, Brazil
title_full Evaluation of the Panbio™ COVID-19 ag rapid test at an emergency room in a hospital in São Paulo, Brazil
title_fullStr Evaluation of the Panbio™ COVID-19 ag rapid test at an emergency room in a hospital in São Paulo, Brazil
title_full_unstemmed Evaluation of the Panbio™ COVID-19 ag rapid test at an emergency room in a hospital in São Paulo, Brazil
title_short Evaluation of the Panbio™ COVID-19 ag rapid test at an emergency room in a hospital in São Paulo, Brazil
title_sort evaluation of the panbio™ covid-19 ag rapid test at an emergency room in a hospital in são paulo, brazil
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934711/
https://www.ncbi.nlm.nih.gov/pubmed/35358471
http://dx.doi.org/10.1016/j.bjid.2022.102349
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