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Validez interna de una prueba rápida de detección de antígenos COVID-19 en una residencia de mayores
INTRODUCTION: RT-qPCR is the reference test for the detection of SARS-CoV-2 infection, however, rapid antigen detection tests (RADT) are now available. In this work, the internal validity of the RADT was evaluated in the context of an outbreak in a nursing home. METHODS: Nasopharyngeal exudate sampl...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedad Española de Médicos de Atención Primaria (SEMERGEN). Published by Elsevier España, S.L.U.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8078913/ https://www.ncbi.nlm.nih.gov/pubmed/34034982 http://dx.doi.org/10.1016/j.semerg.2021.04.003 |
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author | Diez Flecha, C. Rivero Rodríguez, A.M. Fernández-Villa, T. Fernández García, P. Ferreira de Jesús, J.L. Sánchez Antolín, G. |
author_facet | Diez Flecha, C. Rivero Rodríguez, A.M. Fernández-Villa, T. Fernández García, P. Ferreira de Jesús, J.L. Sánchez Antolín, G. |
author_sort | Diez Flecha, C. |
collection | PubMed |
description | INTRODUCTION: RT-qPCR is the reference test for the detection of SARS-CoV-2 infection, however, rapid antigen detection tests (RADT) are now available. In this work, the internal validity of the RADT was evaluated in the context of an outbreak in a nursing home. METHODS: Nasopharyngeal exudate samples were analyzed by RADT and RT-qPCR from 61 residents of a nursing home. The sensitivity and specificity of RADT with respect to RT-qPCR was calculated. RESULTS: Specificity was 100% (95% CI 54.1-100.0), while sensitivity in asymptomatic people was 70.3% (95% CI 53.0-84.1) and in symptomatic people 83.3% (95% CI 51.6-97.9). CONCLUSIONS: The RADTs are sufficiently sensitive and specific to be used as screening tests in nursing homes, especially in situations of outbreaks or suspected outbreaks due to the presence of symptoms. |
format | Online Article Text |
id | pubmed-8078913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Sociedad Española de Médicos de Atención Primaria (SEMERGEN). Published by Elsevier España, S.L.U. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80789132021-04-28 Validez interna de una prueba rápida de detección de antígenos COVID-19 en una residencia de mayores Diez Flecha, C. Rivero Rodríguez, A.M. Fernández-Villa, T. Fernández García, P. Ferreira de Jesús, J.L. Sánchez Antolín, G. Semergen Original INTRODUCTION: RT-qPCR is the reference test for the detection of SARS-CoV-2 infection, however, rapid antigen detection tests (RADT) are now available. In this work, the internal validity of the RADT was evaluated in the context of an outbreak in a nursing home. METHODS: Nasopharyngeal exudate samples were analyzed by RADT and RT-qPCR from 61 residents of a nursing home. The sensitivity and specificity of RADT with respect to RT-qPCR was calculated. RESULTS: Specificity was 100% (95% CI 54.1-100.0), while sensitivity in asymptomatic people was 70.3% (95% CI 53.0-84.1) and in symptomatic people 83.3% (95% CI 51.6-97.9). CONCLUSIONS: The RADTs are sufficiently sensitive and specific to be used as screening tests in nursing homes, especially in situations of outbreaks or suspected outbreaks due to the presence of symptoms. Sociedad Española de Médicos de Atención Primaria (SEMERGEN). Published by Elsevier España, S.L.U. 2021 2021-04-27 /pmc/articles/PMC8078913/ /pubmed/34034982 http://dx.doi.org/10.1016/j.semerg.2021.04.003 Text en © 2021 Sociedad Española de Médicos de Atención Primaria (SEMERGEN). Published by Elsevier España, S.L.U. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Original Diez Flecha, C. Rivero Rodríguez, A.M. Fernández-Villa, T. Fernández García, P. Ferreira de Jesús, J.L. Sánchez Antolín, G. Validez interna de una prueba rápida de detección de antígenos COVID-19 en una residencia de mayores |
title | Validez interna de una prueba rápida de detección de antígenos COVID-19 en una residencia de mayores |
title_full | Validez interna de una prueba rápida de detección de antígenos COVID-19 en una residencia de mayores |
title_fullStr | Validez interna de una prueba rápida de detección de antígenos COVID-19 en una residencia de mayores |
title_full_unstemmed | Validez interna de una prueba rápida de detección de antígenos COVID-19 en una residencia de mayores |
title_short | Validez interna de una prueba rápida de detección de antígenos COVID-19 en una residencia de mayores |
title_sort | validez interna de una prueba rápida de detección de antígenos covid-19 en una residencia de mayores |
topic | Original |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8078913/ https://www.ncbi.nlm.nih.gov/pubmed/34034982 http://dx.doi.org/10.1016/j.semerg.2021.04.003 |
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