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Repurposing Positive SARS-CoV-2 Antigen Test Devices for Variant Tracking
From the very beginning of the SARS-CoV-2 pandemic, one of the very few common opinions was that to control the expansion of the virus as many as the possible test had to be done. Antigen tests, being affordable and easy and fast to use, represented a great opportunity to expand the testing capaciti...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315323/ https://www.ncbi.nlm.nih.gov/pubmed/35881313 http://dx.doi.org/10.1007/s00284-022-02973-8 |
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author | Urrutikoetxea-Gutierrez, Mikel Nieto Toboso, Maria Carmen Ugalde Zarraga, Estibaliz Macho Aizpurua, Mikele Diaz de Tuesta del Arco, Jose Luis |
author_facet | Urrutikoetxea-Gutierrez, Mikel Nieto Toboso, Maria Carmen Ugalde Zarraga, Estibaliz Macho Aizpurua, Mikele Diaz de Tuesta del Arco, Jose Luis |
author_sort | Urrutikoetxea-Gutierrez, Mikel |
collection | PubMed |
description | From the very beginning of the SARS-CoV-2 pandemic, one of the very few common opinions was that to control the expansion of the virus as many as the possible test had to be done. Antigen tests, being affordable and easy and fast to use, represented a great opportunity to expand the testing capacities of many healthcare systems. However, in 2021 with the appearance of the new SARS-CoV-2 variants, variant tracking strategies had to be implemented, which often included needing a second test to determine the variant of the patients diagnosed with antigen tests or not taking these samples into consideration at all. Therefore, we proposed recovering the positive antigen test devices to include them in our routine variant tracking strategy. The recovered positive antigen test devices obtained from 1st April 2021 to 15the January 2022 were analysed following the variant tracking protocol in force. The results obtained were compared to the positive samples detected by RT-PCR which were processed for variant tracking during the same period. 21,304 samples were processed, 6297 from the recovered positive antigen devices and 15,007 from the standard nasopharyngeal swabs. Only 773 (3.63%) samples were no conclusive, 104 (1.65%) from the recovered antigen devices and 669 (4.46%) from the RT-PCR positive group. This difference was statistically significant (p < 0.01). Taking this into account the proposed method is suitable and very recommendable, as it is an important measure to have a better and immediate picture of the circulating variants in every community. |
format | Online Article Text |
id | pubmed-9315323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-93153232022-07-26 Repurposing Positive SARS-CoV-2 Antigen Test Devices for Variant Tracking Urrutikoetxea-Gutierrez, Mikel Nieto Toboso, Maria Carmen Ugalde Zarraga, Estibaliz Macho Aizpurua, Mikele Diaz de Tuesta del Arco, Jose Luis Curr Microbiol Short Communication From the very beginning of the SARS-CoV-2 pandemic, one of the very few common opinions was that to control the expansion of the virus as many as the possible test had to be done. Antigen tests, being affordable and easy and fast to use, represented a great opportunity to expand the testing capacities of many healthcare systems. However, in 2021 with the appearance of the new SARS-CoV-2 variants, variant tracking strategies had to be implemented, which often included needing a second test to determine the variant of the patients diagnosed with antigen tests or not taking these samples into consideration at all. Therefore, we proposed recovering the positive antigen test devices to include them in our routine variant tracking strategy. The recovered positive antigen test devices obtained from 1st April 2021 to 15the January 2022 were analysed following the variant tracking protocol in force. The results obtained were compared to the positive samples detected by RT-PCR which were processed for variant tracking during the same period. 21,304 samples were processed, 6297 from the recovered positive antigen devices and 15,007 from the standard nasopharyngeal swabs. Only 773 (3.63%) samples were no conclusive, 104 (1.65%) from the recovered antigen devices and 669 (4.46%) from the RT-PCR positive group. This difference was statistically significant (p < 0.01). Taking this into account the proposed method is suitable and very recommendable, as it is an important measure to have a better and immediate picture of the circulating variants in every community. Springer US 2022-07-26 2022 /pmc/articles/PMC9315323/ /pubmed/35881313 http://dx.doi.org/10.1007/s00284-022-02973-8 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Short Communication Urrutikoetxea-Gutierrez, Mikel Nieto Toboso, Maria Carmen Ugalde Zarraga, Estibaliz Macho Aizpurua, Mikele Diaz de Tuesta del Arco, Jose Luis Repurposing Positive SARS-CoV-2 Antigen Test Devices for Variant Tracking |
title | Repurposing Positive SARS-CoV-2 Antigen Test Devices for Variant Tracking |
title_full | Repurposing Positive SARS-CoV-2 Antigen Test Devices for Variant Tracking |
title_fullStr | Repurposing Positive SARS-CoV-2 Antigen Test Devices for Variant Tracking |
title_full_unstemmed | Repurposing Positive SARS-CoV-2 Antigen Test Devices for Variant Tracking |
title_short | Repurposing Positive SARS-CoV-2 Antigen Test Devices for Variant Tracking |
title_sort | repurposing positive sars-cov-2 antigen test devices for variant tracking |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315323/ https://www.ncbi.nlm.nih.gov/pubmed/35881313 http://dx.doi.org/10.1007/s00284-022-02973-8 |
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