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Evaluation of the practicability of a finger-stick whole-blood SARS-Cov-2 self-test adapted for the general population
BACKGROUND: COVID-19 (COronaVIrus Disease 2019) is an infectious respiratory disease caused by the novel SARS-CoV-2 virus. Point of Care (POC) tests have been developed to detect specific antibodies, IgG and IgM, to SARS-CoV-2 virus in human whole blood. They need to be easily usable by the general...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842899/ https://www.ncbi.nlm.nih.gov/pubmed/33508007 http://dx.doi.org/10.1371/journal.pone.0245848 |
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author | Prazuck, Thierry Phan Van, Jean Sinturel, Florence Levray, Frederique Elie, Allan Camera, Denise Pialoux, Gilles |
author_facet | Prazuck, Thierry Phan Van, Jean Sinturel, Florence Levray, Frederique Elie, Allan Camera, Denise Pialoux, Gilles |
author_sort | Prazuck, Thierry |
collection | PubMed |
description | BACKGROUND: COVID-19 (COronaVIrus Disease 2019) is an infectious respiratory disease caused by the novel SARS-CoV-2 virus. Point of Care (POC) tests have been developed to detect specific antibodies, IgG and IgM, to SARS-CoV-2 virus in human whole blood. They need to be easily usable by the general population in order to alleviate the lockdown that many countries have initiated in response to the growing COVID-19 pandemic. A real-life study has been conducted in order to evaluate the performance of the COVID-PRESTO(®) POC test and the results were recently published. Even if this test showed very high sensitivity and specificity in a laboratory setting when used by trained professionals, it needs to be further evaluated for practicability when used by the general public in order to be approved by health authorities for in-home use. METHODS: 143 participants were recruited between March 2020 and April 2020 among non-medical populations in central France (nuclear plant workers, individuals attending the Orleans University Hospital vaccination clinic and Orleans University Hospital non-medical staff). Instructions for use, with or without a tutorial video, were made available to the volunteers. Two separate objectives were pursued: evaluation of the capability of participants to obtain an interpretable result, and evaluation of the users’ ability to read the results. RESULTS: 88.4% of the test users judged the instructions for use leaflet to be clear and understandable. 99.3% of the users obtained a valid result and, according to the supervisors, 92.7% of the tests were properly performed by the users. Overall, 95% of the users gave positive feedback on the COVID PRESTO(®) as a potential self-test. Neither age nor education had an influence. CONCLUSION: COVID-PRESTO(®) was successfully used by an overwhelming majority of participants and its use was judged very satisfactory, therefore showing promising potential as a self-test to be used by the general population. This POC test can become an easy-to-use tool to help detect whether individuals are protected or not, particularly in the context of a second wave or a mass vaccination program. |
format | Online Article Text |
id | pubmed-7842899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-78428992021-02-02 Evaluation of the practicability of a finger-stick whole-blood SARS-Cov-2 self-test adapted for the general population Prazuck, Thierry Phan Van, Jean Sinturel, Florence Levray, Frederique Elie, Allan Camera, Denise Pialoux, Gilles PLoS One Research Article BACKGROUND: COVID-19 (COronaVIrus Disease 2019) is an infectious respiratory disease caused by the novel SARS-CoV-2 virus. Point of Care (POC) tests have been developed to detect specific antibodies, IgG and IgM, to SARS-CoV-2 virus in human whole blood. They need to be easily usable by the general population in order to alleviate the lockdown that many countries have initiated in response to the growing COVID-19 pandemic. A real-life study has been conducted in order to evaluate the performance of the COVID-PRESTO(®) POC test and the results were recently published. Even if this test showed very high sensitivity and specificity in a laboratory setting when used by trained professionals, it needs to be further evaluated for practicability when used by the general public in order to be approved by health authorities for in-home use. METHODS: 143 participants were recruited between March 2020 and April 2020 among non-medical populations in central France (nuclear plant workers, individuals attending the Orleans University Hospital vaccination clinic and Orleans University Hospital non-medical staff). Instructions for use, with or without a tutorial video, were made available to the volunteers. Two separate objectives were pursued: evaluation of the capability of participants to obtain an interpretable result, and evaluation of the users’ ability to read the results. RESULTS: 88.4% of the test users judged the instructions for use leaflet to be clear and understandable. 99.3% of the users obtained a valid result and, according to the supervisors, 92.7% of the tests were properly performed by the users. Overall, 95% of the users gave positive feedback on the COVID PRESTO(®) as a potential self-test. Neither age nor education had an influence. CONCLUSION: COVID-PRESTO(®) was successfully used by an overwhelming majority of participants and its use was judged very satisfactory, therefore showing promising potential as a self-test to be used by the general population. This POC test can become an easy-to-use tool to help detect whether individuals are protected or not, particularly in the context of a second wave or a mass vaccination program. Public Library of Science 2021-01-28 /pmc/articles/PMC7842899/ /pubmed/33508007 http://dx.doi.org/10.1371/journal.pone.0245848 Text en © 2021 Prazuck et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Prazuck, Thierry Phan Van, Jean Sinturel, Florence Levray, Frederique Elie, Allan Camera, Denise Pialoux, Gilles Evaluation of the practicability of a finger-stick whole-blood SARS-Cov-2 self-test adapted for the general population |
title | Evaluation of the practicability of a finger-stick whole-blood SARS-Cov-2 self-test adapted for the general population |
title_full | Evaluation of the practicability of a finger-stick whole-blood SARS-Cov-2 self-test adapted for the general population |
title_fullStr | Evaluation of the practicability of a finger-stick whole-blood SARS-Cov-2 self-test adapted for the general population |
title_full_unstemmed | Evaluation of the practicability of a finger-stick whole-blood SARS-Cov-2 self-test adapted for the general population |
title_short | Evaluation of the practicability of a finger-stick whole-blood SARS-Cov-2 self-test adapted for the general population |
title_sort | evaluation of the practicability of a finger-stick whole-blood sars-cov-2 self-test adapted for the general population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842899/ https://www.ncbi.nlm.nih.gov/pubmed/33508007 http://dx.doi.org/10.1371/journal.pone.0245848 |
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