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Virus variant–specific clinical performance of SARS coronavirus two rapid antigen tests in point-of-care use, from November 2020 to January 2022

OBJECTIVES: Antigen rapid diagnostic tests (RDTs) for SARS coronavirus 2 (SARS-CoV-2) are quick, widely available, and inexpensive. Consequently, RDTs have been established as an alternative and additional diagnostic strategy to quantitative reverse transcription polymerase chain reaction (RT-qPCR)....

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Autores principales: Wagenhäuser, Isabell, Knies, Kerstin, Hofmann, Daniela, Rauschenberger, Vera, Eisenmann, Michael, Reusch, Julia, Gabel, Alexander, Flemming, Sven, Andres, Oliver, Petri, Nils, Topp, Max S., Papsdorf, Michael, McDonogh, Miriam, Verma-Führing, Raoul, Scherzad, Agmal, Zeller, Daniel, Böhm, Hartmut, Gesierich, Anja, Seitz, Anna K., Kiderlen, Michael, Gawlik, Micha, Taurines, Regina, Wurmb, Thomas, Ernestus, Ralf-Ingo, Forster, Johannes, Weismann, Dirk, Weißbrich, Benedikt, Dölken, Lars, Liese, Johannes, Kaderali, Lars, Kurzai, Oliver, Vogel, Ulrich, Krone, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9398563/
https://www.ncbi.nlm.nih.gov/pubmed/36028089
http://dx.doi.org/10.1016/j.cmi.2022.08.006
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author Wagenhäuser, Isabell
Knies, Kerstin
Hofmann, Daniela
Rauschenberger, Vera
Eisenmann, Michael
Reusch, Julia
Gabel, Alexander
Flemming, Sven
Andres, Oliver
Petri, Nils
Topp, Max S.
Papsdorf, Michael
McDonogh, Miriam
Verma-Führing, Raoul
Scherzad, Agmal
Zeller, Daniel
Böhm, Hartmut
Gesierich, Anja
Seitz, Anna K.
Kiderlen, Michael
Gawlik, Micha
Taurines, Regina
Wurmb, Thomas
Ernestus, Ralf-Ingo
Forster, Johannes
Weismann, Dirk
Weißbrich, Benedikt
Dölken, Lars
Liese, Johannes
Kaderali, Lars
Kurzai, Oliver
Vogel, Ulrich
Krone, Manuel
author_facet Wagenhäuser, Isabell
Knies, Kerstin
Hofmann, Daniela
Rauschenberger, Vera
Eisenmann, Michael
Reusch, Julia
Gabel, Alexander
Flemming, Sven
Andres, Oliver
Petri, Nils
Topp, Max S.
Papsdorf, Michael
McDonogh, Miriam
Verma-Führing, Raoul
Scherzad, Agmal
Zeller, Daniel
Böhm, Hartmut
Gesierich, Anja
Seitz, Anna K.
Kiderlen, Michael
Gawlik, Micha
Taurines, Regina
Wurmb, Thomas
Ernestus, Ralf-Ingo
Forster, Johannes
Weismann, Dirk
Weißbrich, Benedikt
Dölken, Lars
Liese, Johannes
Kaderali, Lars
Kurzai, Oliver
Vogel, Ulrich
Krone, Manuel
author_sort Wagenhäuser, Isabell
collection PubMed
description OBJECTIVES: Antigen rapid diagnostic tests (RDTs) for SARS coronavirus 2 (SARS-CoV-2) are quick, widely available, and inexpensive. Consequently, RDTs have been established as an alternative and additional diagnostic strategy to quantitative reverse transcription polymerase chain reaction (RT-qPCR). However, reliable clinical and large-scale performance data specific to a SARS-CoV-2 virus variant of concern (VOC) are limited, especially for the Omicron VOC. The aim of this study was to compare RDT performance among different VOCs. METHODS: This single-centre prospective performance assessment compared RDTs from three manufacturers (NADAL, Panbio, MEDsan) with RT-qPCR including deduced standardized viral load from oropharyngeal swabs for detection of SARS-CoV-2 in a clinical point-of-care setting from November 2020 to January 2022. RESULTS: Among 35 479 RDT/RT-qPCR tandems taken from 26 940 individuals, 164 of the 426 SARS-CoV-2 positive samples tested true positive with an RDT corresponding to an RDT sensitivity of 38.50% (95% CI, 34.00–43.20%), with an overall specificity of 99.67% (95% CI, 99.60–99.72%). RDT sensitivity depended on viral load, with decreasing sensitivity accompanied by descending viral load. VOC-dependent sensitivity assessment showed a sensitivity of 42.86% (95% CI, 32.82–53.52%) for the wild-type SARS-CoV-2, 43.42% (95% CI, 32.86–54.61%) for the Alpha VOC, 37.67% (95% CI, 30.22–45.75%) for the Delta VOC, and 33.67% (95% CI, 25.09–43.49%) for the Omicron VOC. Sensitivity in samples with high viral loads of ≥10(6) SARS-CoV-2 RNA copies per mL was significantly lower in the Omicron VOC (50.00%; 95% CI, 36.12–63.88%) than in the wild-type SARS-CoV-2 (79.31%; 95% CI, 61.61–90.15%; p 0.015). DISCUSSION: RDT sensitivity for detection of the Omicron VOC is reduced in individuals infected with a high viral load, which curtails the effectiveness of RDTs. This aspect furthert: limits the use of RDTs, although RDTs are still an irreplaceable diagnostic tool for rapid, economic point-of-care and extensive SARS-CoV-2 screening.
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spelling pubmed-93985632022-08-24 Virus variant–specific clinical performance of SARS coronavirus two rapid antigen tests in point-of-care use, from November 2020 to January 2022 Wagenhäuser, Isabell Knies, Kerstin Hofmann, Daniela Rauschenberger, Vera Eisenmann, Michael Reusch, Julia Gabel, Alexander Flemming, Sven Andres, Oliver Petri, Nils Topp, Max S. Papsdorf, Michael McDonogh, Miriam Verma-Führing, Raoul Scherzad, Agmal Zeller, Daniel Böhm, Hartmut Gesierich, Anja Seitz, Anna K. Kiderlen, Michael Gawlik, Micha Taurines, Regina Wurmb, Thomas Ernestus, Ralf-Ingo Forster, Johannes Weismann, Dirk Weißbrich, Benedikt Dölken, Lars Liese, Johannes Kaderali, Lars Kurzai, Oliver Vogel, Ulrich Krone, Manuel Clin Microbiol Infect Original Article OBJECTIVES: Antigen rapid diagnostic tests (RDTs) for SARS coronavirus 2 (SARS-CoV-2) are quick, widely available, and inexpensive. Consequently, RDTs have been established as an alternative and additional diagnostic strategy to quantitative reverse transcription polymerase chain reaction (RT-qPCR). However, reliable clinical and large-scale performance data specific to a SARS-CoV-2 virus variant of concern (VOC) are limited, especially for the Omicron VOC. The aim of this study was to compare RDT performance among different VOCs. METHODS: This single-centre prospective performance assessment compared RDTs from three manufacturers (NADAL, Panbio, MEDsan) with RT-qPCR including deduced standardized viral load from oropharyngeal swabs for detection of SARS-CoV-2 in a clinical point-of-care setting from November 2020 to January 2022. RESULTS: Among 35 479 RDT/RT-qPCR tandems taken from 26 940 individuals, 164 of the 426 SARS-CoV-2 positive samples tested true positive with an RDT corresponding to an RDT sensitivity of 38.50% (95% CI, 34.00–43.20%), with an overall specificity of 99.67% (95% CI, 99.60–99.72%). RDT sensitivity depended on viral load, with decreasing sensitivity accompanied by descending viral load. VOC-dependent sensitivity assessment showed a sensitivity of 42.86% (95% CI, 32.82–53.52%) for the wild-type SARS-CoV-2, 43.42% (95% CI, 32.86–54.61%) for the Alpha VOC, 37.67% (95% CI, 30.22–45.75%) for the Delta VOC, and 33.67% (95% CI, 25.09–43.49%) for the Omicron VOC. Sensitivity in samples with high viral loads of ≥10(6) SARS-CoV-2 RNA copies per mL was significantly lower in the Omicron VOC (50.00%; 95% CI, 36.12–63.88%) than in the wild-type SARS-CoV-2 (79.31%; 95% CI, 61.61–90.15%; p 0.015). DISCUSSION: RDT sensitivity for detection of the Omicron VOC is reduced in individuals infected with a high viral load, which curtails the effectiveness of RDTs. This aspect furthert: limits the use of RDTs, although RDTs are still an irreplaceable diagnostic tool for rapid, economic point-of-care and extensive SARS-CoV-2 screening. European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. 2023-02 2022-08-24 /pmc/articles/PMC9398563/ /pubmed/36028089 http://dx.doi.org/10.1016/j.cmi.2022.08.006 Text en © 2022 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. 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 Article
Wagenhäuser, Isabell
Knies, Kerstin
Hofmann, Daniela
Rauschenberger, Vera
Eisenmann, Michael
Reusch, Julia
Gabel, Alexander
Flemming, Sven
Andres, Oliver
Petri, Nils
Topp, Max S.
Papsdorf, Michael
McDonogh, Miriam
Verma-Führing, Raoul
Scherzad, Agmal
Zeller, Daniel
Böhm, Hartmut
Gesierich, Anja
Seitz, Anna K.
Kiderlen, Michael
Gawlik, Micha
Taurines, Regina
Wurmb, Thomas
Ernestus, Ralf-Ingo
Forster, Johannes
Weismann, Dirk
Weißbrich, Benedikt
Dölken, Lars
Liese, Johannes
Kaderali, Lars
Kurzai, Oliver
Vogel, Ulrich
Krone, Manuel
Virus variant–specific clinical performance of SARS coronavirus two rapid antigen tests in point-of-care use, from November 2020 to January 2022
title Virus variant–specific clinical performance of SARS coronavirus two rapid antigen tests in point-of-care use, from November 2020 to January 2022
title_full Virus variant–specific clinical performance of SARS coronavirus two rapid antigen tests in point-of-care use, from November 2020 to January 2022
title_fullStr Virus variant–specific clinical performance of SARS coronavirus two rapid antigen tests in point-of-care use, from November 2020 to January 2022
title_full_unstemmed Virus variant–specific clinical performance of SARS coronavirus two rapid antigen tests in point-of-care use, from November 2020 to January 2022
title_short Virus variant–specific clinical performance of SARS coronavirus two rapid antigen tests in point-of-care use, from November 2020 to January 2022
title_sort virus variant–specific clinical performance of sars coronavirus two rapid antigen tests in point-of-care use, from november 2020 to january 2022
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9398563/
https://www.ncbi.nlm.nih.gov/pubmed/36028089
http://dx.doi.org/10.1016/j.cmi.2022.08.006
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