Virus variant-specific clinical performance of a SARS-CoV-2 rapid antigen test with focus on Omicron variants of concern.

Antigen rapid diagnostic test COVID-19 Cycle threshold Limit of detection Omicron variant RT-PCR SARS-CoV-2 Sensitivity Variants of concern Viral load

Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 22 12 2022
revised: 25 04 2023
accepted: 06 05 2023
medline: 23 10 2023
pubmed: 15 5 2023
entrez: 14 5 2023
Statut: ppublish

Résumé

Antigen rapid diagnostic tests (Ag-RDTs) play an important role in the diagnosis of SARS-CoV-2. They are easier, quicker, and less expensive than the 'reference standard' RT-PCR and therefore widely in use. Reliable clinical data with respect to Ag-RDT performance in SARS-CoV-2 Omicron variants of concern (VOCs) are limited. Consequently, the objective of this study was to determine the impact different VOCs-especially Omicron-have on the clinical performance of an Ag-RDT. We compared the clinical performance of the Sofia SARS-CoV-2 Ag-RDT to RT-PCR in a real-world, single-centre study in a clinical point-of-care setting in patients admitted to a large hospital via the emergency department from 2 November 2020 to 4 September 2022. Among 38 434 Ag-RDT/RT-PCR tandems taken, 1528 yielded a SARS-CoV-2 positive RT-PCR test result, with a prevalence of 4.0% (95% CI, 3.8-4.2). Overall sensitivity of the Ag-RDT was 63.7% (95% CI, 61.3-66.1) and overall specificity was 99.6% (95% CI, 99.5-99.6). Ag-RDT sensitivity was dependent on viral load (VL), because the sensitivity increased to 93.2% (95% CI, 91.5-94.6) in samples with a VL > 10 Ag-RDT sensitivity for detection of patients with lower VLs and with Omicron-VOC is reduced, limiting the effectiveness of Ag-RDTs. However, Ag-RDTs are still an unreplaceable tool for widely available, quick, and inexpensive point-of-care SARS-CoV-2 diagnostics.

Identifiants

pubmed: 37182639
pii: S1198-743X(23)00233-1
doi: 10.1016/j.cmi.2023.05.009
pmc: PMC10181871
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1085.e1-1085.e8

Informations de copyright

Copyright © 2023. Published by Elsevier Ltd.

Auteurs

Linus Bornemann (L)

Institute of Virology, University Medical Centre and Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Olaf Kaup (O)

Institute of Laboratory Medicine, Microbiology and Transfusion Medicine, Campus Bielefeld Hospital, University Hospital OWL, Bielefeld, Germany.

Johannes Kleideiter (J)

Department of Clinical Hygiene, Campus Bielefeld Hospital, University Hospital OWL, Bielefeld, Germany.

Bertram Ruprecht (B)

Department of Pneumology and Respiratory Medicine, Campus Bielefeld Hospital, University Hospital OWL, Bielefeld, Germany.

Annika Hoyer (A)

Institute of Biostatistics and Medical Biometry, University Medical School OWL, University Bielefeld, Bielefeld, Germany.

Marcus Panning (M)

Institute of Virology, University Medical Centre and Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Reinhard Bornemann (R)

Institute of Population Medicine and Health Services, School of Public Health University Bielefeld, Bielefeld, Germany.

Michael Wehmeier (M)

Institute of Laboratory Medicine, Microbiology and Transfusion Medicine, Campus Bielefeld Hospital, University Hospital OWL, Bielefeld, Germany. Electronic address: michael.wehmeier@klinikumbielefeld.de.

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