Head-to-Head Comparison of Rapid and Automated Antigen Detection Tests for the Diagnosis of SARS-CoV-2 Infection.

COVID-19 SARS-CoV-2 antigen testing automated assay manual assay

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
13 Jan 2021
Historique:
received: 10 12 2020
revised: 04 01 2021
accepted: 11 01 2021
entrez: 16 1 2021
pubmed: 17 1 2021
medline: 17 1 2021
Statut: epublish

Résumé

(1) Background: The detection of SARS-CoV-2 RNA in nasopharyngeal samples through real-time reverse transcription-polymerase chain reaction (RT-PCR) is considered the standard gold method for the diagnosis of SARS-CoV-2 infection. Antigen detection (AD) tests are more rapid, less laborious, and less expensive alternatives but still require clinical validation. (2) Methods: This study compared the clinical performance of five AD tests, including four rapid AD (RAD) tests (biotical, Panbio, Healgen, and Roche) and one automated AD test (VITROS). For that purpose, 118 (62.8%) symptomatic patients and 70 (37.2%) asymptomatic subjects were tested, and results were compared to RT-PCR. (3) Results: The performance of the RAD tests was modest and allowed us to identify RT-PCR positive patients with higher viral loads. For Ct values ≤25, the sensitivity ranged from 93.1% (95% CI: 83.3-98.1%) to 96.6% (95% CI: 88.1-99.6%), meaning that some samples with high viral loads were missed. Considering the Ct value proposed by the CDC for contagiousness (i.e., Ct values ≤33) sensitivities ranged from 76.2% (95% CI: 65.4-85.1%) to 88.8% (95% CI: 79.7-94.7%) while the specificity ranged from 96.3% (95% CI: 90.8-99.0%) to 99.1% (95% CI: 95.0-100%). The VITROS automated assay showed a 100% (95% CI: 95.5-100%) sensitivity for Ct values ≤33, and had a specificity of 100% (95% CI: 96.6-100%); (4) Conclusions: Compared to RAD tests, the VITROS assay fully aligned with RT-PCR for Ct values up to 33, which might allow a faster, easier and cheaper identification of SARS-CoV-2 contagious patients.

Identifiants

pubmed: 33450853
pii: jcm10020265
doi: 10.3390/jcm10020265
pmc: PMC7828347
pii:
doi:

Types de publication

Journal Article

Langues

eng

Commentaires et corrections

Type : CommentIn

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Auteurs

Julien Favresse (J)

Department of Laboratory Medicine, Clinique St-Luc Bouge, 5004 Namur, Belgium.
Department of Pharmacy, Namur Research Institute for Life Sciences, University of Namur, 5000 Namur, Belgium.

Constant Gillot (C)

Department of Pharmacy, Namur Research Institute for Life Sciences, University of Namur, 5000 Namur, Belgium.

Maxime Oliveira (M)

Department of Pharmacy, Namur Research Institute for Life Sciences, University of Namur, 5000 Namur, Belgium.

Julie Cadrobbi (J)

Department of Laboratory Medicine, Clinique St-Luc Bouge, 5004 Namur, Belgium.

Marc Elsen (M)

Department of Laboratory Medicine, Clinique St-Luc Bouge, 5004 Namur, Belgium.

Christine Eucher (C)

Department of Laboratory Medicine, Clinique St-Luc Bouge, 5004 Namur, Belgium.

Kim Laffineur (K)

Department of Laboratory Medicine, Clinique St-Luc Bouge, 5004 Namur, Belgium.

Catherine Rosseels (C)

Department of Laboratory Medicine, Clinique St-Luc Bouge, 5004 Namur, Belgium.

Sandrine Van Eeckhoudt (S)

Department of Internal Medicine, Clinique St-Luc Bouge, 5004 Namur, Belgium.

Jean-Baptiste Nicolas (JB)

Department of Internal Medicine, Clinique St-Luc Bouge, 5004 Namur, Belgium.

Laure Morimont (L)

Department of Pharmacy, Namur Research Institute for Life Sciences, University of Namur, 5000 Namur, Belgium.
Qualiblood S.A., 5000 Namur, Belgium.

Jean-Michel Dogné (JM)

Department of Pharmacy, Namur Research Institute for Life Sciences, University of Namur, 5000 Namur, Belgium.

Jonathan Douxfils (J)

Department of Pharmacy, Namur Research Institute for Life Sciences, University of Namur, 5000 Namur, Belgium.
Qualiblood S.A., 5000 Namur, Belgium.

Classifications MeSH