Accuracy and ease-of-use of seven point-of-care SARS-CoV-2 antigen-detecting tests: A multi-centre clinical evaluation.
View / Open Files
Authors
Krüger, Lisa J
Tanuri, Amilcar
Lindner, Andreas K
Gaeddert, Mary
Köppel, Lisa
Tobian, Frank
Brümmer, Lukas E
Klein, Julian AF
Lainati, Federica
Schnitzler, Paul
Nikolai, Olga
Mockenhaupt, Frank P
Seybold, Joachim
Corman, Victor M
Jones, Terence C
Drosten, Christian
Gottschalk, Claudius
Weber, Stefan F
Weber, Stephan
Ferreira, Orlando C
Mariani, Diana
Dos Santos Nascimento, Erika Ramos
Pereira Pinto Castineiras, Terezinha M
Galliez, Rafael Mello
Faffe, Debora Souza
Leitão, Isabela de Carvalho
Dos Santos Rodrigues, Claudia
Frauches, Thiago Silva
Nocchi, Keity J Chagas Vilela
Feitosa, Natalia Martins
Ribeiro, Sabrina Santana
Pollock, Nira R
Knorr, Britta
Welker, Andreas
de Vos, Margaretha
Sacks, JilianA
Ongarello, Stefano
Denkinger, Claudia M
Study Team
Publication Date
2022-01Journal Title
EBioMedicine
ISSN
2352-3964
Publisher
Elsevier BV
Volume
75
Number
103774
Pages
103774
Type
Article
This Version
VoR
Physical Medium
Print-Electronic
Metadata
Show full item recordCitation
Krüger, L. J., Tanuri, A., Lindner, A. K., Gaeddert, M., Köppel, L., Tobian, F., Brümmer, L. E., et al. (2022). Accuracy and ease-of-use of seven point-of-care SARS-CoV-2 antigen-detecting tests: A multi-centre clinical evaluation.. EBioMedicine, 75 (103774), 103774. https://doi.org/10.1016/j.ebiom.2021.103774
Abstract
BACKGROUND: Antigen-detecting rapid diagnostic tests (Ag-RDTs) for SARS-CoV-2 are important diagnostic tools. We assessed clinical performance and ease-of-use of seven Ag-RDTs in a prospective, manufacturer-independent, multi-centre cross-sectional diagnostic accuracy study to inform global decision makers. METHODS: Unvaccinated participants suspected of a first SARS-CoV-2 infection were recruited at six sites (Germany, Brazil). Ag-RDTs were evaluated sequentially, with collection of paired swabs for routine reverse transcription polymerase chain reaction (RT-PCR) testing and Ag-RDT testing. Performance was compared to RT-PCR overall and in sub-group analyses (viral load, symptoms, symptoms duration). To understandusability a System Usability Scale (SUS) questionnaire and ease-of-use (EoU) assessment were performed. FINDINGS: 7471 participants were included in the analysis. Sensitivities across Ag-RDTs ranged from 70·4%-90·1%, specificities were above 97·2% for all Ag-RDTs but one (93·1%).Ag-RDTs, Mologic, Bionote, Standard Q, showed diagnostic accuracy in line with WHO targets (> 80% sensitivity, > 97% specificity). All tests showed high sensitivity in the first three days after symptom onset (≥87·1%) and in individuals with viral loads≥ 6 log10SARS-CoV2 RNA copies/mL (≥ 88·7%). Usability varied, with Rapigen, Bionote and Standard Q reaching very good scores; 90, 88 and 84/100, respectively. INTERPRETATION: Variability in test performance is partially explained by variable viral loads in population evaluated over the course of the pandemic. All Ag-RDTs reach high sensitivity early in the disease and in individuals with high viral loads, supporting their role in identifying transmission relevant infections. For easy-to-use tests, performance shown will likely be maintained in routine implementation. FUNDING: Ministry of Science, Research and Arts, State of Baden-Wuerttemberg, Germany, internal funds from Heidelberg University Hospital, University Hospital Charité - Universitätsmedizin Berlin, UK Department of International Development, WHO, Unitaid.
Keywords
Antigen-detecting rapid diagnostic tests, COVID-19, SARS-CoV-2, Sensitivity, Specificity, Adult, Antigens, Viral, COVID-19, COVID-19 Serological Testing, Female, Humans, Male, Middle Aged, Point-of-Care Systems, SARS-CoV-2, Sensitivity and Specificity
Sponsorship
National Institutes of Health (NIH) (via Mount Sinai School of Medicine (MSSM)) (HHSN272201400008C)
Identifiers
External DOI: https://doi.org/10.1016/j.ebiom.2021.103774
This record's URL: https://www.repository.cam.ac.uk/handle/1810/332778
Rights
Attribution-NonCommercial-NoDerivatives 4.0 International
Licence URL: https://creativecommons.org/licenses/by-nc-nd/4.0/
Statistics
Total file downloads (since January 2020). For more information on metrics see the
IRUS guide.
Recommended or similar items
The current recommendation prototype on the Apollo Repository will be turned off on 03 February 2023. Although the pilot has been fruitful for both parties, the service provider IKVA is focusing on horizon scanning products and so the recommender service can no longer be supported. We recognise the importance of recommender services in supporting research discovery and are evaluating offerings from other service providers. If you would like to offer feedback on this decision please contact us on: support@repository.cam.ac.uk