Litcius/Paper detail

Clinical Evaluation of Severe Acute Respiratory Syndrome Coronavirus 2 Rapid Antigen Tests During the Omicron Wave in South Africa

Natasha Samsunder, Margaretha de Vos, Sinaye Ngcapu, Jennifer Giandhari, Lara Lewis, Ayesha B. M. Kharsany, Cherie Cawood, Túlio de Oliveira, Quarraisha Abdool Karim, Salim S. Abdool Karim, Kogieleum Naidoo, Camille Escadafal, Aida Sivro

2022The Journal of Infectious Diseases14 citationsDOIOpen Access PDF

Abstract

We evaluated the performance of nasal and nasopharyngeal Standard Q COVID-19 [coronavirus disease 2019] Ag tests (SD Biosensor) and the Panbio COVID-19 Ag Rapid Test Device (nasal; Abbott) against the Abbott RealTime severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) assay during the Omicron (clades 21M, 21K, and 21L) wave in South Africa. Overall, all evaluated tests performed well, with high sensitivity (range, 77.78%-81.42%) and excellent specificity values (>99%). The sensitivity of rapid antigen tests increased above 90% in samples with cycle threshold <20, and all 3 tests performed best within the first week after symptom onset.

Topics & Concepts

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)MedicineCoronavirus disease 2019 (COVID-19)CoronavirusRespiratory systemVirologyAntigen2019-20 coronavirus outbreakImmunologyInternal medicineDiseaseInfectious disease (medical specialty)OutbreakSARS-CoV-2 detection and testingSARS-CoV-2 and COVID-19 ResearchBiosensors and Analytical Detection
Clinical Evaluation of Severe Acute Respiratory Syndrome Coronavirus 2 Rapid Antigen Tests During the Omicron Wave in South Africa | Litcius