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. 2023 Jul 10;34(2):123–141.

Table 2.

Summary of the diagnostic performance of the studies which explored the performance of Quidel Sofia SARS antigen Fluorescent Immunoassay (FIA) for diagnosing acute SARS-CoV-2 infections

Cohort AUC (SE) Sensitivity (95%CI) Specificity (95%CI)
All samples 0.980 (0.01) 0.76 (0.74-0.78) 1.00 (1.00-1.00)
All samples (nasal swab) 0.987 (0.01) 0.72 (0.69-0.75) 1.00 (1.00-1.00)
Symptomatic patients 0.981 (0.02) 0.81 (0.77-0.83) 0.99 (0.99-0.99)
Symptomatic patients (nasal swab) 0.963 (0.05) 0.80 (0.77-0.93) 0.99 (0.99-1.00)
Asymptomatic patients 0.931 (0.01) 0.55 (0.46-0.61) 1.00 (1.00-1.00)
Asymptomatic patients (nasal swab) 0.888 (0.07) 0.45 (0.37-0.52) 1.00 (1.00-1.00)
Mixed cohorts 0.960 (0.03) 0.77 (0.75-0.80) 0.99 (0.99-1.00)