Table 1.
Sensitivity and specificity of the RapidTesta SARS-CoV-2 without the use of a digital immunoassay device among all patients in the study.
real-time RT-PCR |
|||
---|---|---|---|
Positive | Negative | ||
Antigen test | Positive | 53 | 8 |
Negative |
21 |
1045 |
|
Sensitivity (%) | 71.6(59.9–81.5) | ||
Specificity (%) | 99.2(98.5–99.7) |
Reverse transcription-polymerase chain reaction findings were used as reference results.
RT-PCR, reverse transcription-polymerase chain reaction.
Data in parentheses indicate 95% confidence intervals.