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. 2021 Oct 27;28(1):78–81. doi: 10.1016/j.jiac.2021.10.024

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.