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. 2021 May 22;20:38. doi: 10.1186/s12941-021-00443-w

Table 2.

Performance characteristics of six nucleic acid amplification kits for the detection of SARS-CoV-2 using clinical diagnostic reports as the reference standard

No. of RT-qPCR result No. of clinical diagnostic report Sensitivity Specificity PPV NPV Diagnostic accuracy Kappa
Positive Negative (95% CI) (95% CI) (95% CI) (95% CI) (95% CI)
A Positive 26 0 100 (87.1–100) 100 (87.1–100) 100 (87.1–100) 100 (87.1–100) 100 1
Negative 0 26 (93.1–100) (p < 0.001)
B Positive 23 0 100 (85.7–100) 89.7 (73.6–96.4) 88.5 (71.0–96.0) 100 (87.1–100) 94.2 0.885
Negative 3 26 (84.4–98.0) (p < 0.001)
C Positive 25 0 100 (86.7–100) 96.3 (81.7–99.3) 96.2 (81.1–99.3) 100 (87.1–100) 98.1 0.962
Negative 1 26 (89.9–99.7) (p < 0.001)
D Positive 18 0 100 (82.4–100) 76.5 (60.0–87.6) 69.2 (50.0–83.5) 100 (87.1–100) 84.6 0.692
Negative 8 26 (72.5–92.0) (p < 0.001)
E Positive 20 0 100 (83.9–100) 81.3 (64.7–91.1) 76.9 (57.6–89.0) 100 (87.1–100) 88.5 0.769
Negative 6 26 (77.0–94.6) (p < 0.001)
F Positive 24 0 100 (86.2–100) 92.9 (77.4–98.0) 92.3 (75.9–97.9) 100 (87.1–100) 96.15 0.923
Negative 2 26 (87.0–98.9) (p < 0.001)