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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

From: Comparative evaluation of six nucleic acid amplification kits for SARS-CoV-2 RNA detection

 

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)