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Table 2 Comparison of C. psittaci LAMP assays using rapidly processed swab samples

From: Real-time fluorometric and end-point colorimetric isothermal assays for detection of equine pathogens C. psittaci and equine herpes virus 1: validation, comparison and application at the point of care

C. psittaci cLAMP#

C. psittaci rtLAMP

 

Positive

Negative

Total

Positive

6

2

8

Negative

0

26

26

Total

6

28

34

Kappa (0.95 CI; p(Kappa))

0.821 (0.584–1.06; 0.00)

McNemar’s Chi square (p(Chi sq))

0.500 (0.479)

Overall agreement b

94.12% (85.71% PA; 96.30% NA)

C. psittaci sgLAMP

C. psittaci rtLAMP

 

Positive

Negative

Total

Positive

6

1

7

Negative

0

29

29

Total

6

30

36

Kappa (0.95 CI; p(Kappa))

0.906 (0.726–1.09; 0.00)

McNemar’s Chi square (p(Chi sq))

0.000 (1.00)

Overall agreement b

97.22% (92.31% PA; 98.31% NA)

C. psittaci sgLAMP

C. psittaci cLAMP#

 

Positive

Negative

Total

Positive

6

1

7

Negative

2

25

27

Total

8

26

34

Kappa (0.95 CI; p(Kappa))

0.744 (0.471–1.017; 0.00)

McNemar’s Chi square (p(Chi sq))

0.000 (1.00)

Overall agreement b

91.18% (80.00% PA; 94.34% NA)

  1. #: two samples were excluded from analyses as immediate discoloration of the mix (to yellow and/or orange) was observed upon addition the swab suspension; b: positive agreement (PA) and negative agreement (NA) are outlined in brackets