Skip to main content

Table 1 Comparison of phenotypic and molecular assays apllied to bloodculture bottles

From: Diagnosis of bacteremia in pediatric oncologic patients by in-house real-time PCR

 

Phenotipyc detection and identification by phenotypic analisys (n = 124)

Molecucar detection by GP/GN multiplex PCR

Concordance (%)

Molecular identification by specific-species qPCR (n = 124)

Concordance (%)

Average Cycle threshold

S. aureus

12

12

100 %

10

83.40 %

17,683

SCoN

35

28

80 %

32

91.40 %

20,608

Enterococcus spp.

5

5

100 %

5

100 %

24,923

S. pneumoniae

1

1

100 %

1

100 %

20,977

K. pneumoniae

3

3

100 %

3

100 %

29,111

E. cloacae

6

6

100 %

6

100 %

20,919

E. coli

8

7

87.50 %

7

87.50 %

18,995

S. marcescens

2

2

100 %

2

100 %

25,252

P. aeruginosa

14

13

92.80 %

13

92.80 %

19,395

S. malthofilia

1

1

100 %

1

100 %

36,974

Acinetobacter spp.

1

1

100 %

1

100 %

27,993

Candida spp.

12

12

100 %

3

25 %

25,464

Other fungi

2

2

100 %

a

a

a

Streptococcus sp.

9

7

77.80 %

a

a

a

Others

13

12

92.30 %

a

a

a

  1. aSpecies not included in the in-house qPCR standardized assay described in this study