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Table 3 Diagnostic performance of mNGS, GMS staining, serum LDH and BDG for PCP

From: Metagenomic next-generation sequencing for the diagnosis of Pneumocystis jirovecii Pneumonia in critically pediatric patients

Methods

PC group

Non-PCP group

Sensitivity

Specificity

PPV

NPV

mNGS

 + 

17

2

100.0%

96.7%

89.5%

100.0%

 − 

0

58

(77.1–100.0)

(87.5–99.4)

(65.5–98.2)

(92.3–100.0)

Serum BDG

 + 

13

13

86.7%

56.7%

50.0%

89.5%

 − 

2

17

(58.4–97.7)

(37.7–74.0)

(30.4–69.6)

(65.5–98.2)

GMS

 + 

1

0

5.9%

100.0%

100.0%

11.1%

 − 

16

2

(0.3–30.8)

(19.8–100)

(5.5–100)

(1.9–36.1)

LDH [30]

  ≥ 618 U/L

10

16

55.6%

71.4%

38.5%

83.3%

  < 618 U/L

8

40

(31.4–77.6)

(57.6–82.3)

(20.9–59.3)

(69.2–92.0)

  1. GMS staining gomori methenamine silver staining, serum BDG serum (1,3)-β-D-glucan, LDH lactate dehydrogenase, serum BDG < 80 ng/L was defifined as positive, LDH < 618 U/Lwas defifined as positive, CI confifidence intervals, PPV positive predict value, NPV negative predict value