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Table 2 Results of subgroup analysis based on different standards

From: The clinical efficacy of intravenous IgM-enriched immunoglobulin (pentaglobin) in sepsis or septic shock: a meta-analysis with trial sequential analysis

 

K

N

RR [95% CI]

P

Study heterogeneity

P (between-group comparison)

 

Chi2

df

I2 (%)

P

Duration of treatment

 

0.40

  ≤ 3 days

14

1027

0.58 [0.48, 0.69]

< 0.001

13.75

13

5

0.39

 

  > 3 days

3

453

0.66 [0.47, 0.81]

< 0.001

2.33

3

0

0.51

Daily dose

 

0.14

 Low (≤ 0.25 g/kg)

10

685

0.52 [0.42, 0.65]

< 0.001

5.12

9

0

0.82

 

 High (> 0.25 g/kg)

5

606

0.68 [0.55, 0.85]

< 0.001

7.06

4

29

0.22

Total dose

 

0.03

 Low (< 0.9 g/kg)

11

740

0.50 [0.40, 0.62]

< 0.001

7.39

10

0

0.69

 

 High (≥ 0.9 g/kg)

5

551

0.70 [0.56, 0.87]

0.002

3.80

4

0

0.43

Type of control intervention

 

0.14

  Placebo

14

1141

0.57 [0.48, 0.67]

< 0.001

11.26

13

0

0.59

 

Human albumin solution

5

389

0.74 [0.54, 1.01]

0.05

1.56

4

0

0.45

Follow-up duration

 

0.21

  ≤ 28 days

11

1135

0.64 [0.54, 0.76]

< 0.001

10.14

10

1

0.43

 

  > 28 days

3

158

0.35 [0.17, 0.71]

0.004

3.42

2

42

0.18

 ICU days

5

237

0.56 [0.40, 0.77]

< 0.001

1.87

4

0

0.76

Study design

 

0.27

 Randomized controlled trial

15

978

0.65 [0.53, 0.78]

< 0.001

10.72

14

0

0.71

 

Cohort study

4

552

0.35 [0.25, 0.50]

< 0.001

4.80

3

37

0.19

Publication year

        

0.21

 Old studies (before 2005)

10

485

0.52 [0.40, 0.68]

< 0.001

6.38

9

0

0.70

 

 Recent studies (from 2005)

9

1045

0.64 [0.54, 0.76]

< 0.001

10.05

8

20

0.26

  1. K number of studies, N number of participants, ICU intensive care unit, RR relative risk, CI confidence interval