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Table 3 Subgroup analyses of paricalcitol compared with other VDRAs for target reduction of iPTH from baseline

From: Comparative efficacy and safety of paricalcitol versus vitamin D receptor activators for dialysis patients with secondary hyperparathyroidism: a meta-analysis of randomized controlled trials

Subgroup

No.patients

No.trials

Relative Risk(95% CI)

P Value

I2(%)

Test of Interaction, P

Total

696

5

1.01 (0.87,1.18)

0.85

31

Not applicable

Baseline iPTH level

  < 68.4 pmol/L

407

3

0.97 (0.78,1.20)

0.77

51

0.49

  > 68.4 pmol/L

289

2

1.09 (0.84,1.42)

0.51

13

 

Types of dialysis

 Hemodialysis

670

4

1.03 (0.87,1.20)

0.76

41

0.44

 Peritoneal dialysis

26

1

0.78 (0.39,1.55)

0.47

31

 

Routine of administration

 Oral

92

2

0.82 (0.61,1.11)

0.21

0

0.14

 Intravenous

604

3

1.07 (0.91,1.26)

0.42

38

 

Sample size

 Small, n < 100

178

3

0.98 (0.75,1.28)

0.87

42

0.82

 Large, n > 100

518

2

1.02 (0.79,1.32)

0.88

60

 

Risk of bias

 Low quality

92

2

0.82 (0.61,1.11)

0.21

0

0.14

 High quality

604

3

1.07 (0.91,1.26)

0.42

38

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