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Table 3 Different baseline characteristics of patient responder and non-responder to vitamin D supplementation on day 3 after study drug administration. Odds ratios for 28-day mortality for vitamin D supplementation in a bivariate analysis with an interaction term for the covariates. If the interaction term was not significant, the odds ratio of treatment adjusted for covariate without interaction term was reported

From: Trying to identify who may benefit most from future vitamin D intervention trials: a post hoc analysis from the VITDAL-ICU study excluding the early deaths

 

Vitamin D supplementation group (N = 204)*

Responder (N = 133)

Non-responder (N = 71)

p value

Age, years

64 ± 16

61 ± 13

0.19

Body mass index

27.3 ± 4.7

27.2 ± 4.9

0.87

25-Hydroxyvitamin D, ng/ml

13.2 ± 4.5

12.3 ± 4.8

0.19

1,25-Dihydroxyvitamin D, pg/ml

48 (40–57)

34 (24–44)

0.05

Charlson Comorbidity Index

2.8 (2.3–3.2)

3 (2.5–3.5)

0.59

SAPS 2

33 (30–36)

29 (26–32)

0.04

TISS

36 (35–37)

41 (39–42)

< 0.01

Male/female gender, N/N

86/47

45/26

0.86

Chronic kidney disease, N (%)

35 (26.3)

18 (25.4)

0.88

Surgical/medical and neuro admission N(%)/N(%)

64 (48)/69 (52)

55 (77)/16 (33)

< 0.01

Chronic liver disease, N (%)

13 (9.8)

16 (22.5)

0.01

COPD, N (%)

27 (20.3)

10 (14)

0.27

Ischemic heart disease—chronic heart failure, N (%)

67 (50.4)

36 (50.7)

0.96

Malignant disease, N (%)

13 (9.8)

6 (8.5)

0.76

Mechanical ventilation at enrollment, N (%)

78 (58.6)

55 (77.5)

0.02

Use of vasopressor at enrollment, N (%)

57 (42.9)

47 (66.2)

< 0.01

  1. Definition of responder to vitamin D supplementation: plasma level increase of > 10 ng/ml on day 3 after study drug administration
  2. *The analysis is performed just in the treatment group since in the placebo group, there were no patients classified as responders according to our criteria