High dose vitamin D administration in ventilated intensive care unit patients: A pilot double blind randomized controlled trial

被引:126
作者
Han, Jenny E. [1 ,2 ]
Jones, Jennifer L. [3 ]
Tangpricha, Vin [3 ,4 ]
Brown, Mona A. [1 ]
Hao, Li [3 ]
Hebbar, Gautam [3 ]
Lee, Moon Jeong [3 ]
Liu, Shuling [5 ]
Brown, Lou Ann S. [6 ]
Ziegler, Thomas R. [3 ]
Martin, Greg S. [1 ,2 ]
机构
[1] Emory Univ, Dept Med, Div Pulm Allergy Crit Care & Sleep Med, Atlanta, GA 30322 USA
[2] Emory Univ, Emory Crit Care Ctr, Atlanta, GA 30322 USA
[3] Emory Univ, Dept Med, Div Endocrinol Metab & Lipids, Atlanta, GA 30322 USA
[4] Atlanta VA Med Ctr, Decatur, GA USA
[5] Emory Univ, Rollins Sch Publ Hlth, Atlanta, GA 30322 USA
[6] Emory Univ, Dept Pediat, Div Neonatal Perinatal Med, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
Vitamin D; Lung failure; Critical care; LL-37; Antimicrobial peptides;
D O I
10.1016/j.jcte.2016.04.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: There is a high prevalence of vitamin D deficiency in the critically ill patient population. Several intensive care unit studies have demonstrated an association between vitamin D deficiency [25hydroxyvitamin D (25(OH) D) < 20 ng/mL] and increased hospital length of stay (LOS), readmission rate, sepsis and mortality. Material and Methods: Pilot, double blind randomized control trial conducted on mechanically ventilated adult ICU patients. Subjects were administered either placebo, 50,000 IU vitamin D-3 or 100,000 IU vitamin D-3 daily for 5 consecutive days enterally (total vitamin D-3 dose = 250,000 IU or 500,000 IU, respectively). The primary outcome was plasma 25(OH) D concentration 7 days after oral administration of study drug. Secondary outcomes were plasma levels of the antimicrobial peptide cathelicidin (LL37), hospital LOS, SOFA score, duration of mechanical ventilation, hospital mortality, mortality at 12 weeks, and hospital acquired infection. Results: A total of 31 subjects were enrolled with 13 (43%) being vitamin D deficient at entry (25(OH) D levels < 20 ng/mL). The 250,000 IU and 500,000 IU vitamin D-3 regimens each resulted in a significant increase in mean plasma 25(OH) D concentrations from baseline to day 7; values rose to 45.7 +/- 19.6 ng/mL and 55.2 +/- 14.4 ng/mL, respectively, compared to essentially no change in the placebo group (21 +/- 11.2 ng/mL), p < 0.001. There was a significant decrease in hospital length of stay over time in the 250,000 IU and the 500,000 IU vitamin D-3 group, compared to the placebo group (25 +/- 14 and 18 +/- 11 days compared to 36 +/- 19 days, respectively; p = 0.03). There was no statically significant change in plasma LL-37 concentrations or other clinical outcomes by group over time. Conclusions: In this pilot study, high-dose vitamin D-3 safely increased plasma 25(OH) D concentrations into the sufficient range and was associated with decreased hospital length of stay without altering other clinical outcomes. (C) 2016 The Author( s). Published by Elsevier Inc.
引用
收藏
页码:59 / 65
页数:7
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