Effect of adjunctive single high-dose vitamin D3 on outcome of community-acquired pneumonia in hospitalised adults: The VIDCAPS randomised controlled trial
2018; Nature Portfolio; Volume: 8; Issue: 1 Linguagem: Inglês
10.1038/s41598-018-32162-2
ISSN2045-2322
AutoresSandy Slow, Michael Epton, Malina Storer, Rennae Thiessen, Steven Lim, James Wong, Paul K. L. Chin, Pleayo Tovaranonte, John Pearson, Stephen T. Chambers, David R. Murdoch, David L. Jardine, Alan Pithie, Christopher Warren, Suzanne Faville, Avinesh Shankar, Evan Wm. Cameron, Tom Evans, Pamela KL Mooi, C. H. McDonald, Huan Chan, J. Llewelyn, Michael Liu,
Tópico(s)Pharmacological Effects and Toxicity Studies
ResumoLow vitamin D status is associated with increased risk of pneumonia, greater disease severity and poorer outcome. However, no trials have examined the effect of adjunctive vitamin D therapy on outcomes in adults with community-acquired pneumonia (CAP). We conducted a randomised, double-blind, placebo-controlled trial examining the effects of adjunctive vitamin D in adults hospitalised with CAP. Participants were randomised to either a single oral dose of 200,000 IU vitamin D3 or placebo. The primary outcome was the complete resolution of chest radiograph infiltrate at 6 weeks post-study treatment. Secondary outcomes included length of hospital stay, intensive care admission and return to normal activity. Only participants who completed the study or died within the 6 week period were included in the analysis (n = 60 vitamin D, n = 57 placebo). Adjunctive vitamin D did not have any effect on the primary outcome (OR 0.78, 95% CI 0.31 to 1.86, p = 0.548). However, there was evidence it increased the complete resolution of pneumonia in participants with baseline vitamin D levels <25 nmol/L (OR 17.0, 95% CI 1.40-549.45, P = 0.043), but this did not reach statistical significance using exact methods (OR 13.0, 95%CI 0.7-960.4, P = 0.083). There were no significant effects for any secondary outcome.
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