calciol/Finding
One finding, on its own
A single claim from the graph, with the evidence strength computed from its study, the sentence it was drawn from, and the paper. This address does not change.
No detected effect on all-cause mortality
ModerateEvidence strength: moderate. Human evidence with one recorded weakness, or capped at moderate by its design or by unread numbers.FindingNull resultreplicated ×5“And while 30-day ICU readmission rate was still higher in the placebo group compared to the cholecalciferol group (20% versus 0%; p<0.001, respectively), there was no difference between them in terms of 30-day all-cause mortality (30% versus 25%; p=0.43, respectively).”
Quoted verbatim from Effect of Cholecalciferol Supplementation on Vitamin D Status and Cathelicidin Levels in Sepsis: A Randomized, Placebo-Controlled Trial.. - Study
- RCT
- Duration
- 4 weeks
- Dose
- single bolus of 200,000 IU or 400,000 IU cholecalciferol (arms combined), versus matched placebo
- Population
- Adult ICU patients within 24 hours of new-onset severe sepsis or septic shock; post-hoc analysis combining the 200,000 IU and 400,000 IU cholecalciferol arms against placebo; 30-day horizon
Effect of Cholecalciferol Supplementation on Vitamin D Status and Cathelicidin Levels in Sepsis: A Randomized, Placebo-Controlled Trial.2015PMID:26086941Permalink
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To cite this finding: https://catalystproject.ai/e/01M5JT43NYTA2RRN41THXTZFSR