Effect of Early High-Dose Vitamin D3 Repletion on Cognitive Outcomes in Critically Ill Adults

Abstract

Long-term cognitive impairment frequently occurs after critical illness; no treatments are known to improve long-term cognition. Does a single high-dose (540,000 International Units) enteral treatment of vitamin D3 given shortly after hospital admission in critically ill patients who are vitamin D deficient improve long-term global cognition or executive function? This study evaluated long-term cognitive outcomes among patients enrolled in a multicenter, blinded, randomized clinical trial comparing vitamin D3 treatment vsplacebo in critically ill adults with vitamin D deficiency. Global cognition was measured by the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS). Executive function was measured with a composite score derived from three Delis-Kaplan Executive Function System subscales. Outcomes were assessed at a median of 443days (interquartile range, 390-482days) after randomization and were compared using multivariate proportional odds regression. Adjusted ORs of > 1.0 would indicate better outcomes in the vitamin D3 group compared with the placebo group. Ninety-five patients were enrolled, including 47 patients randomized to vitamin D3 treatment and 48 patients randomized to placebo. The adjusted median RBANS score at follow-up was 79.6 (95%CI, 73.0-84.0) in the vitamin D3 group and 82.1 (95%CI, 74.7-84.6) in the placebo group (adjusted OR, 0.83; 95%CI, 0.50-1.38). The adjusted median executive function composite scores were 8.1 (95%CI, 6.8-9.0) and 8.7 (95%CI, 7.4-9.3), respectively (adjusted OR, 0.72; 95%CI, 0.36-1.42). In vitamin D-deficient, critically-ill adults, a large dose of enteral vitamin D3 did not improve long-term global cognition or executive function. ClinicalTrials.gov; No.: NCT03733418; URL: www.clinicaltrials.gov.