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Effect of a single high-dose vitamin d3 on the length of hospital stay of severely 25-hydroxyvitamin d-deficient patients with COVID-19
Murai, Igor H.; Fernandes, Alan L.; Antonangelo, Leila; Gualano, Bruno; Pereira, Rosa Maria Rodrigues.
  • Murai, Igor H.; Universidade de Sao Paulo. Faculdade de Medicina FMUSP. Divisao de Reumatologia. Sao Paulo. BR
  • Fernandes, Alan L.; Universidade de Sao Paulo. Faculdade de Medicina FMUSP. Divisao de Reumatologia. Sao Paulo. BR
  • Antonangelo, Leila; Universidade de Sao Paulo. Faculdade de Medicina. Divisao de Patologia Clinica, Hospital das Clinicas HCFMUSP. Sao Paulo. BR
  • Gualano, Bruno; Universidade de Sao Paulo. Faculdade de Medicina FMUSP. Divisao de Reumatologia. Sao Paulo. BR
  • Pereira, Rosa Maria Rodrigues; Universidade de Sao Paulo. Faculdade de Medicina FMUSP. Divisao de Reumatologia. Sao Paulo. BR
Clinics ; 76: e3549, 2021. tab, graf
Article in English | LILACS | ID: biblio-1350602
ABSTRACT

OBJECTIVES:

In this ancillary analysis of a multicenter, double-blinded, randomized, placebo-controlled trial, we investigated the effect of a single high dose of vitamin D3 on the length of hospital stay of patients with severe 25-hydroxyvitamin D deficiency and COVID-19.

METHODS:

The primary outcome was length of hospital stay, defined as the total number of days that patients remained hospitalized from the date of randomization until the date of hospital discharge. Secondary outcomes included serum levels of 25-hydroxyvitamin D, mortality during hospitalization, number of patients admitted to the intensive care unit, and number of patients who required mechanical ventilation. ClinicalTrials.gov NCT04449718.

RESULTS:

Thirty-two patients were included in the study. The mean (SD) age was 58.5 (15.6) years, body mass index was 30.8 (8.6) kg/m2, and 25-hydroxyvitamin D level was 7.8 (1.6) ng/mL. No significant difference was observed in the median interquartile range of length of hospital stay between the vitamin D3 group (6.0 [4.0-18.0] days) versus placebo (9.5 [6.3-15.5] days) (log-rank p=0.74; hazard ratio, 1.13 [95% confidence interval (CI), 0.53-2.40]; p=0.76). Vitamin D3 significantly increased serum 25-hydroxyvitamin D levels in the vitamin D3 group compared with that in the placebo group (between-group difference, 23.9 ng/mL [95% CI, 17.7-30.1]; p<0.001).

CONCLUSIONS:

A dose of 200.000 IU of vitamin D3 did not significantly reduce the length of hospital stay of patients with severe 25-hydroxyvitamin D deficiency and COVID-19.
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Vitamin D Deficiency / COVID-19 Type of study: Controlled clinical trial Limits: Humans Language: English Journal: Clinics Journal subject: Medicine Year: 2021 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade de Sao Paulo/BR

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Full text: Available Index: LILACS (Americas) Main subject: Vitamin D Deficiency / COVID-19 Type of study: Controlled clinical trial Limits: Humans Language: English Journal: Clinics Journal subject: Medicine Year: 2021 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade de Sao Paulo/BR