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Calcifediol treatment and COVID-19-related outcomes

Abstract:

Context

COVID-19 is a major health problem because of saturation of intensive care units (ICU) and mortality. Vitamin D has emerged as a potential treatment able to reduce the disease severity.

Objective

To elucidate the effect of calcifediol [25OHD3] treatment on COVID-19-related outcomes.

Design

Observational cohort study from March to May, 2020.

Setting

Patients admitted to COVID-19 wards of Hospital del Mar, Barcelona, Spain.

Patients

A total of 930 patients with COVID-19 were included. Ninety-two were excluded due to previous calcifediol intake.

Intervention

Of the remaining 838, a total of 447 received calcifediol (532ug on day one plus 266ug on day 3, 7, 15, and 30) whereas 391 were not treated at the time of hospital admission (Intention-to-Treat). Of the latter, 53 patients were treated later during ICU admission and were allocated in the treated group in a second analysis. In healthy subjects, calcifediol is about 3.2-fold more potent on a weight basis than cholecalciferol.

Main Outcome Measures

ICU admission and mortality.

Results

ICU assistance was required by 102 (12.2%) participants. Out of 447 patients treated with calcifediol at admission, 20 (4.5%) required ICU, compared to 82 (21%) out of 391 non-treated (p-value<0.0001). Logistic regression of calcifediol treatment on ICU admission, adjusted by age, gender, linearized 25OHD levels at baseline, and comorbidities showed that treated patients had a reduced risk to require ICU (OR 0.13 [95% CI 0.07;0.23]). Overall mortality was 10%. In the Intention-to-Treat analysis, 21 (4.7%) out of 447 patients treated with calcifediol at admission died compared to 62 patients (15.9%) out of 391 non-treated (p=0.0001). Adjusted results showed a reduced mortality risk with an OR 0.21 [95% CI 0.10; 0.43]). In the second analysis, the obtained OR was 0.52 [95% CI 0.27;0.99].

Conclusions

In patients hospitalized with COVID-19, calcifediol treatment significantly reduced ICU admission and mortality.
Publication status:
Published
Peer review status:
Peer reviewed

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Files:
Publisher copy:
10.1210/clinem/dgab405

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Role:
Author
More by this author
Role:
Author
ORCID:
0000-0002-6446-3763


Publisher:
Oxford University Press
Journal:
Journal of Clinical Endocrinology and Metabolism More from this journal
Volume:
106
Issue:
10
Pages:
e4017–e4027
Publication date:
2021-06-07
Acceptance date:
2021-06-02
DOI:
EISSN:
1945-7197
ISSN:
0021-972X


Language:
English
Keywords:
Pubs id:
1185331
Local pid:
pubs:1185331
Deposit date:
2021-07-07
ARK identifier:

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