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| dc.contributor.author | Cervero, Miguel | |
| dc.contributor.author | López-Wolf, Daniel | |
| dc.contributor.author | Casado, Guiomar | |
| dc.contributor.author | Novella-Mena, María | |
| dc.contributor.author | Ryan-Murua, Pablo | |
| dc.contributor.author | Taboada-Martínez, María Luisa | |
| dc.contributor.author | Rodríguez-Mora, Sara | |
| dc.contributor.author | Vigón, Lorena | |
| dc.contributor.author | Coiras, Mayte | |
| dc.contributor.author | Torres, Montserrat | |
| dc.date.accessioned | 2025-11-18T12:48:14Z | |
| dc.date.available | 2025-11-18T12:48:14Z | |
| dc.date.created | 2022 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12080/50966 | |
| dc.description.abstract | There is now sufficient evidence to support that vitamin D deficiency may predispose to SARS-CoV-2 infection and increase COVID-19 severity and mortality. It has been suggested that vitamin D3 supplementation may be used prophylactically as an affordable and safe strategy that could be added to the existing COVID-19 standard treatment. This multicenter, single-blinded, prospective randomized pilot clinical trial aimed to evaluate the safety, tolerability, and effectiveness of 10,000 IU/day in comparison with 2000 IU/day of cholecalciferol supplementation for 14 days to reduce the duration and severity of COVID-19 in 85 hospitalized individuals. The median age of the participants was 65 years (Interquartile range (IQR): 53¿74), most of them (71%) were men and the mean baseline of 25-hydroxyvitamin D (25(OH)D) in serum was 15 ng/ml (standard deviation (SD):6). After 14 days of supplementation, serum 25(OH)D levels were significantly increased in the group who received 10,000IU/day (p < 0.0001) (n = 44) in comparison with the 2,000IU/day group (n = 41), especially in overweight and obese participants, and the higher dose was well tolerated. A fraction of the individuals in our cohort (10/85) developed acute respiratory distress syndrome (ARDS). The median length of hospital stay in these patients with ARDS was significantly different in the participants assigned to the 10,000IU/day group (n = 4; 7 days; IQR: 4¿13) and the 2,000IU/day group (n = 6; 27 days; IQR: 12¿45) (p = 0.04). Moreover, the inspired oxygen fraction was reduced 7.6-fold in the high dose group (p = 0.049). In terms of blood parameters, we did not identify overall significant improvements, although the platelet count showed a modest but significant difference in those patients who were supplemented with the higher dose (p = 0.0492). In conclusion, the administration of 10,000IU/day of vitamin D3 for 14 days in association with the standard clinical care during hospitalization for COVID-19 was safe, tolerable, and beneficial, thereby helping to improve the prognosis during the recovery process. | es_ES |
| dc.format | application/pdf | es_ES |
| dc.language | eng | es_ES |
| dc.publisher | Frontiers | es_ES |
| dc.rights | CC-BY | es_ES |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/deed.es | es_ES |
| dc.source | Frontiers in Pharmacology | es_ES |
| dc.title | Beneficial Effect of Short-Term Supplementation of High Dose of Vitamin D3 in Hospitalized Patients With COVID-19: A Multicenter, Single-Blinded, Prospective Randomized Pilot Clinical Trial | es_ES |
| dc.type | Artículo | es_ES |
| dc.description.curso | 2022 | es_ES |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess | es_ES |
| dc.identifier.dl | 2022 | |
| dc.identifier.location | N/A | es_ES |