Hypercalcemia Without Hypervitaminosis D During Cholecalciferol Supplementation in Critically Ill Patients
Background Vitamin D deficiency during critical illness has been associated with worsened outcomes. Because most critically ill patients with severe traumatic injuries are vitamin D deficient, we investigated the efficacy and safety of cholecalciferol therapy for these patients. Methods Fifty‐three...
Gespeichert in:
Veröffentlicht in: | Nutrition in clinical practice 2020-10, Vol.35 (5), p.933-941 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Background
Vitamin D deficiency during critical illness has been associated with worsened outcomes. Because most critically ill patients with severe traumatic injuries are vitamin D deficient, we investigated the efficacy and safety of cholecalciferol therapy for these patients.
Methods
Fifty‐three patients (>17 years of age) admitted to the trauma intensive care unit who had a serum 25‐hydroxy vitamin D (25‐OH vit D) concentration 1.32 mmol/L) or hypervitaminosis D (25‐OH vit D >79.9 nmol/L). Patients were monitored for 2 weeks during cholecalciferol therapy. Results: Twenty‐four patients (45%) achieved target 25‐OH vit D. No patients experienced hypervitaminosis D. Hypercalcemia occurred in 40% (n = 21) of patients; 2 patients experienced an iCa >1.49 nmol/L. 25‐OH vit D was significantly greater for those who developed hypercalcemia (37.2 + 11.2 vs 28.4 + 5.6 ng/mL, respectively, P < 0.001) by the second week of cholecalciferol. Of 24 patients who achieved target 25‐OH vit D, 14 (58%) experienced hypercalcemia in contrast to 24% of patients (7 out of 29) who did not achieve target 25‐OH vit D (P = 0.024).
Conclusions
Cholecalciferol normalized serum 25‐OH vit D concentrations in less than half of patients yet was associated with a substantial proportion of patients with hypercalcemia without hypervitaminosis D. |
---|---|
ISSN: | 0884-5336 1941-2452 |
DOI: | 10.1002/ncp.10407 |