# Vitamin D supplementation in critically ill patients: a meta-analysis

**Authors:** Wen-He Zheng, Jia-Heng Shi, Da-Xing Yu, Hui-Bin Huang

PMC · DOI: 10.3389/fnut.2025.1505616 · Frontiers in Nutrition · 2025-04-30

## TL;DR

This study finds that vitamin D supplementation reduces short-term mortality and improves outcomes in critically ill patients, especially those needing mechanical ventilation.

## Contribution

The study provides novel evidence that vitamin D benefits critically ill patients, particularly those on mechanical ventilation.

## Key findings

- Vitamin D significantly reduced short-term mortality in critically ill patients.
- Vitamin D decreased the duration of mechanical ventilation and ICU length of stay.
- Patients on mechanical ventilation benefited more from vitamin D supplementation.

## Abstract

Vitamin D is commonly used in clinical practice, while its clinical significance in critically ill patients remains controversial. Therefore, we aimed to perform a systemic review and meta-analysis to investigate the effect of vitamin D on this patient population.

We searched for randomized controlled trials (RCTs) in PubMed, Embase, and the Cochrane Library databases from inception until August 15, 2024. Studies evaluating critically ill adult patients who received vitamin D compared to controls were included. The primary outcome was short-term mortality. We used the Cochrane risk of bias tool and GRADE system to evaluate the study quality and evidence. Secondary outcomes were changes in serum 25-hydroxyvitamin D levels, mechanical ventilation (MV) duration, and length of stay (LOS) in the ICU or hospital. We also conducted meta-regression, subgroup analyses, and trial sequential analysis (TSA) to explore the potential heterogeneity among the included trials.

Nineteen RCTs with 2,754 patients were eligible. Overall, vitamin D significantly increased serum 25-hydroxyvitamin D levels and significantly reduced the short-term mortality (risk ratio [RR] = 0.83; 95%CI, 0.70–0.98; p = 0.03, I2 = 13%), duration of MV (MD = −2.96 days; 95% CI, −5.39 to −0.52; I2 = 77%; p = 0.02) and ICU LOS (MD = −2.66 days; 95% CI, −4.04 to −1.29, I2 = 70%; p = 0.0001) but not hospital LOS (MD = −0.48 days; 95% CI, −2.37 to 1.40; I2 = 31%; p = 0.61). The meta-regression analysis revealed that the proportion of MV (MV%) accounted for the source of heterogeneity, and the subgroup analyses based on MV% suggested that the MV group was more likely to benefit from vitamin D applications than the partly MV group in all the predefined outcomes (all p values<0.05). TSA for short-term mortality suggested that more data is required to confirm our main conclusion.

Vitamin D supplementation increased serum 25-hydroxyvitamin D levels and significantly benefited critically ill patients, especially those with MV.

https://inplasy.com/inplasy-2022-10-0074/, INPLASY2022100074.

## Full-text entities

- **Diseases:** HS (MESH:C567159), sepsis (MESH:D018805), acute liver failure (MESH:D017114), respiratory insufficiency (MESH:D012131), muscle fiber atrophy (MESH:D009133), VDD (MESH:D014808), infection (MESH:D007239), adiposity (MESH:D018205), Osteoporosis (MESH:D010024), intestinal dysfunction (MESH:D007410), critically ill (MESH:D016638), COPD (MESH:D029424), ventilator-related lung injury (MESH:D055397), MV (MESH:D053717), anemia (MESH:D000740), sarcopenia (MESH:D055948)
- **Chemicals:** iron (MESH:D007501), 25-hydroxyvitamin D (MESH:C104450), Vit D (MESH:D014807), 1,25(OH)D (-), calcitriol (MESH:D002117), phosphorus (MESH:D010758), alfacalcidol (MESH:C008088), calcium (MESH:D002118)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12075268/full.md

## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12075268/full.md

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Source: https://tomesphere.com/paper/PMC12075268