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Enteral Vitamin A for Reducing Severity of Bronchopulmonary Dysplasia: A Randomized Trial
Abhijeet A Rakshasbhuvankar1,2,3,4, Karen Simmer5,2,3, Sanjay K Patole5,2,3
1Neonatal Clinical Care Unit and abhijeet.rakshasbhuvankar@health.wa.gov.au.
Insights
Enteral vitamin A supplementation in preterm infants did not reduce bronchopulmonary dysplasia (BPD) severity. While it increased plasma retinol levels, it did not impact BPD diagnosis or other clinical outcomes.
Area of Science:
- Neonatology
- Pediatric Pulmonology
- Nutritional Science
Background:
- Bronchopulmonary dysplasia (BPD) is a significant risk for preterm infants.
- Intramuscular vitamin A has shown promise in reducing BPD risk.
- The efficacy of enteral vitamin A supplementation for BPD severity is not well-established.
Purpose of the Study:
- To compare the effectiveness of enteral water-soluble vitamin A versus placebo in reducing BPD severity in extremely preterm infants.
Main Methods:
- A double-blind, randomized controlled trial was conducted.
- Infants <28 weeks gestation received either enteral vitamin A (5000 IU/day) or placebo.
- Supplementation continued until 34 weeks postmenstrual age, with BPD severity assessed via pulse oximetry.
Main Results:
- 188 infants were randomized with comparable birth weights and gestations.
- No significant difference in BPD severity was observed between vitamin A and placebo groups (P = .73).
- Enteral vitamin A did not affect BPD diagnosis or other clinical outcomes, but increased plasma retinol levels.
Conclusions:
- Enteral water-soluble vitamin A supplementation effectively increases plasma retinol levels in extremely preterm infants.
- This supplementation does not reduce the severity of bronchopulmonary dysplasia.
- Further research may be needed to explore alternative vitamin A delivery methods or dosages.
Background And Objectives:
Evidence suggests that intramuscular vitamin A reduces the risk of bronchopulmonary dysplasia (BPD) in preterm infants. Our objective was to compare enteral water-soluble vitamin A with placebo supplementation to reduce the severity of BPD in extremely preterm infants.
Methods:
We conducted a double-blind randomized controlled trial in infants <28 weeks' gestation who were to receive either enteral water-soluble vitamin A (5000 IU per day) or a placebo. Supplementation was started within 24 hours of introduction of feeds and continued until 34 weeks' postmenstrual age (PMA). The primary outcome was the severity of BPD, assessed by using the right shift of the pulse oximeter saturation versus the inspired oxygen pressure curve.
Results:
A total of 188 infants were randomly assigned. The mean ± SD birth weight (852 ± 201 vs 852 ± 211 g) and gestation (25.8 ± 1.49 vs 26.0 ± 1.39 weeks) were comparable between the vitamin A and placebo groups. There was no difference in the right shift (median [25th-75th percentiles]) of the pulse oximeter saturation versus inspired oxygen pressure curve (in kilopascals) between the vitamin A (11.1 [9.5-13.7]) and placebo groups (10.7 [9.5-13.1]) (P = .73). Enteral vitamin A did not affect diagnosis of BPD or other clinical outcomes. Plasma retinol levels were significantly higher in the vitamin A group versus the placebo group on day 28 and at 34 weeks' PMA.
Conclusions:
Enteral water-soluble vitamin A supplementation improves plasma retinol levels in extremely preterm infants but does not reduce the severity of BPD.
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