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Vitamin A in Prevention of Bronchopulmonary Dysplasia
Hercília Guimarães1, Maria Beatriz Guedes, Gustavo Rocha
1Faculty of Medicine of Porto University, NICU, São João Hospital, Alameda Prof Hernâni Monteiro, 4200-319 Porto. herciliaguimaraes@gmail.com.
Insights
Vitamin A supplementation may reduce death or bronchopulmonary dysplasia (BPD) in very preterm infants. Prenatal and neonatal vitamin A may offer better prevention, but further research is needed on optimal delivery and high-dose effectiveness.
Area of Science:
- Neonatology
- Pediatric Pulmonology
- Nutritional Science
Background:
- Bronchopulmonary dysplasia (BPD) is a significant challenge for preterm infants, with lower vitamin A levels potentially impairing antioxidant defenses and lung development.
- Vitamin A is crucial for fetal lung growth, surfactant production, and immune modulation, with retinoic acid enhancing alveolar septation.
Purpose of the Study:
- To evaluate the role of vitamin A supplementation in preventing bronchopulmonary dysplasia (BPD) in very low birth weight (VLBW) infants.
- To assess the impact of vitamin A on mortality and long-term neurodevelopmental outcomes in VLBW infants.
Main Methods:
- Review of existing evidence on vitamin A supplementation (parenteral and antenatal) for BPD prevention in VLBW infants.
- Analysis of data regarding the number needed to treat for BPD reduction and neurodevelopmental outcomes.
Main Results:
- Parenteral vitamin A supplementation is a recommended preventive therapy for BPD, with a number needed to treat of 12.
- No clear benefit or harm was observed regarding long-term neurodevelopmental status or cerebral palsy.
- Antenatal vitamin A administration combined with neonatal supplementation may be more effective in preventing BPD, especially in vitamin A-deficient areas.
Conclusions:
- Vitamin A supplementation is a viable preventive strategy for BPD in VLBW infants.
- Further trials are required to evaluate intravenous vitamin A emulsions, combined prenatal/postnatal strategies, and high-dose vitamin A in extremely low birth weight (ELBW) infants.
Abstract:
Bronchopulmonary dysplasia (BPD) remains one of the most serious challenges in the care of the very preterm infants, affecting approximately one-quarter of infants born <1500g birth weight and 30% <1000g. Oxygen toxicity may contribute to its pathogenesis. Vitamin A concentrations are lower in BPD infants which may result in a reduction of the antioxidant protection. It has been found to up regulate genes necessary for fetal lung growth and increase surfactant production in animal models and is also involved in the modulation of immunological and inflammatory responses by regulation of cytokine production. Retinoic acid plays a key role in lung development improving alveolar septation. Evidence exists that vitamin A supplementation for very low birth weight (VLBW) infants, beyond that routinely given in multivitamin preparations, is associated with a reduction in death or BPD. So, parenteral administration of vitamin A to the newborn is one of the current recommended preventive therapies for BPD (number needed to treat 12; 95% CI:6-94; The information on long-term neurodevelopmental status suggests no evidence of either benefit or harm. Estimates for cerebral palsy range from a number needed to treat of 11 to a number needed to harm of 33. Nowadays, is seems that administration of antenatal vitamin A to the mother in late pregnancy associated with neonatal supplementation can better prevent the development of BPD in areas of endemic vitamin A deficiency. The benefits, in terms of vitamin A status, safety and acceptability of delivering vitamin A in an intravenous emulsion compared with repeat intramuscular injections, the association of vitamin A prenatal and postnatal, as well as the effectiveness and safety of administered high dose vitamin A in ELBW infants waits evaluation and should be assessed in further trials.
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