Shielding Parenteral Nutrition Solutions From Light |
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Authors: | Sophie Laborie MD Angélique Denis MS Gilles Dassieu MD Antoine Bedu MD Pierre Tourneux MD Didier Pinquier MD Elsa Kermorvant PhD MD Véronique Millet MD Serge Klosowski MD Hugues Patural MD PhD Catherine Clamadieu MD Anne Brunhes MD Marie Walther MD Isabelle Jaisson‐Hot MD Bruno Mandy Olivier Claris |
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Affiliation: | 1. Hospices Civils de Lyon, H?pital Femme Mère Enfant, Bron, France;2. Hospices Civils de Lyon‐Centre Hospitalier Lyon Sud, Pierre‐Bénite, France;3. Hospices Civils de Lyon, Lyon, France;4. Centre Hospitalier Intercommunal de Créteil, Créteil, France;5. Centre Hospitalier Universitaire de Limoges, Limoges, France;6. Centre Hospitalier Universitaire, Amiens, France;7. Centre Hospitalier Universitaire–H?pital Charles‐Nicolle, Rouen, France;8. Assistance Publique/H?pitaux de Paris‐H?pital Necker‐Enfants Malades, Paris, France;9. Université Paris Descartes, Paris, France;10. Assistance Publique–H?pitaux de Marseille–H?pital de la Conception, Marseille, France;11. Centre Hospitalier de Lens, Lens, France;12. Centre Hospitalier Universitaire de Saint Etienne, Saint Etienne, France;13. H?pital de la C?te Basque, Bayonne, France;14. Centre Hospitalier de Chambéry, Chambéry, France;15. Hospices Civils de Lyon, H?pital René Sabran, Giens, France;16. Université Claude Bernard Lyon 1, Lyon, France |
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Abstract: | Introduction: Oxidant stress is implicated in the pathogenesis of bronchopulmonary dysplasia (BPD). Light induces peroxide generation in parenteral nutrition (PN) solutions, creating an oxidant stress. Shielding PN from light decreases its peroxide content, which has nutrition and biochemical benefits in animals and humans. This study aims at determining whether full light protection of PN decreases the rate of bronchopulmonary dysplasia and/or death in very low‐birth‐weight infants. Methods: Multicenter randomized controlled trial of photoprotection, using amber bags and tubing initiated during compounding of PN and maintained throughout infusion in the light‐protected (LP) group. The control group (light exposed [LE]) received PN exposed to ambient light. Depending on centers, lipids were infused either separately or as all‐in‐one PN. Results: In total, 590 infants born <30 weeks gestational age were included. At randomization, LE and LP groups did not differ clinically except for maximal FiO2 before 12 hours. The rate of BPD/death was not different between groups at 28 days (77% LP vs 72% LE, P = .16) or at 36 weeks corrected age (30% LP vs 27% LE, P = .55). Multivariate analysis showed no significant effect of photoprotection on BPD and/or death. The rate of BPD/death was significantly lower (odds ratio, 0.54; 95% confidence interval, 0.32–0.93; P = .02) in infants receiving all‐in‐one PN vs those who received lipids separately. Conclusion: This study did not show significant beneficial effects of photoprotection. Since the decreased rate of BPD/death found with all‐in‐one PN relates to a center‐dependent variable, this warrants further investigation. |
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Keywords: | parenteral nutrition very low birth weight bronchopulmonary dysplasia peroxides preterm infant |
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