4.7 Article

Effect of arachidonic and docosahexaenoic acid supplementation on respiratory outcomes and neonatal morbidities in preterm infants

期刊

CLINICAL NUTRITION
卷 42, 期 1, 页码 22-28

出版社

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.clnu.2022.11.012

关键词

Preterm; Fatty acid supplementation; Arachidonic acid; Docosahexaenoic acid; Bronchopulmonary dysplasia; Neonatal morbidities

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This study aimed to investigate the effect of supplementation with arachidonic acid (ARA) and docosahexaenoic acid (DHA) on respiratory outcomes and neonatal morbidities in preterm infants. The results showed that supplementation with ARA and DHA significantly reduced the duration of respiratory support and oxygen demand compared to the control group, without clinically important differences in the incidence of morbidities.
Background & aims: Studies have suggested that supplementation with docosahexaenoic acid (DHA) to preterm infants might be associated with an increased risk of bronchopulmonary dysplasia (BPD). Our aim was to investigate the effect of enteral supplementation with arachidonic acid (ARA) and DHA on short-term respiratory outcomes and neonatal morbidities in very preterm infants. Methods: This is a secondary analysis of data from the ImNuT (Immature, Nutrition Therapy) study, a randomized double blind clinical trial. Infants with gestational age less than 29 weeks were randomized to receive a daily enteral supplement with ARA 100 mg/kg and DHA 50 mg/kg (intervention) or medium chain triglycerides (MCT) oil (control), from second day of life to 36 weeks postmenstrual age. Study outcomes included duration of respiratory support, incidence of BPD and other major morbidities associated with preterm birth. Results: 120 infants with mean (SD) gestational age 26.4 (1.7) weeks were randomized and allocated to either the intervention or control group. Supplementation with ARA and DHA led to a significant reduction in number of days with respiratory support (mean (95% CI) 63.4 (56.6-71.3) vs 80.6 (72.4 -88.8); p = 0.03) and a lower oxygen demand (FiO2) (mean (95% CI) 0.26 (0.25-0.28) vs 0.29 (0.27 -0.30); p = 0.03) compared to control treatment. There were no clinically important differences in incidence of BPD and other major morbidities between the treatment groups. Conclusions: Supplementation with ARA and DHA to preterm infants was safe and might have a beneficial effect on respiratory outcomes. Clinical trial registration: The trial has been registered in www.clinicaltrials.gov, ID: NCT03555019. (c) 2022 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

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