Iron supplementation and the risk of bronchopulmonary dysplasia in extremely low gestational age newborns

San Antonio Uniformed Services Health Education Consortium, San Antonio, TX, USA. University of Washington, Seattle, WA, USA. Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA, USA. Pediatrix Medical Group, Dallas, TX, USA. Baylor University Medical Center, Dallas, TX, USA. Emory University School of Medicine and Center for Transfusion and Cellular Therapies, Atlanta, GA, USA. University of Minnesota, Minneapolis, MN, USA. San Antonio Uniformed Services Health Education Consortium, San Antonio, TX, USA. Pediatrix Medical Group, San Antonio, TX, USA. Baylor College of Medicine, San Antonio, TX, USA. Pediatrix and Obstetrix Specialists of Houston, Houston, TX, USA. Methodist Children's Hospital, San Antonio, TX, USA.

Pediatric research. 2022
BACKGROUND The aim of this study was to determine the relationship between iron exposure and the development of bronchopulmonary dysplasia (BPD). METHODS A secondary analysis of the PENUT Trial dataset was conducted. The primary outcome was BPD at 36 weeks gestational age and primary exposures of interest were cumulative iron exposures in the first 28 days and through 36 weeks' gestation. Descriptive statistics were calculated for study cohort characteristics with analysis adjusted for the factors used to stratify randomization. RESULTS Of the 941 patients, 821 (87.2%) survived to BPD evaluation at 36 weeks, with 332 (40.4%) diagnosed with BPD. The median cohort gestational age was 26 weeks and birth weight 810 g. In the first 28 days, 76% of infants received enteral iron and 55% parenteral iron. The median supplemental cumulative enteral and parenteral iron intakes at 28 days were 58.5 and 3.1 mg/kg, respectively, and through 36 weeks' 235.8 and 3.56 mg/kg, respectively. We found lower volume of red blood cell transfusions in the first 28 days after birth and higher enteral iron exposure in the first 28 days after birth to be associated with lower rates of BPD. CONCLUSIONS We find no support for an increased risk of BPD with iron supplementation. TRIAL REGISTRATION NUMBER NCT01378273. IMPACT Prior studies and biologic plausibility raise the possibility that iron administration could contribute to the pathophysiology of oxidant-induced lung injury and thus bronchopulmonary dysplasia in preterm infants. For 24-27-week premature infants, this study finds no association between total cumulative enteral iron supplementation at either 28-day or 36-week postmenstrual age and the risk for developing bronchopulmonary dysplasia.
Study details
Language : eng
Credits : Bibliographic data from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine