Effect of human milk-based fortification in extremely preterm infants fed exclusively with breast milk: a randomised controlled trial
- PMID: 38545091
- PMCID: PMC10965410
- DOI: 10.1016/j.eclinm.2023.102375
Effect of human milk-based fortification in extremely preterm infants fed exclusively with breast milk: a randomised controlled trial
Erratum in
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Corrigendum to effect of human milk-based fortification in extremely preterm infants fed exclusively with breast milk: a randomised controlled trial.EClinicalMedicine. 2025 Jun 7;84:103301. doi: 10.1016/j.eclinm.2025.103301. eCollection 2025 Jun. EClinicalMedicine. 2025. PMID: 40535001 Free PMC article.
Abstract
Background: Mortality and severe morbidity remain high in extremely preterm infants. Human milk-based nutrient fortifiers may prevent serious complications and death. We aimed to investigate whether supplementation with human milk-based fortifier (HMBF), as compared to bovine milk-based fortifier (BMBF), reduced the incidence of the composite outcome of necrotising enterocolitis (NEC), sepsis, and mortality in extremely preterm infants exclusively fed human milk.
Methods: In this multicentre, randomised controlled trial at 24 neonatal units in Sweden, extremely preterm infants born between gestational week 22 + 0 and 27 + 6 fed exclusively human breast milk (mother's own and/or donor milk), were randomly assigned (1:1) to receive targeted fortification with either HMBF or BMBF. Randomisation was conducted before the enteral feeds reached 100 mL/kg/day, and was stratified by enrolment site, gestational age, singleton/twin, and sex. The allocation was concealed before inclusion, but after randomisation the study was not blinded for the clinical staff. For the NEC diagnosis, the study group was masked to an independent radiologist, and the final assessment of NEC and culture-proven sepsis was done by a blinded consensus panel review. The primary outcome was the composite of NEC stage II-III, culture-proven sepsis, and mortality from inclusion to discharge, no longer than postmenstrual week 44 + 0, in the intention-to-treat population (ClinicalTrials.gov, NCT03797157).
Findings: Between February 21st, 2019, and May 21st, 2021, 229 neonates were randomly assigned (115 HMBF, 114 BMBF). After exclusion of one infant due to parents' withdrawal of consent, 228 infants were included in the intention-to-treat analysis. Of the 115 infants assigned to HMBF, 41 (35.7%) fulfilled the criteria of either NEC, sepsis, or death, compared with 39 (34.5%) of 113 infants assigned to BMBF (OR 1.05, 95% CI 0.61-1.81, p = 0.86). Adverse events did not differ significantly between groups.
Interpretation: Supplementation with HMBF, as compared with BMBF, did not reduce the incidence of the composite outcome of NEC, sepsis, or death. Our results do not support routine supplementation with HMBF as a nutritional strategy to prevent NEC, sepsis, or death in extremely preterm infants exclusively fed human milk.
Funding: ALF grant, Prolacta Bioscience, Swedish Research Council, and Research Council for Southeast Sweden.
Keywords: Breast milk; Necrotising enterocolitis; Nutrient fortifier; Nutrition; Preterm infant; Sepsis.
© 2023 The Author(s).
Conflict of interest statement
TA received a grant for the present study by Prolacta Bioscience, CA, USA. All other authors declare no competing interests. None of the investigators have any financial interest in Prolacta Bioscience.
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References
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- Lin P.W., Stoll B.J. Necrotising enterocolitis. Lancet. 2006;368(9543):1271–1283. - PubMed
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