dc.creator | Masoli, Daniela | |
dc.creator | Mena, Patricia | |
dc.creator | Dominguez, Angelica | |
dc.creator | Ramolfo, Pamela | |
dc.creator | Vernal, Patricia | |
dc.creator | Pantoja, Miguel Angel | |
dc.creator | Esparza, Ruth | |
dc.creator | Hübner, ME | |
dc.creator | Ríos, Antonio | |
dc.creator | Faunes, Miriam | |
dc.creator | Uauy, Ricardo | |
dc.creator | Tapia, Jose L. | |
dc.date.accessioned | 2023-07-07T15:37:00Z | |
dc.date.accessioned | 2023-08-30T16:07:15Z | |
dc.date.available | 2023-07-07T15:37:00Z | |
dc.date.available | 2023-08-30T16:07:15Z | |
dc.date.created | 2023-07-07T15:37:00Z | |
dc.identifier | Journal of Pediatric Gastroenterology and Nutrition 74(3):p 424-430, March 2022. | |
dc.identifier | https://doi.org/10.1097/MPG.0000000000003321 | |
dc.identifier | https://repositorio.udd.cl/handle/11447/7651 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/8528489 | |
dc.description.abstract | Objectives: To evaluate growth (weight, length, head circumference, and knee–heel length [KHL]) in very low birth weight (VLBW) infants (500–1500 g) who received human milk with a liquid fortifier (LHMF) with high protein and fatty acid content versus a traditional powder fortifier (PHMF) for 45 days or until discharge.
Methods: This was a multicenter, randomized, controlled trial. An intention-to-treat analysis was performed to determine adverse events and withdrawal causes. We also performed an efficacy analysis involving the infants who completed at least 2 weeks of study.
Results: Of the 158 infants enrolled in the study, 146 completed at least 2 weeks, and 125 completed the entire study. The biodemographic characteristics were similar between groups, with no differences in increments of weight (22.9 vs 22.7 g kg1 day1 ), length (1.03 vs 1.09 cm/week), head circumference (0.91 vs 0.90 cm/week), or KHL (3.6 vs 3.3 mm/week). The KHL increment was greater in infants weighing >1 kg receiving LHMF (3.7 vs 3.2 mm/week, P ¼ 0.027). Although there
were no significant differences in serious adverse events, the incidence difference of the composite outcome death/necrotizing enterocolitis between groups warrants attention (1.3% with LHMF and 8.1% with PHMF).
Conclusion: There were no differences in the overall growth between VLBW infants receiving either fortifier. | |
dc.language | en | |
dc.subject | Human milk fortifiers | |
dc.subject | Neonatal nutrition | |
dc.subject | Randomized controlled trial | |
dc.subject | Very low birthweight infants | |
dc.title | Growth of Very Low Birth Weight Infants Who Received a Liquid Human Milk Fortifier: A Randomized, Controlled Multicenter Trial | |
dc.type | Article | |