Growth of Very Low Birth Weight Infants Who Received a Liquid Human Milk Fortifier: A Randomized, Controlled Multicenter Trial
dc.catalogador | pau | |
dc.contributor.author | Masoli, Daniela | |
dc.contributor.author | Mena, Patricia | |
dc.contributor.author | Domínguez, Angélica | |
dc.contributor.author | Ramolfo, Pamela | |
dc.contributor.author | Vernal, Patricia | |
dc.contributor.author | Pantoja, Miguel Angel | |
dc.contributor.author | Esparza, Ruth | |
dc.contributor.author | Hübner, Maria Eugenia | |
dc.contributor.author | Ríos, Antonio | |
dc.contributor.author | Faunes, Miriam | |
dc.contributor.author | Uauy, Ricardo | |
dc.contributor.author | Tapia, Jose L. | |
dc.contributor.other | Neocosur Network | |
dc.date.accessioned | 2024-03-06T14:05:52Z | |
dc.date.available | 2024-03-06T14:05:52Z | |
dc.date.issued | 2022 | |
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 kg−1 day−1), 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 = 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.fechaingreso.objetodigital | 2024-11-14 | |
dc.fuente.origen | ORCID | |
dc.identifier.doi | 10.1097/mpg.0000000000003321 | |
dc.identifier.uri | http://dx.doi.org/10.1097/mpg.0000000000003321 | |
dc.identifier.uri | https://repositorio.uc.cl/handle/11534/84244 | |
dc.identifier.wosid | WOS:000761954400024 | |
dc.information.autoruc | Escuela de Medicina; Domínguez, Angélica; 0000-0001-7477-7574; 131798 | |
dc.language.iso | en | |
dc.nota.acceso | contenido parcial | |
dc.rights | acceso restringido | |
dc.subject.ods | 03 Good health and well-being | |
dc.subject.odspa | 03 Salud y bienestar | |
dc.title | Growth of Very Low Birth Weight Infants Who Received a Liquid Human Milk Fortifier: A Randomized, Controlled Multicenter Trial | |
dc.type | artículo | |
sipa.codpersvinculados | 131798 | |
sipa.trazabilidad | ORCID;2024-01-15 |
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