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Serum phosphorus levels in premature infants receiving a donor human milk derived fortifier
Katherine E Chetta1, Amy B Hair2, Keli M Hawthorne3
1USDA/ARS Children's Nutrition Research Center, Department of Pediatrics, Section of Neonatology, Baylor College of Medicine, Texas Children's Hospital, Houston, TX 77030, USA. kewiley@bcm.edu.
Insights
Premature infants receiving human milk fortified with donor human milk-derived fortifier (HMDF) may experience mild, temporary high serum phosphorus levels. This risk decreases with infant age and is not linked to birth weight or gender.
Area of Science:
- Neonatal Nutrition
- Pediatric Endocrinology
- Human Milk Fortification
Background:
- Anecdotal reports suggest elevated serum phosphorus (P) in premature infants fed donor human milk-derived fortifier (HMDF).
- Prospective studies investigating serum P levels in this specific population are lacking.
Purpose of the Study:
- To prospectively evaluate serum phosphorus levels in extremely premature infants fed an exclusive human milk-based diet with HMDF.
- To identify factors associated with serum P elevations in this cohort.
Main Methods:
- A single-center prospective observational cohort study.
- Included 93 extremely premature infants (≤ 1250g birth weight).
- Monitored serum P levels and analyzed correlations with infant characteristics and HMDF energy density.
Main Results:
- 18.3% of infants had at least one high serum P level (mean 9.2 ± 1.1 mg/dL) around 19 days of life.
- Highest serum P was inversely correlated with infant age (p < 0.001) and positively correlated with HMDF energy density (p = 0.035).
- Serum P showed no significant relationship with gender, birth weight, gestational age, or time to full feeds.
Conclusions:
- Hyperphosphatemia incidence in premature infants receiving HMDF was mild and transient.
- Risk of elevated serum P decreased with infant age.
- Serum P levels were not significantly related to infant demographics or feeding milestones.
Abstract:
An elevated serum phosphorus (P) has been anecdotally described in premature infants receiving human milk fortified with donor human milk-derived fortifier (HMDF). No studies have prospectively investigated serum P in premature infants receiving this fortification strategy. In this single center prospective observational cohort study, extremely premature infants ≤ 1250 grams (g) birth weight (BW) were fed an exclusive human milk-based diet receiving HMDF and serum P levels were obtained. We evaluated 93 infants with a mean gestational age of 27.5 ± 2.0 weeks (Mean ± SD) and BW of 904 ± 178 g. Seventeen infants (18.3%) had at least one high serum P level with a mean serum P of 9.2 ± 1.1 mg/dL occurring at 19 ± 11 days of life. For all infants, the highest serum P was inversely correlated to the day of life of the infant (p < 0.001, R2 = 0.175) and positively correlated with energy density of HMDF (p = 0.035). Serum P was not significantly related to gender, BW, gestational age, or days to full feeds. We conclude that the incidence of hyperphosphatemia was mild and transient in this population. The risk decreased with infant age and was unrelated to gender, BW, or ethnicity.
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