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Clinical Observation of Extensively Hydrolysis Protein Formula With Feeding Intolerance in Preterm Infants
Liping Yin1, Jingjing Ma1, Heng Liu1
1Department of Pediatrics, Zhongda Hospital Affiliated to Southeast University, Nanjing, China.
Insights
Extensively hydrolyzed protein formula (EHF) reduced feeding intolerance and necrotizing enterocolitis in preterm infants. However, EHF did not improve growth and may increase metabolic bone disease risk.
Area of Science:
- Neonatal nutrition
- Pediatric gastroenterology
Background:
- Preterm infants often face feeding challenges in the NICU.
- Breastfeeding may not always be possible for these vulnerable infants.
Purpose of the Study:
- To evaluate the benefits of extensively hydrolyzed formula (EHF) compared to standard preterm formula (SPF) for preterm infants (GA ≤34 weeks) when breastfeeding is not feasible.
Main Methods:
- A randomized controlled trial involving 370 preterm infants (GA ≤34 weeks).
- Infants were fed either EHF or SPF during NICU hospitalization.
- Outcomes including feeding intolerance, necrotizing enterocolitis, and growth were assessed during hospitalization and for 6 months post-discharge.
Main Results:
- EHF significantly reduced feeding intolerance (14.1% vs. 30.3%) and necrotizing enterocolitis (2.2% vs. 6.5%) compared to SPF.
- No significant differences were observed in growth parameters (weight, head circumference, length) during hospitalization or follow-up.
- Serum phosphorus levels decreased and alkaline phosphatase increased in the EHF group, suggesting potential bone metabolism changes.
Conclusions:
- EHF is beneficial in reducing feeding intolerance and necrotizing enterocolitis in preterm infants.
- EHF does not offer advantages in establishing enteral nutrition, reducing parenteral nutrition time, or hospitalization duration.
- EHF shows limited impact on physical growth and may be associated with an increased risk of metabolic bone disease.
Objective:
To investigate whether feeding extensively hydrolysis protein formula during the NICU hospitalization was more beneficial for preterm infants with a gestational age (GA) ≤34 weeks when breastfeeding was not possible.
Methods:
In total, 587 preterm infants were randomly divided into two groups: observation groups fed with extensively hydrolyzed formula (EHF) milk and control groups fed with standard preterm formula (SPF) milk until discharge from the neonatal intensive care unit (NICU). The incidence of complications during hospitalization was recorded in both groups. Then, two groups were uniformly fed with 0-to-6-month infant formula milk and followed-up for 6 months after discharge.
Results:
The final study included 370 premature infants, including 185 babies in the observation group and 185 in the control group. In contrast to the SPF, feeding EHF among preterm infants of GA <34 weeks during NICU hospitalization significantly reduced the incidence of feeding intolerance (FI) (14.1 vs. 30.3%, p < 0.01). The incidence of necrotizing enterocolitis (NEC) was significantly reduced in the observation group (2.2 vs. 6.5%, p < 0.05), but there was no significant difference in the incidence of other related complications. At discharge, there was no difference in total serum protein (46.6 vs. 46.4 g/L), albumin (33.5 vs. 34.2 g/L), and calcium (2.37 vs. 2.35 mmol/L), but the serum phosphorus concentrations associated with skeletal mineralization (2.10 vs. 2.22 mmol/L, p < 0.05) was significantly reduced and alkaline phosphatase significantly rose (254 vs. 220 IU/L, p < 0.05) in the observation group. No significant difference was found in the growth rates of body weight, head circumference, or body length, either during the NICU hospitalization or during the 6-month follow-up after discharge (p > 0.05).
Conclusions:
Feeding premature infants of GA ≤34 weeks with EHF reduced the incidence of FI, but had no advantage in establishing whole intestinal nutrition, shortening parenteral nutrition (PN) time, or hospitalization time. It had little effect on physical growth or development during NICU hospitalization and within 6 months after discharge. However, it may increase the incidence of metabolic bone disease (MBD).
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