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Impact of early parenteral amino acid on preterm infant: A multicenter study
Yi-Yu Lin1, Chia-Huei Chen2, Ming-Luen Tsai3
1Division of Neonatology, Department of Pediatrics, MacKay Children's Hospital, Taipei, Taiwan.
Insights
Early parenteral amino acid (AA) administration improves feeding efficiency in very low birth weight (VLBW) infants. Higher AA doses are linked to better growth and reduced morbidities like bronchopulmonary dysplasia (BPD) and patent ductus arteriosus (PDA).
Area of Science:
- Neonatal Medicine
- Nutritional Science
- Pediatric Critical Care
Background:
- Early nutrition is critical for the growth and neurodevelopment of preterm infants, particularly those with very low birth weight (VLBW).
- Parenteral nutrition, including amino acids (AAs), plays a vital role in supporting these vulnerable infants.
Purpose of the Study:
- To evaluate the impact of early parenteral amino acid (AA) administration on growth outcomes in VLBW infants.
- To assess the effects of AA timing and dosage on feeding patterns and short-term neonatal morbidities.
Main Methods:
- A multicenter retrospective cohort study involving VLBW infants (<32 weeks gestation) from 2019-2023.
- Infants were categorized by parenteral AA initiation time (≤24h vs. >24h) and initial dose (≤2.5g/kg/day vs. >2.5g/kg/day).
- Clinical outcomes and nutritional practices were compared across these groups.
Main Results:
- Earlier AA initiation was associated with a shorter time to achieve full feeding (23.4 vs. 26.2 days).
- Higher initial AA doses led to earlier achievement of full feeding (21.6 vs. 25.5 days) and higher nadir body weights.
- The high-dose AA group showed significantly lower rates of treated patent ductus arteriosus (PDA), pulmonary hemorrhage, and moderate-to-severe bronchopulmonary dysplasia (BPD).
- Multivariate analysis confirmed that initial AA dose was independently associated with reduced risks of BPD and PDA.
Conclusions:
- Early initiation and higher doses of parenteral AAs are linked to improved feeding efficiency in VLBW infants.
- Higher AA doses may reduce the incidence of significant neonatal morbidities, including PDA and BPD.
- Further research is needed to establish optimal parenteral AA dosing strategies for VLBW infants.
Background:
Early nutrition is essential for the growth and neurodevelopment of preterm infants, especially those with very low birth weight (VLBW). This multicenter retrospective cohort study aimed to evaluate the effects of early parenteral amino acid (AA) administration on growth outcomes, feeding patterns, and short-term neonatal outcomes.
Methods:
This study included VLBW infants (<32 weeks of gestation) treated in six tertiary neonatal intensive care units across Taiwan between 2019 and 2023. Participants were grouped based on the timing of parenteral AA initiation (≤24 h or > 24 h after birth) and initial dose (≤2.5 g/kg/day or > 2.5 g/kg/day). Clinical outcomes and nutritional practices were compared across the groups.
Results:
Among the 959 infants, who received AAs earlier, the time to achieve full feeding was significantly shorter (23.4 ± 13.3 days vs. 26.2 ± 11.4 days, p = 0.035) compared to those who received AAs later. Among the 973 infants, infants receiving higher doses of AAs reached full feeding earlier (21.6 ± 14 days vs. 25.5 ± 12 days, p < 0.001) and had higher nadir body weights (981.1 ± 247.5 g vs. 941.8 ± 264.4 g, p = 0.028). Short-term outcomes, such as patent ductus arteriosus (PDA) requiring treatment (13.3 % vs. 19 %, p = 0.019), pulmonary hemorrhage (2.9 % vs. 5.7 %, p = 0.036), and moderate to severe bronchopulmonary dysplasia (BPD) (45.6 % vs. 54.3 %, p = 0.01), were significantly lower in the high-dose group. Multivariate logistic regression analysis revealed that the initial AA dose was independently associated with decreased risks of BPD and PDA.
Conclusion:
Early initiation and higher doses of parenteral AAs were associated with improved feeding efficiency and reduced morbidities, such as PDA and BPD, in VLBW infants. Further large-scale and long-term studies are required to confirm these findings and determine the optimal dosing strategies.
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