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Identifying a Safety Threshold for Parenteral Glucose Intake in the Early Acute Phase of Preterm Neonates
Maria Di Chiara1, Ilaria Mastropasqua1, Flavia Gloria1
1Department of Maternal-Infantile and Urological Sciences, Policlinico Umberto I, Sapienza University of Rome, Viale del Policlinico 155, 00161 Rome, Italy.
Insights
Exceeding 7 g/kg/day of parenteral dextrose in preterm neonates is linked to early hyperglycemia and hypertriglyceridemia. This study suggests a potential safety threshold for glucose intake, though further research is needed for clinical guidelines.
Area of Science:
- Neonatalogy
- Pediatric Endocrinology
- Clinical Nutrition
Background:
- Parenteral glucose safety in preterm neonates is not well-established.
- International guidelines offer recommended ranges, but specific safety thresholds require investigation.
- Early acute phase nutrition is critical for preterm infant outcomes.
Purpose of the Study:
- To determine if exceeding a data-driven parenteral dextrose intake threshold is associated with adverse outcomes in preterm neonates.
- To evaluate associations with hyperglycemia, hypertriglyceridemia, metabolic acidosis, and extrauterine growth restriction (EUGR).
- To identify a potential safety threshold for parenteral glucose administration.
Main Methods:
- Single-center retrospective study of preterm neonates (gestational age ≤ 34 weeks and/or birth weight ≤ 1500 g).
- Data-driven threshold identification using restricted cubic spline logistic regression.
- Multivariable analyses adjusted for key neonatal and perinatal factors.
Main Results:
- A parenteral dextrose intake threshold of 7 g/kg/day was identified.
- Exceeding this threshold was independently associated with hyperglycemia (aOR 5.55) and hypertriglyceridemia (aOR 4.36).
- No significant association was found with metabolic acidosis or EUGR.
Conclusions:
- Parenteral dextrose intake above 7 g/kg/day is linked to early metabolic complications in preterm infants.
- The findings suggest a potential safety threshold for parenteral glucose within recommended ranges.
- Prospective multicenter studies are necessary to inform clinical recommendations.
Abstract:
Background/Objectives: The safety of specific parenteral glucose intake values within the range currently recommended by international guidelines for the early acute phase in preterm neonates has not been established. This study aimed to evaluate whether exceeding a data-driven parenteral dextrose intake threshold during the first week of life is independently associated with hyperglycemia, hypertriglyceridemia, metabolic acidosis, and extrauterine growth restriction (EUGR). Methods: This was a single-center retrospective study involving preterm neonates (gestational age ≤ 34 weeks and/or birth weight ≤ 1500 g) admitted to the Neonatal Intensive Care Unit of Policlinico Umberto I, Rome, between 2015 and 2022. The analysis followed two pre-specified steps: (1) data-driven identification of an exposure threshold by restricted cubic spline logistic regression; (2) multivariable analyses with the dichotomized exposure, adjusting for gestational age, birth weight, enteral nutrition timing, neonatal morbidity, and perinatal compromise. Results: 389 preterm neonates met eligibility. The data-driven inflection point of the spline-derived log-odds curve identified a threshold of 7 g/kg/day. Exceeding this threshold during the first week of life was independently associated with both hyperglycemia (adjusted odds ratio 5.55, 95% confidence interval 2.56 to 12.03; p < 0.001) and hypertriglyceridemia (adjusted odds ratio 4.36, 95% confidence interval 1.41 to 13.45; p = 0.010), but not with metabolic acidosis or with EUGR at 36 weeks postmenstrual age. The divergence in daily parenteral glucose intake between cases and controls was apparent from the second day of life. Conclusions: Exceeding 7 g/kg/day of parenteral dextrose was independently associated with early metabolic complications, but not with growth outcomes. A safety threshold for parenteral glucose may exist within the currently recommended intake range; prospective multicenter studies are needed before clinical recommendations can be drawn.
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