Hypertriglyceridaemia in extremely preterm infants receiving parenteral lipid emulsions
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Published on: January 12, 2018
Ruth Sinclair1, Tim Schindler1,2, Kei Lui1,2
1Royal Hospital for Women, Randwick, NSW, Australia.
Insights
Hypertriglyceridemia is common in preterm infants receiving parenteral lipid emulsions. Monitoring and adjusting lipid intake can mitigate potential consequences.
Area of Science:
- Neonatal Medicine
- Clinical Nutrition
- Pediatric Critical Care
Background:
- Parenteral nutrition in neonates frequently includes lipid emulsions (LE).
- Clinical practices for monitoring plasma triglycerides during LE therapy vary widely.
- Hypertriglyceridemia is a potential concern in this vulnerable population.
Purpose of the Study:
- To evaluate the incidence of hypertriglyceridemia (Plasma triglyceride > 2.8 mmol/L) in extremely preterm infants.
- To assess the association between hypertriglyceridemia and mortality or major morbidities.
- To inform clinical practice regarding LE administration in neonates.
Main Methods:
- Retrospective review of 195 infants < 29 weeks gestation.
- Standardized LE administration protocol with stepwise increase and triglyceride monitoring.
- Dosage adjustment to maintain plasma triglycerides ≤ 2.8 mmol/L.
Main Results:
- Hypertriglyceridemia occurred in 32.5% of infants aged 23-25 weeks and 16.1% aged 26-28 weeks.
- Severe hypertriglyceridemia (> 4.5 mmol/L) was observed in 10.0% and 4.5% of the respective groups.
- Univariate analysis suggested associations with mortality and retinopathy of prematurity, which were non-significant in multivariate analysis.
Conclusions:
- Hypertriglyceridemia is a frequent complication in extremely preterm infants on parenteral lipid emulsions.
- Regular monitoring and prompt adjustment of lipid emulsion dosage are crucial.
- Minimizing exposure to hypertriglyceridemia may help mitigate adverse outcomes.
Background:
Lipid emulsions (LE) are routinely administered as part of parenteral nutrition in neonates. There is a wide variation in clinical practice of plasma triglyceride monitoring during LE therapy. Our aim was to evaluate the incidence of hypertriglyceridaemia (Plasma triglyceride > 2.8 mmol/L) and its association with mortality and major morbidities in extremely preterm infants on parenteral nutrition.
Methods:
A retrospective review of 195 infants < 29 weeks gestation. Lipid emulsion was commenced at 1 g/kg/day soon after birth and increased by 1 g/kg daily up to 3 g/kg/day and continued until the infant was on at least 120 ml/kg/day of enteral feeds. Plasma triglyceride concentrations were measured at each increment and the lipid emulsion dosage was adjusted to keep plasma triglyceride concentrations ≤2.8 mmol/L.
Results:
Hypertriglyceridemia was noted in 38 neonates (32.5% in 23-25 weeks and 16.1% in 26-28 weeks). Severe hypertriglyceridemia (> 4.5 mmol/L) was noted in 11 infants (10.0% in 23-25 weeks and 4.5% in 26-28 weeks). Hypertriglyceridemia was associated with an increase in mortality (unadjusted OR 3.5; 95% CI 1.13-10.76; 0.033) and severe retinopathy of prematurity (unadjusted OR 4.06; 95% CI 1.73-9.59; 0.002) on univariate analysis. However, this association became non-significant in multivariate analysis with adjustment for gestation and birthweight.
Conclusions:
Hypertriglyceridemia is common in extremely preterm infants receiving parenteral lipid emulsions. Regular monitoring and prompt adjustment of lipid intake in the presence of hypertriglyceridemia, minimising the length of exposure to hypertriglyceridemia, may mitigate potential consequences.
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