Safety and efficacy of early parenteral lipid and high-dose amino acid administration to very low birth weight infants

J Pediatr. 2013 Sep;163(3):638-44.e1-5. doi: 10.1016/j.jpeds.2013.03.059. Epub 2013 May 6.

Abstract

Objective: To assess the efficacy and safety of early parenteral lipid and high-dose amino acid (AA) administration from birth onwards in very low birth weight (VLBW, birth weight <1500 g) infants.

Study design: VLBW infants (n = 144; birth weight 862 ± 218 g; gestational age 27.4 ± 2.2 weeks) were randomized to receive 2.4 g of AA kg(-1) · d(-1) (control group), or 2.4 g AA kg(-1) · d(-1) plus 2-3 g lipids kg(-1) · d(-1) (AA + lipid group), or 3.6 g AA kg(-1) · d(-1) plus 2-3 g lipids kg(-1) · d(-1) (high AA + lipid group) from birth onwards. The primary outcome was nitrogen balance. The secondary outcomes were biochemical variables, urea rate of appearance, growth rates, and clinical outcome.

Results: The nitrogen balance on day 2 was significantly greater in both intervention groups compared with the control group. Greater amounts of AA administration did not further improve nitrogen balance compared with standard AA dose plus lipids and was associated with high plasma urea concentrations and high rates of urea appearance. No differences in other biochemical variables, growth, or clinical outcomes were observed.

Conclusions: In VLBW infants, the administration of parenteral AA combined with lipids from birth onwards improved conditions for anabolism and growth, as shown by improved nitrogen balance. Greater levels of AA administration did not further improve the nitrogen balance but led to increased AA oxidation. Early lipid initiation and high-dose AA were well tolerated.

Keywords: AA; Amino acid; ECF; Ethyl chloroformate; NICU; Neonatal intensive care unit; ROP; Retinopathy of prematurity; SGA; Small for gestational age; TG; Triacylglycerol; VLBW; Very low birth weight.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Amino Acids / administration & dosage*
  • Biomarkers / blood
  • Biomarkers / urine
  • Double-Blind Method
  • Female
  • Humans
  • Infant, Newborn
  • Infant, Very Low Birth Weight / growth & development
  • Infant, Very Low Birth Weight / metabolism
  • Infant, Very Low Birth Weight / physiology*
  • Linear Models
  • Lipids / administration & dosage*
  • Logistic Models
  • Male
  • Nitrogen / urine
  • Parenteral Nutrition / methods*
  • Parenteral Nutrition Solutions / administration & dosage
  • Parenteral Nutrition Solutions / chemistry*
  • Urea / blood

Substances

  • Amino Acids
  • Biomarkers
  • Lipids
  • Parenteral Nutrition Solutions
  • Urea
  • Nitrogen