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Parenteral nutrition in neonate Goals • • • minimizes weight loss improves growth and neurodevelopmental outcome reduce the risk of mortality and NEC Caloric concentration A. Dextrose: 3.4 kcal/g. B. Protein: 4 kcal/g. C. Fat: 9 kcal/g. Carbohydrates 5 to 6 mg/kg per minute be required in the preterm infant to prevent hypoglycemia In ELBW neonate glucose starting at 3.5 mg/kg per minute (5 g/kg day) and slowly increasing to 12 mg/kg/min over several days Dextrose is provided to maintain blood sugar between 45 - 125 mg/dl In the presence of hyperglycemia, glucose infusion rate should not be reduced below 4 mg/kg/min. Insulin may be required to maintain adequate blood glucose levels, although its routine use is not recommended proteins Inadequate protein intake : Failure to thrive(lose 1 g/kg per day) Hypoalbuminemia Edema Amino acid intake produced positive nitrogen balance and appropriate growth Glutathione, an antioxidant concentrations rise with early amino acid administration Early amino acid supplementation may help decrease hyperglycemia and hyperkalemia Amino Acid Solations The ideal mixture of amino acids for PN in premature infants is unknow TrophAmine, Aminosyn PF, Aminoven are available that contain less of those potentially neurotoxic amino acids In preterm ELBW and VLBW infants, 3.5 g/kg/d of amino acids should be started on day 1 and is associated with better linear growth and neurodevelopmental outcomes. Term infants who are likely to have delayed initiation of enteral nutrition should be started on 1.5 g/kg/d of proteins Lipid Intravenous lipid administration provides essential fatty acids provides needed energy for tissue healing and growth combination of lipids and amino acids reduce episodes of hyperglycemia Starting lipids at 0.5–1 g/kg/d within 24 hours of birth is safe. Advance by 0.5–1.0 g/kg/d as tolerated up to 3.0 g/kg/d. The infusion is given continuously over 20–24 hours. The rate should not exceed 0.12–0.15 g/kg/h The use of 20% emulsions is preferred over 10% Lipids should be administered separately from amino acids caution may be needed in hyperbilirubinemia New lipid formulation(omegaven,smoflipid) Vitamins minerals Trace elements Heparin Monitoring Weight Daily Length Weekly Head circumference Weekly Intake and output Daily Glucose 2–3 times per day ; then as needed Calcium, phosphorus, 2–3 times per week; then every 1–2 weeks Electrolytes (Na, Cl, K, CO2) Daily , then 2–3 times per week. BUN and creatinine 2–3 per week; then every 1–2 weeks Bilirubin Weekly Ammonia Weekly if using high protein Total protein and albumin every 2–3 weeks AST/ALT every 2–3 weeks Triglycerides 1–2 per week Vitamins and trace minerals as indicated Urine Specific gravity and glucose 1–3 times per day initially; then as needed Intravenous routes used in PN A. Central PN. Central PN is usually reserved for patients requiring long-term(>2 weeks administration of most calories). Basically, this type of nutrition involves infusion of a hypertonic nutrient solution (15–30% dextrose) B. Peripheral PN. The maximum concentration of dextrose that can be administered is12.5% C. Umbilical catheters. PN can be given through an umbilical artery catheter but it is not preferred and should be used with caution. Maximum dextrose in UAC is 15%. cmplications nutrient-related : hypoglycemia (plasma sugar < 50 mg%) hyperglycemia (plasma sugar > 150 mg) Hyperammonemia metabolic acidosis (protein related); hypertriglyceridemia (triglyceride > 200mg/dl) Cholestasis ` Risk factors cholestasis : prematurity sepsis hypoxia hemodynamic instability duration of PN delayed entral feeding Catheter-related : malposition and infection pneumothorax pneumomediastinum, chylothorax Infection: Staphylococcus Pseudomonas spp, Klebsiella spp Candida albicans.