-
Caloric need:
approximately 25 kcal/kg/day
-
Composition of a Standard Central Venous Solution:
- Volume:
- 10% Amino Acid solution- 500ml
- 50% dextrose solution -500ml
- Fat emulsion -
- Electrolytes+vitamins+minerals - ~50ml
- Total volume: ~ 1,050
- Composition:Amino acids- 50g
- Dextrose- 250g
- Total N- 8g = (50/6.25)
- Dextrose kcal: 840kcal = (250g x 3.4kcal/g)
- MOsms/L: ~2,000
-
Electrolytes added to TPN (total parenteral nutrition) solutions:
Electrolyte/Usual Concentration/ Range of Concentrations
- Sodium: 60 (0-150)
- Potassium: 40 (0-80)
- Acetate: 50 (50-150)
- Chloride: 50 (0-150)
- Phosphate: 15 (0-30)
- Calcium 4.5 (0-20)
- Magnesium: 5 (5-15)
-
How many kcal/g in:
Fat:
Protein:
Oral carbohydrates:
Dextrose:
10% lipid:
20% lipid solution:
- Fat: 9 kcal/g
- Protein: 4 kcal/g
- Oral carbohydrates: 4 kcal/g
- Dextrose: 3.4 kcal/g
- 10% lipid solution: 1.1 kcal/cc
- 20% lipid solution: 2 kcal/cc
-
Nutritional requirements for average healthy adult male:
- 1) 1g protein/kg/day is needed, of which 20% should be essential amino acids
- 2) 30% fat calories- important for essential fatty acids
- 3) rest of calories should be as carbohydrates
-
What factors can increase the kcal requirement, and by how much?
- 1) Trauma, surgery, or sepsis stress can increase kcal requirement 20-40%
- 2) Pregnancy increases kcal requirement 300kcal/day
- 3) Lactation increases kcal requirement 500kcal/day
- 4) Protein requirement also increases with these
-
Burns:
- Calories: 25 kcal/kg/day + (30 kcal/day x % burn)
- Protein: 1-1.5 g/kg/day + (3g x % burn)
-
What is much of the energy expenditure used for?
heat production
-
What happens to the basal metabolic rate in relation to temperature?
Basal metabolic rate increases 10% for each degree above 38C
-
If overweight, use the following equation to determine patient's weight:
- Weight =
- [(actual weight- ideal body weight) x 0.25]+ IBW
-
What is the Harris-Benedict Equation:
- Harris-Benedict equation calculates basal energy expenditure based on:
- 1) weight
- 2) height
- 3) age
- 4) gender
-
Central line TPN:
- 1) glucose based
- 2) maximum glucose administration: 3g/kg/h
-
Peripheral line parenteral nutrition (PPN):
fat based
-
See table on pg 44: Metabolic Differences between the response to simple starvation and injury
-
What is the fuel for colonocytes?
short-chain fatty acids
-
Glutamine
- 1) fuel for small bowel enterocytes
- 2) most common amino acid in bloodstream and tissue
- 3) releases NH4 in the kidney, thus helping with nitrogen excretion
- 4) can be used for gluconeogenesis
-
What is the primary fuel for neoplastic cells:
glutamine
-
Preoperative nutritional assessment (following slides):
-
Approximate half-lives of:
Albumin:
Transferrin:
Prealbumin:
- Albumin: 20 days
- Transferrin: 10 days
- Prealbumin: 2 days
-
Normal protein level:
6.0-8.5
-
Normal albumin level:
3.3-5.5
-
Acute indicators of nutritional status:
- 1) retinal binding protein
- 2) prealbumin
- 3) transferrin
- 4) total lymphocytes count
-
Ideal body weight (IBW)
- Men= 106 lb + 6 lbs for each inch over 5 ft
- Women= 100 lb + 5 lbs for each inch over 5 ft
-
Preoperative signs of poor nutritional status:
- 1) acute weight loss >10% in 6 months
- 2) weight <85% of IBW
- 3) Albumin <3.0
- 4) low albumin (<3.0)- strong risk factor for morbidity and mortality after surgery
-
Respiratory Quotient (RQ)
1) Ratio of CO 2 produced to O 2 consumed- measurement of energy expenditure
- 2) RQ>1= lipogenesis (overfeeding)
- 1- Tx: decrease carbohydrates and caloric intake
- 2- high carbohydrate intake can lead to CO2
- 3- buildup and ventilator problems
- 3) RQ<0.7= ketosis and fat oxidation (starving)
- 1- Tx increase carbohydrates and caloric intake
- 4)
- Pure fat metabolism: RQ= 0.7
- Pure protein metabolism- RQ=0.8
- Pure carbohydrate metabolism- RQ=1
-
Postoperative phases
- 1) Diuresis phase- postoperative days 2-5
- 2) Catabolic phase- postoperative days 0-3 (negative nitrogen balance)
- 3) Anabolic phase- postoperative days 3-6 (positive nitrogen balance)
-
Starvation or major stress (surgery trauma, systemic illness)- slides to follow
-
Glycogen stores:
- 1) depleted after 24-36 hours of starvation (2/3 in skeletal muscle, 1/3 in liver)--> body then switches to fat
- 2) skeletal muscle lacks glucose-6-phosphatase (found only in liver)
- 3) glucose-6-phosphate stays in muscle after breakdown from glycogen and is utilized
-
Gluconeogenesis precursors:
- 1) amino acids (especially alanine), lactate, pyruvate, glycerol
- 2) Alanine is the simplest amino acid precursor for gluconeogenesis
- 1- primary substrate for gluconeogenesis
- 3) Alanine and phenylalanine- only amino acids to increase during time of stress
- 4) Late starvation- gluconeogenesis occurs in kidney
-
Starvation
- 1) protein-conserving mechanisms do not occur after trauma or surgery) secondary to catecholamines and cortisol
- 2) protein-conserving mechanisms do occur in starvation3) Fat (ketones) is the main source of energy in trauma and starvation
- 4) most patients can tolerate a 15% weight loss without major complications
- 5) patients can tolerate about 7 days without eating; if longer than that, place a Dobhoff tube or start TPN
- 6) try to feed gut to avoid bacterial translocation (bacterial overgrowth, increased permeability due to starved enterocytes)
- 7) Elemental formula- all protein given in the form of amino acids (given IV, expensive)
- 8) PEG- consider when regular feeding not possible (i.e. CVA) or predicted to not occur for >4 weeks
-
What energy does brain use?
Brain- utilizes ketones with progressive starvation (normally uses glucose)
-
Name structures that are obligate glucose users:
- 1) peripheral nerves
- 2) adrenal medulla
- 3) red blood cells
- 4) white blood cells
-
Refeeding syndrome
- 1) occurs when feeding after prolonged starvation/malnutrition
- 2) results in decreased K, Mg, and PO4; causes cardiac dysfunction and fluid shifts
- 3) prevent this by starting at a low rate (10-15 kcal/kg/day)
-
Cachexia
- 1) anorexia, weight loss, starvation/malnutrition
- 2) thought to be mediated by TNF-alpha
- 3) glycogen breakdown, lipolyisis, protein catabolism
-
Kwashiorkor
protein deficiency
-
-
See image on pg 46: Homeostatis adjustments initiated after injury
-
Nitrogen balance:
- 1) 6.25g of protein contains 1g of nitrogen
- 2) N balance= (N in - N out)= ([protein/6.25] - [24hour urine N + 4 g])
- 1- Positive N balance- more protein ingested than excreted (anabolism)
- 2- Negative N balance- more protein excreted than taken in (catabolism)
- 3) total protein synthesis for a healthy, normal 70kg male is 250g/day
-
Liver
- 1) responsible for amino acid production and breakdown
- 2) Urea production to get rid of ammonia from amino acid breakdown
- 3) majority of protein breakdown from skeletal muscle is glutamine and alanine
-
Fat Digestion
- 1) Triacylglycerides (TAG), cholesterol, and lipids
- 1- broken down by pancreatic lipase, cholesterol esterase, and phospholipase to micelles and free fatty acids
- 2- Micelles- aggregates of bile salts, long-chain free fatty acids, and monoacylglycerides
- a- enter enterocytes by fusing with membrane
- b- Bile salts- increase absorption area for fats, helping form micellesc- Cholesterol- used to synthesize bile salts
- d- fat soluble vitamins (A,D,E,K)- absorbed in micelles
- 2) Medium and short chain fatty acids- enter enterocyte by simple diffusion
- 3) Micelles and other fatty acids enter enterocytes--> chylomicrons are formed, which enter lymphatics (thoracic duct)
- 4) Chylomicrons- 90% TAGs, 10% phospholipids/proteins/cholesterol
- 1- medium-and short-chain fatty acids- enter portal system (same as amino acids and carbohydrates
- 2- long chain fatty acids- enter lymphatics along with chylomicrons
-
Lipoprotein lipase-
on liver endothelium, clears chylomicrons and TAGs from the blood, breaking them down to fatty acids and glycerol, which are then taken up by hepatocyte
-
Free fatty acid-binding protein
- 1) on liver endothelium
- 2) binds short and medium chain fatty acids
-
VLDL
most important route of entry for dietary cholesterol; synthesized in liver
-
Saturated fatty acids
- 1) used for fuel by cardiac and skeletal muscles
- 1- Fatty acids (ketones- acetoacetate, beta-hydroxybutyrate)- preferred source of energy for the liver, heart, and skeletal muscle
-
Unsaturated fatty acids
used as structural components for cells
-
Hormone-sensitive lipase:
- 1) in fat cells
- 2) breaks down TAGs (storage form of fats) to fatty acids and glycerol; released into blood (sensitive to growth hormone, catecholamines, glucocorticoids)
-
Essential fatty acids-
- 1) linolenic, linoleic
- 2) needed for prostaglandin synthesis (long-chain fatty acids)
- 3) important for immune cells
-
Omega-3-fatty acids:
- All odd- thought to have antioxidant properties
- 1) PGI3
- 2) TXA3
- 3) LTB5
-
-
Omega-6-fatty acids
- All even
- 1) PGE2
- 2) TXA2
- 3) LTB4
-
Carbohydrate digestion:
- 1) begins with salivary amylase, then pancreatic amylase and disaccharidases
- 2) Glucose and galactose- abosrbed by secondary active transport; released into portal vein
- 3) Fructose- facilitated diffusion; released into portal vein
- 4)
- Sucrose- fructose + glucose
- Lactose- galactose + glucose
- Maltose- glucose + glucose
-
Protein Digestion:
- 1) begins with:
- 1- stomach pepsin2- then trypsin, chymotripsin, and carboxypeptidase
- 2) Trypsinogen released from pancreas and activated by enterokinase released from duodenum
- 1- other pancreatic protein enzymes are then activated by trypsin
- 2- trypsin can then also autoactivate other trypsinogen molecules
- 3) Protein broken down to amino acids, dipeptides, and tripeptides by proteases
- 4) absorbed by secondary active transport; released as free amino acids into portal vein
- 5) may want to limit protein intake in patients with liver failure and renal failure to avoid ammonia buildup and possible worsening encephalopathy
-
Branched-chain amino acids-
- 1) leucine
- 2) isoleucine
- 3) valine
- (acronym: "LIV")
- 1) metabolized in muscle
- 2) possibly important in patients with liver failure
- 3) are essential amino acids
-
Cori cycle:
- 1) glucose is utilized and converted to lactate in muscle
- 2) lactate then goes to the liver and is converted back to pyruvate and eventually glucose via gluconeogenesis3) glucose is then transported back to muscle
-
Deficiencies:
Chromium-
Selenium-
Copper-
Zinc-
Trace elements-
Phosphate-
Thiamine (B1)-
Pyridoxine (B6)-
Cobalamine (B12)-
Folate-
Niacin-
Essential fatty acids-
Vitamin A-
Vitamin K-
Vitamin D-
Vitamin E-
- Chromium- hyperglycemia, encephalopathy, neuropathy
- Selenium- cardiomyopathy, weakness, hair loss
- Copper- pancytopenia
- Zinc- hair loss, poor healing, rash
- Trace elements- poor wound healing
- Phosphate- weakness (failure to wean off ventilator), encephalopathy, decrease phagocytosis
- Thiamine (B1)- wernicke's encephalopathy, cardiomyopathy, peripheral neuropathy
- Pyridoxine (B6)- sideroblastic anemia, glossitis, peripheral neuropathy
- Cobalamine (B12)- megaloblastic anemia, peripheral neuropathy, beefy tongue
- Folate- megaloblastic anemia, glossitis
- Niacin- pellagra (diarrhea, dermatitis, dementia)
- Essential fatty acids- dermatitis, hair loss, thrombocytopenia
- Vitamin A- night blindness
- Vitamin K- coagulopathy
- Vitamin D- rickets, osteomalacia
- Vitamin E- neuropathy
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