Caloric Composition and Nutritional Dosing
IV Nutrients
Substance |
kcal/g |
Common IV Concentration |
Dextrose |
3.6 |
70% |
Protein |
4 |
3.5-15% |
Lipids |
10 |
10%, 20%, and 30% (1, 2, and 3 kcal/mL) |
Micronutrient |
Quantity QD |
Notes |
Na |
1-2 mEq/kg |
Add as Cl, Acetate, or Phos |
K |
1-2 mEq/kg |
Add as Cl, Acetate, or Phos |
Phos |
20-40 mmol |
1 mmol Phos supplies 1.33 mEq Na or 1.47 mEq K, Add as far from Ca as possible |
Ca |
10-15 mEq |
Use Ca Gluconate, put in TPN 1st or Last |
Mg |
8-20 mEq |
Needed in Catabolic / Malnourished Pts |
Vitamins |
RDA |
All vitamins (ADEK, C, and B complexes) |
Trace Elements |
RDA |
Zn, Cu, Mn, Cr, Se |
Energy Needs
Harris-Benedict Equations
Male BMR=66+13.7Wt+5Ht−6.8AgeFemale BMR=655+9.6Wt+1.7Ht−4.7AgeWt(kg),Ht(cm)
TEE
Condition |
Goal kcal/kg/d |
Non-Stressed, Non-Depleted |
20-25 |
Trauma / Stress / Surgery / Critically Ill |
25-30 |
Major Burn |
35-40 |
Obesity |
22-25 (IBW) |
WtIBW<1.3⟹WtWtIBW>1.3⟹NWBWtIBW>1.5⟹IBWNBW=IBW+0.25(Wt−IBW)
Daily Protein Needs
Condition |
Goal g/kg/d |
Maintenance |
0.8-1 |
Repletion / Medical Floor |
1-1.5 |
Trauma / Surgery / ICU |
1.5-2 |
Burn |
2-2.5 |
Obesity |
2 (IBW) |
Nitrogen Balance
Determinant of protein status (negative balance indicates protein breakdown, positive indicates healing / protein synthesis).
Nitrogen Balance=24h Protein Intake (g)6.25+(24h UUN (g)+4(g))
Goal Nitrogen Balance: 0 for maintenance, (+)3-5 for repletion
Building a TPN
- Determine Total Daily Calories and Total Daily Protein
- Calculate Total Daily Non-Protein Calories
- Determine an appropriate Carb / Fat Ratio
- Typically 70%/30%, but can vary from 60-85%/15-40%
- Add Micronutrients PRN
Respiratory Quotient
RQ=vCO2vO2
RQ |
Predominately Oxidized Substance |
0.7 |
Fat |
0.8 |
Protein |
1 |
Carbs |
- Goal RQ: 0.85-0.95
- RQ > 1: Overfeeding and lipogenesis
Enteral Nutrition
Pre-made enteral nutrition solutions exist at 1 and 2 kcal/mL concentrations. 2 kcal/mL should be used in fluid restricted patients.
Administration Methods
- Continuous: Utilizes a pump, lower distention (and therefore aspiration) risk
- Intermittent: Several gravity based feeds of > 200mL over 20-30min
- Bolus: > 200mL over 5-10min (high aspiration risk)
- Cyclic: Administered over 8-20hr QD
Medication Administration Through Feeding Tubes
ISMP Do Not Crush List
If a medication can be crushed:
- Crush
- Administer w/ 5-30mL flush
- Repeat for each medication
- Give final flush
Monitoring
Test |
Initial |
QD |
PRN |
Chemsticks |
|
|
X |
I/Os |
X |
X |
|
Wt |
X |
X |
|
Feeding Tube Placement |
X |
|
X |
Gastric Residual Volume |
X |
|
X |
Abdominal Distention |
|
X |
|
# and Consistency of Stool |
|
X |
|
Contraindications
- Need less than 5-10d
- Severe pancreatitis
- High-output fistulas
- Inability to gain access
- Intractable V/D
- GI Ischemia
- Ileus
Complications
- Mechanical
- Clogging
- Aspiration
- Accidental Intubation and Aspiration
- Infection from airway / GI injury
- GI
- Gastroparesis
- GERD
- Diarrhea
- Constipation
- Metabolic
- Hyperglycemia
- Electrolyte and Vitamin Abnormalities
- Refeeding Syndrome
- Dehydration
Parenteral Nutrition
Peripheral Administration Limitations: NTE 12.5% Dextrose, NTE 900-1100 mOsm/L, NTE 5d per site
Cl vs Acetate
Typically given a 2/3 Cl, 1/3 Acetate. Alter as needed to aid management of Acid-Base balance according to SID.
Additional Additives
- H2 Antagonist (Famotidine)
- Insulin-R
- 0.1 U per 3.4 kcal dextrose (1g)
- For hyperglycemia
- High insulin additions should be switched to a separate insulin infusion
- Albumin should not be added as a protein source
Monitoring
Lab |
Initial |
QD (Unstable) |
1-2x weekly (Stable) |
PRN |
BUN, SCr, BG |
X |
X |
X |
|
Na, K, Cl, Bicarb, Mg, Ca, Phos |
X |
X |
X |
|
AST, ALT, LDH, Alk Phos, Bilirubin |
X |
|
X |
X |
GGT |
|
|
|
X |
Albumin |
X |
|
X |
X |
Prealbumin |
|
|
|
X |
TGs |
X |
|
X |
X |
Blood Panel |
|
|
|
X |
Vitamins and Trace Elements |
|
|
|
X |
TIBC, Ferritin |
|
|
|
X |
Lab |
Q8H |
QD |
PRN |
Volume Remaining of Infusion |
X |
|
|
I/Os |
X |
|
|
Wt |
|
X |
|
Temp |
X |
|
|
REE |
|
|
X |
Urine Gluc |
|
|
X |
Urine Lytes |
|
|
X |
UUN |
|
|
X |
Contraindications
- Functional GI Tract w/ Access
- Needed < 7d
Special Nutritional Populations
Pediatric Patients
CDC / WHO Growth Charts
Energy Requirements
Age |
kcal/kg/d |
Protein g/kg/d |
Preterm |
100-120+ |
3.5-4 |
0-6mo |
100-110 |
2-3 |
6-12mo |
90-100 |
1.5-2 |
1-7yr |
60-80 |
1-2 |
7-12yr |
50-60 |
1-1.2 |
12-18 |
30-50 |
0.8-0.9 |
*approx 40% of calories should be from fat
- Breastfeeding CIs
- HIV (+)
- Infectious TB
- Untreated Brucellosis
- Some Drugs
- Human T-cell Lymphotrophic Virus Infection
- Breast milk is approximately 20kcal/oz (50% fat)
- Cow’s milk is not an appropriate replacement
- Vitamin Supplementation
- Preterm Infants
- Vit D (< 1.5 kg): 200 U QD
- Vit D (≥ 1.5kg): 200-400 U QD
- Iron: 2 mg/kg QD (elemental)
- Term Infants
- Vit D 400 U QD if partially or fully breastfed
- Solid foods should be added at 4-6mo, 1 new food q4-5d
DM
- Moderate control of BG
- 110-220 in ill
- 140-180 in critically ill
- 30% total kcal as fat
- Give erythromycin or other kinetic agents for delayed gastric emptying in T1DM
CVD
- Avoid overfeeding
- Monitor fluid status
Short Bowel Syndrome
- w/ colon give high carb / low fat
- Consider B12 supplement
Renal Disease
- Fluid restriction
- Pre-Dialysis: Low Protein
- 0.5-0.8 g/kg (0.5-1 post-op)
- Dialysis: Normal Protein
- Intermittent HD: 1-1.3 g/kg
- CRRT: 1.5-2 g/kg
Pulmonary Failure
- 20-30 kcal/kg
- 30-50% of total kcal as fat
- Protein 1-2 g/kg
- Limit carbs (to decrease CO2 production)
Hepatic Disease
- 35 kcal/kg QD
- Standard protein (1-1.2 g/kg) w/o encephalopathy
- Protein restrict w/ encephalopathy (0.6 g/kg)
- Na restriction w/ ascites or edema
Misc
- GERD: Add H2 Antagonist or PPI
- NG Suction: Hyponatremia, hypokalemia, and/or hypochloremia which may need repletion
- N/V: Hypovolemia, Na imbalance, and/or hypokalemia
- Dialysis: Removes 10-20% of a.a.
- Wound Healing: Add Zn and Vit C
- Loop Diuretic Use: Watch electrolytes and correct
- Steroids: Monitor BG and consider insulin
Nutritional Disorders
Vitamin Deficiencies
Lipophilic Vitamins
- Vit A (retinoids and beta-carotene)
- Involved primarily in vision, but also as hormones
- Stored in the liver (and Vit A overdose can be hepatotoxic)
- Dietary sources include dark green vegetables, liver, egg yolk, and fatty dairy products
- Deficiency is rare, but can lead to night vision blindness
- Vit D (Cholecalciferol and Ergocalciferol)
- Provitamin D3 can be produced in the skin from 7-dehydrocholesterol
- A cis double bond in Pro-D3 is isomerized into D3 (cholecalciferol)
- Cholecalciferol and ergocalciferol (Vit D2 from plants) are then hydroxylated in the liver to form 25-hydroxy Vit D3, and again in the kidney to form 1,25-dihydroxy Vit D3 or calcitriol, the active biologic agent responsible for calcium homeostasis
- Deficiency is rare, but causes Rickets in children and Osteomalacia in adults
- Dietary sources include fortified milk, saltwater fish, liver, and egg yolk
- Vit E (Tocopherols and Tocotrienols)
- Function as potent antioxidants protecting unsaturated fatty acids
- May prevents LDL oxidation helping to prevent CVD
- Dietary sources are vegetable oils rich in polyunsaturated fatty acids
- Deficiency is rare
- Vit K
- Functions as an enzyme cofactor for the glutamate post-translational modification to carboxyglutamic acid, which is essential for allowing proteins to tightly bind Ca
- Vit K dependent post-translational modifications are required for bone mineralization (hydroxyapatite production) and coagulation (multiple clotting factors are Vit K dependent)
- Deficiency is rare
- Dietary sources include green, leafy vegetables for Vit K1 and gut bacterial synthesis for Vit K2
Hydrophilic Vitamins
- Vit B1 (Thiamin)
- Utilized as an enzyme cofactor in many enzymes via carbanion production, including many enzymes involved in glucose metabolism
- Severe deficiency is known as beriberi, which is characterized by muscle weakness
- Deficiency is most commonly seen in alcoholics, and administration of dextrose containing fluids in thiamin deficient patients can result in Wernicke’s Encephalopathy
- Pretreat w/ 100mg IM or slow IVPB in suspected deficiency
- May need up to 1000mg in the 1st 24hrs
- Chronic deficiency can also lead to Korsakoff’s psychosis, which is irreversible and responds poorly to antipsychotics (but they should still be used)
- Vit B2 (Riboflavin)
- Used as an enzyme cofactor (FAD and FMN)
- Deficiency is rare, but SSx include Cheilitis, Glossitis, and Scaly dermatitis, and is most commonly seen in alcoholics
- Dietary sources include milk, meat, eggs, and cereal products
- Vit B3 (Niacin)
- Converted to NAD and NADP
- Deficiency (pellagra) is common in pts with malabsorption diseases or alcoholics
- Pellagra presents with “The 3 D’s”: Dermatitis, Dementia, and Diarrhea
- Dietary sources include meats, peanuts, and enriched cereals
- Vit B6 (Pyridoxine)
- Pyridoxal phosphate is a cofactor for neurotransmitter and sphingolipid synthesis as well as amino acid metabolism
- Severe deficiency is uncommon, with SSx including irritability, nervousness, and depression in mild cases and peripheral neuropathy and Szs in severe deficiency
- Dietary sources include meats, vegetables, and whole-grain cereals
- Vit B7 (Biotin)
- Cofactor for the conversion of carboxylates to CO2
- Deficiency is somewhat rare, and most common in pregnant women
- Biotin binds incredibly tightly to avidin in egg whites (used throughout biochemical studies and assays, as well as a potential cause of deficiency)
- Vit B9 (Folate)
- Converted to tetrahydrofolate which is essential for one-carbon metabolism in a.a. and nucleotide synthesis
- Deficiency is most common in alcoholics, with notable SSx of macrocytic anemia and neural tube defects in children born to pregnant women with the deficiency
- Vit B12 (Cobalamin)
- Co containing “heme” group
- Required for two human biochemical reactions: methionine synthase (homocysteine into methionine) and methylmalonyl-CoA mutase (methylmalonyl-CoA into succinyl-CoA)
- Deficiency leads to homocysteine and methylmalonate accumulation causing macrocytic anemia and neurologic damage
- Deficiency can be dietary or “pernicious anemia” in which the absorptive cofactor (intrinsic factor) is absent or non-functioning
- Deficiency is most commonly seen in long-term vegetarians or malabsorption diseases
- Vit C (Ascorbic Acid)
- Cofactor for lysine hydroxylation (essential for collagen production)
- Reducing agent promoting iron absorption and protection of oxidation prone vitamins (A, E, and some B)
- Deficiency (Scurvy) marked by slow wound healing, decreased immunocompetency, osteoporosis, leading from mucosal membranes (especially the gums), and ulcerations across the body
Refeeding Syndrome
SSx
- Szs
- Coma
- Arrhythmias
- Lactic Acidosis
- Pulmonary Edema
- Fluid Overload
Monitoring
Prevention
- Correct electrolyte abnormalities first
- Start all patients at 50% goal caloric intake, high risk at 25% goal caloric intake
- Titrate to goal over 3-5d
- If SSx emerge decrease calories and correct emergent electrolyte problems
Kwashiorkor
Protein based malnutrition characterized by hypoalbuminemia, anemia, edema / ascites, muscle atrophy, impaired immune function, and delayed wound healing. Treat w/ slow introduction of food to avoid referring syndrome.
Marasmus
Caloric malnutrition characterized by wt loss, reduction of basal metabolic rate, depletion of fatty stores, bradycardia, and hypothermia. Treat w/ slow introduction of food to avoid referring syndrome.
Essential Fatty Acid Deficiency
SSx
- Dry Skin
- Immune Complications
- Thrombocytopenia
- Alopecia
- Peds
- Mental Development Delays
Treatment
4-10% of QD calories as Linoleic and Linolenic Acid
References