Fluids, Electrolytes, Acid-Base Disorders, and Nutrition Support
Product Category
Indication
Macronutrients
Additional
Comments
Examples
Increased protein
needs
Critically ill patients
(especially trauma,
surgical, burns)
1 kcal/mL
Protein 62 g/L
High-protein content,
fiber, isotonic
Replete, Promote
Glucose intolerance
Hyperglycemia,
diabetes
1.2 kcal/mL
Protein 60 g/L
Low-carbohydrate
content, fiber
Diabetisource
AC, Glucerna 1.2
Immune enhancing
Critically ill surgical
and trauma patients,
perioperative GI cancer
1.5 kcal/mL
Protein 90β94 g/L
Additional arginine,
glutamine; fish oil
Impact Peptide
1.5, Pivot
Bariatric
Patients with obesity
with good renal
function
1 kcal/mL
Protein 93 g/L
High protein, low
calories
Peptamen Intense
VHP
Elemental
Malabsorption, fat
intolerance
1β1.5 kcal/mL
Protein 50β68 g/L
Low fat/MCT, di/tri-
peptides/free AA, no
fiber, low residue
Vivonex RTF,
Vital
Protein supplement
High protein needs
10β15 g of protein
per serving is typical
(products vary)
Protein liquid, gel, or
powder
Pro-Stat, ProMod
AA = amino acids; MCT = medium-chain triglycerides.
Enteral nutrition β Medication interactions: Hold EN 1 hour before and after drug administration.
*Increase EN rate to account for time off EN.
Phenytoin (Nutr Clin Pract 1996;11:28-31)
Levothyroxine (J Endocrinol Invest 2014;37:583-7; Nutr Clin Pract 2010;25:646-52) - In one study,
liquid levothyroxine preparation was shown to alleviate need to hold EN. In lieu of holding EN,
increasing the levothyroxine dose by 25 mcg per day with weekly monitoring of thyroid function
tests has also been described. Care should be taken to reduce the dose back to the patientβs home
dose when they are transitioned off of EN if this option is chosen.
| d. | Itraconazole (Antimicrob Agents Chemother 1997;41:2714-8) |
|---|
Fluoroquinolones (J Antimicrob Chemother 1996;38:871-6)
*Some clinicians have empirically increased the dosage of these drugs while giving continuous
enteral feeding rather than holding the EN for 1 hour before and after drug administration. With
the exception of levothyroxine, this author discourages this practice, especially for warfarin and
phenytoin, because the doses necessary to overcome the effects of drug binding to the continuous
EN are potentially toxic when the EN is held or discontinued without a dose adjustment. Others
have increased the ciprofloxacin dose to 750 mg twice daily during continuous EN to achieve
therapeutic plasma concentrations well above the MIC (minimum inhibitory concentration) for a
gram-negative urinary tract infection (J Antimicrob Chemother 1996;38:871-6).