Drug Guide
Amino Acids (various formulations)
Classification
Therapeutic: Nutritional Support
Pharmacological: Amino Acid Mixture
FDA Approved Indications
- Parenteral nutrition in patients requiring amino acid supplementation
- Supporting metabolic needs when oral nutrition is not feasible
Mechanism of Action
Provides essential and non-essential amino acids directly into the bloodstream, supporting protein synthesis and metabolic functions.
Dosage and Administration
Adult: Dose varies based on nutritional needs; typically 0.8-2.0 g amino acids/kg/day via IV infusion.
Pediatric: Dosed according to age and weight; commonly 0.5-2 g/kg/day under medical supervision.
Geriatric: Adjusted based on renal and hepatic function; require careful monitoring.
Renal Impairment: Dose adjustments required; monitor renal function and electrolytes.
Hepatic Impairment: Use with caution; avoid in hepatic encephalopathy unless monitored closely.
Pharmacokinetics
Absorption: Not applicable (administered parenterally).
Distribution: Distributed throughout body water compartments.
Metabolism: Metabolized in tissues; catabolized in liver or peripherally as proteins.
Excretion: Excreted mainly via urine as nitrogenous waste.
Half Life: Varies depending on the specific formulation and patient condition.
Contraindications
- Allergy to amino acids or components
- Metabolic disorders contraindicating amino acid infusion
Precautions
- Monitor renal and hepatic function during therapy
- Use caution in patients with fluid overload or electrolyte abnormalities
- Pregnancy and lactation: consult specific product labeling
Adverse Reactions - Common
- Pain or phlebitis at infusion site (Rare)
- Electrolyte disturbances (Uncommon)
Adverse Reactions - Serious
- Anaphylaxis (Rare)
- Metabolic disturbances, including azotemia (Uncommon)
Drug-Drug Interactions
- May interact with medications affecting renal or hepatic function
- Certain alkali solutions may interact with amino acid infusions
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor infusion site, fluid status, electrolyte levels, and liver/kidney function.
Diagnoses:
- Risk for electrolyte imbalance
- ineffective tissue perfusion related to infusion complications
Implementation: Administer as prescribed, rotate infusion site, and monitor patient response.
Evaluation: Assess nutritional status, laboratory parameters, and infusion site regularly.
Patient/Family Teaching
- Report any pain, swelling, or redness at infusion site immediately.
- Understand that this is for nutritional support and will be given intravenously.
- Follow instructions regarding infusion timing and monitoring.
Special Considerations
Black Box Warnings: N/A
Genetic Factors: None specified.
Lab Test Interference: May affect nitrogen balance tests and serum protein levels.
Overdose Management
Signs/Symptoms: Electrolyte imbalance, fluid overload, metabolic disturbances.
Treatment: Discontinue infusion, supportive care, correct electrolytes and fluid status.
Storage and Handling
Storage: Store in a cool, dry place; protect from light.
Stability: Stable until expiration date when unopened; follow specific product guidelines.