alanine + arginine + aspartic acid + 22 other active ingredients: prescribing and clinical use
Focused clinical detail for use alongside current product information, local policy and patient-specific assessment.
alanine + arginine + aspartic acid + 22 other active ingredients: clinical details
Prescribing considerations
- Confirm that oral or enteral nutrition is impossible, insufficient or contraindicated.
- Assess the complete nutrient, fluid and electrolyte contribution; a fixed multi-chamber composition may not meet every individual requirement.
- Correct severe fluid, electrolyte or metabolic disturbances before initiation.
- Use controlled central-venous administration and strict aseptic catheter care.
- Consider additional vitamins and trace elements because intrinsic quantities are insufficient.
- Use caution in hepatic or renal impairment, diabetes, hyperlipidaemia, coagulation disorders, anaemia, heart failure, pulmonary dysfunction and patients at risk of refeeding-related shifts.
Contraindications and cautions
- Premature neonates, infants and children younger than 2 years
- Hypersensitivity to egg, soya-bean, peanut or corn products, or another ingredient
- Congenital amino-acid metabolism abnormalities
- Severe hyperlipidaemia or severe lipid-metabolism disorder with hypertriglyceridaemia
- Severe hyperglycaemia
- Pathologically elevated sodium, potassium, magnesium, calcium or phosphorus concentrations
Monitoring
- Fluid and electrolyte balance, serum osmolarity and acid–base status
- Blood glucose and, where relevant, urine glucose and ketones
- Serum triglycerides and lipid clearance
- Liver and kidney function; consider ammonia if hepatic impairment is suspected
- Full blood count, platelets and coagulation tests
- Catheter site, line integrity and signs of infection, sepsis, extravasation or precipitate formation
Clinical pharmacology
This combination supplies amino-acid nitrogen for protein synthesis, glucose and olive/soya triglycerides for energy, and electrolytes for physiological balance. Its constituents follow their usual individual metabolic and elimination pathways.
Formulation and product differences
- Three-compartment bag containing an amino-acid/electrolyte solution, glucose with calcium, and an olive-oil/soya-bean-oil lipid emulsion.
- The mixed product is a high-osmolarity, homogeneous milky emulsion intended only for central-venous administration.
- Contains electrolytes; their existing contribution must be considered before compatible additions are made.
- Contains purified egg phospholipids and corn-derived glucose as well as refined soya-bean oil.
alanine + arginine + aspartic acid + 22 other active ingredients interactions
Compatibility with other intravenous treatments and effects on potassium require particular attention.
Ceftriaxone
Calcium-containing solutions can form ceftriaxone-calcium precipitates, so simultaneous administration or mixing is restricted and lines require appropriate separation or flushing.
Potassium-sparing diuretics
Medicines such as amiloride, spironolactone and triamterene can increase the risk of hyperkalaemia because this formulation contains potassium.
ACE inhibitors and angiotensin II receptor antagonists
Combined use can increase the risk of hyperkalaemia and requires attention to potassium levels.
Sources
These sources were used to prepare and review this medicine page.
Prepared and reviewed by the iatroX editorial team.