glucose monohydrate + magnesium chloride hexahydrate + potassium chloride + sodium acetate trihydrate + sodium chloride: prescribing and clinical use
Focused clinical detail for use alongside current product information, local policy and patient-specific assessment.
glucose monohydrate + magnesium chloride hexahydrate + potassium chloride + sodium acetate trihydrate + sodium chloride: clinical details
Prescribing considerations
- Base selection on the indication, intake and losses, comorbidities, concomitant treatment, and clinical and laboratory response.
- Assess risks of fluid overload, acute hyponatraemia, hyperglycaemia, hyperkalaemia, hypermagnesaemia and alkalosis.
- Use particular caution with cardiac, pulmonary or renal impairment, diabetes, hypocalcaemia, myasthenia gravis, cerebral pathology and sodium-retaining states.
- Consider refeeding risk in severe malnutrition or prolonged starvation.
- It contains no calcium and is unsuitable for correcting symptomatic hypomagnesaemia or severe metabolic or respiratory acidosis.
- Paediatric safety and effectiveness are not adequately established; specialist assessment and close biochemical monitoring are required.
Contraindications and cautions
- Hyperkalaemia.
- Severe renal insufficiency with oliguria or anuria.
- Uncompensated cardiac or pulmonary failure.
- Uncontrolled diabetes, known glucose intolerance, hyperosmolar coma, hyperglycaemia or hyperlactataemia.
- Hypersensitivity to an active substance or excipient.
- The initial period following head trauma because the solution contains glucose.
Monitoring
- Fluid balance, urine output and signs of oedema or pulmonary congestion.
- Serum sodium, potassium, magnesium and other relevant electrolytes.
- Blood glucose, particularly in diabetes, newborns and cerebral pathology.
- Blood and urine acid–base status where clinically relevant.
- The infusion site for phlebitis, thrombosis, infection or extravasation.
- Signs of hypersensitivity, hypermagnesaemia and refeeding-related disturbance.
Clinical pharmacology
A hypertonic maintenance solution whose effects reflect its water, glucose and electrolyte components. Glucose supplies energy; acetate is converted mainly in muscle and peripheral tissues to bicarbonate. Intravenous magnesium is principally eliminated in urine, making renal function important to accumulation risk.
Formulation and product differences
- Clear, particle-free solution for peripheral or central intravenous infusion in a single-use Viaflo bag.
- Contains glucose and sodium, potassium and magnesium salts, but no calcium.
- Compatibility must be established before adding another medicine; it must not share infusion equipment with whole blood.
glucose monohydrate + magnesium chloride hexahydrate + potassium chloride + sodium acetate trihydrate + sodium chloride interactions
Important interactions arise from the potassium, sodium, magnesium, glucose and alkalinising components.
ACE inhibitors and angiotensin-II receptor blockers
May increase potassium and the risk of potentially serious hyperkalaemia, particularly with renal impairment.
Potassium-sparing diuretics
Amiloride, spironolactone and triamterene may increase potassium retention and hyperkalaemia risk.
Tacrolimus or ciclosporin
Can increase plasma potassium; the combination is not recommended because severe hyperkalaemia may occur.
Sources
These sources were used to prepare and review this medicine page.
Prepared and reviewed by the iatroX editorial team.