Drug Guide
Magnesium Sulfate, Potassium Chloride, Potassium Phosphate Monobasic, Sodium Chloride, Sodium Phosphate (Tis-u-sol)
Classification
Therapeutic: Electrolyte replacement and fluid therapy
Pharmacological: Electrolytes and salts
FDA Approved Indications
- Electrolyte replenishment in deficiency states
- Fluid and electrolyte maintenance during surgery or critical illness
Mechanism of Action
Provides essential electrolytes that participate in numerous physiological processes, including nerve conduction, muscle contraction, and osmotic balance.
Dosage and Administration
Adult: Dosing varies based on clinical need; typically administered intravenously under medical supervision.
Pediatric: Dosing adjusted based on age, weight, and clinical condition; administered under supervision.
Geriatric: Cautious use due to risk of electrolyte imbalance; monitor levels closely.
Renal Impairment: Use with caution; adjust doses according to electrolyte levels and renal function.
Hepatic Impairment: No specific adjustments generally required.
Pharmacokinetics
Absorption: IV administration ensures direct entry into bloodstream.
Distribution: Widely distributed in body fluids.
Metabolism: Not metabolized; excreted unchanged.
Excretion: Primarily renal excretion.
Half Life: Varies; magnesium and potassium have half-lives of approximately 4-6 hours, depending on renal function.
Contraindications
- Hypermagnesemia, Hyperkalemia, Renal failure, Severe dehydration
Precautions
- Use cautiously in patients with cardiac disease, hepatic impairment, or electrolyte disturbances. Close monitoring required.
Adverse Reactions - Common
- Vasodilation leading to hypotension (Uncommon)
- Flushing, feeling of warmth (Common)
Adverse Reactions - Serious
- Arrhythmias, Cardiac arrest (with severe hyperkalemia or hypermagnesemia) (Rare)
Drug-Drug Interactions
- Potentiates effects of other neuromuscular blocking agents
- Increases risk of hyperkalemia with certain medications
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor electrolytes, renal function, cardiac status, and vital signs.
Diagnoses:
- Risk for electrolyte imbalance
- Risk for impaired cardiac output
Implementation: Administer cautiously, monitor serum levels, and adjust dosing accordingly.
Evaluation: Electrolyte levels within normal range, stable cardiac status, absence of adverse reactions.
Patient/Family Teaching
- Report signs of irregular heartbeat, weakness, or swelling.
- Understand the importance of laboratory monitoring and follow-up.
- Adherence to prescribed dosing and instructions.
Special Considerations
Black Box Warnings:
- Administer cautiously to avoid toxicity, especially in renal impairment.
Genetic Factors: No specific genetic considerations known.
Lab Test Interference: May alter serum magnesium, potassium, phosphate, and sodium measurements.
Overdose Management
Signs/Symptoms: Signs of hypermagnesemia (muscle weakness, decreased reflexes, respiratory depression), hyperkalemia (muscle weakness, arrhythmias).
Treatment: Discontinuation of infusion, supportive care, calcium gluconate for magnesium toxicity, sodium bicarbonate or insulin plus glucose for hyperkalemia.
Storage and Handling
Storage: Store at room temperature, protected from moisture.
Stability: Stable under recommended storage conditions.