Drug Guide

Generic Name

Calcium Chloride, Dextrose, Magnesium Chloride, Potassium Chloride, Sodium Acetate, Sodium Chloride, Sodium Lactate (Plasma-Lyte M and Dextrose 5%)

Brand Names Plasma-Lyte M, Dextrose 5% in Plastic Container

Classification

Therapeutic: Electrolyte and fluid replacement solution

Pharmacological: Intravenous electrolyte and fluid therapy

FDA Approved Indications

  • Electrolyte replenishment
  • Fluid replacement in dehydration
  • Correction of metabolic acidosis

Mechanism of Action

Provides essential electrolytes and buffers to restore fluid and electrolyte balance and maintain blood pH.

Dosage and Administration

Adult: Dosage varies based on clinical condition; administer via infusion, titrated based on electrolyte levels and fluid status.

Pediatric: Dose determined based on body weight and clinical condition, under medical supervision.

Geriatric: Same as adult, with attention to renal function and electrolyte levels.

Renal Impairment: Adjust dosages based on severity of renal impairment; monitor electrolytes closely.

Hepatic Impairment: Use with caution; monitor for acid-base and electrolyte disturbances.

Pharmacokinetics

Absorption: N/A (intravenous administration)

Distribution: Electrolytes distribute throughout body compartments; plasma concentrations reflect extracellular fluid levels.

Metabolism: Electrolytes are not metabolized but used in cellular and metabolic functions.

Excretion: Electrolytes are eliminated via renal and gastrointestinal routes.

Half Life: Varies depending on electrolyte and fluid status; primarily renal clearance.

Contraindications

  • Hyperkalemia
  • Hypernatremia
  • Hypercalcemia
  • Severe renal impairment
  • Acidosis

Precautions

  • Monitor serum electrolyte levels regularly during therapy
  • Use with caution in cardiac disease, kidney dysfunction, or edema
  • Avoid rapid infusion to prevent cardiovascular or metabolic complications

Adverse Reactions - Common

  • Hypokalemia (rare)
  • Hyperkalemia (rare)
  • Fluid overload or edema (rare)
  • Hypernatremia (rare)
  • Local irritation at infusion site (rare)

Adverse Reactions - Serious

  • Cardiac arrhythmias (rare)
  • Metabolic acidosis/alkalosis depending on electrolyte imbalance (rare)

Drug-Drug Interactions

  • Potassium-sparing diuretics, ACE inhibitors (risk of hyperkalemia)
  • Digoxin (risk of toxicity with electrolyte imbalance)

Drug-Food Interactions

N/A

Drug-Herb Interactions

N/A

Nursing Implications

Assessment: Monitor serum electrolytes, renal function, hydration status, and cardiac rhythm.

Diagnoses:

  • Risk for electrolyte imbalance
  • Fluid volume excess

Implementation: Administer IV solutions per ordered rate, monitor infusion site, observe for adverse effects.

Evaluation: Assess for resolution of electrolyte imbalances, hydration status, and absence of adverse reactions.

Patient/Family Teaching

  • Report any swelling, chest pain, irregular heartbeat, or changes in mental status.
  • Avoid other sources of excess electrolytes without healthcare provider guidance.

Special Considerations

Black Box Warnings: N/A

Genetic Factors: Genetic conditions affecting electrolyte handling are not specifically impacted by these solutions.

Lab Test Interference: Electrolyte solutions can affect serum electrolyte measurements; draw labs before infusion if possible.

Overdose Management

Signs/Symptoms: Hyperkalemia, hypernatremia, fluid overload, cardiac arrhythmias.

Treatment: Discontinue infusion, correct electrolytes with specific antidotes if needed, provide supportive care, consider dialysis in severe cases.

Storage and Handling

Storage: Store at controlled room temperature, away from light and moisture.

Stability: Stable until expiration if stored properly; consult manufacturer guidelines.

This guide is for educational purposes only and is not intended for clinical use.