Drug Guide

Generic Name

Pancuronium Bromide

Brand Names Pavulon

Classification

Therapeutic: Neuromuscular Blocking Agent

Pharmacological: Non-depolarizing Muscle Relaxant

FDA Approved Indications

  • Adjunct to general anesthesia to facilitate endotracheal intubation and provide skeletal muscle relaxation during surgery or mechanical ventilation.

Mechanism of Action

Pancuronium Bromide is a non-depolarizing neuromuscular blocker that antagonizes acetylcholine at the neuromuscular junction, preventing depolarization and leading to muscle paralysis.

Dosage and Administration

Adult: Иnitial dose of 0.08 to 0.1 mg/kg IV, with additional doses of 0.02 mg/kg as needed. Maintenance dosages depend on clinical response.

Pediatric: Dose varies; typically 0.04 to 0.1 mg/kg IV, with supplementary doses based on response.

Geriatric: Reduced doses may be necessary, starting at lower end of dosing range.

Renal Impairment: Adjust doses as accumulation may occur due to impaired excretion.

Hepatic Impairment: No specific adjustments; monitor closely.

Pharmacokinetics

Absorption: Not applicable (administered IV).

Distribution: Widely distributed; crosses the placenta.

Metabolism: Primarily excreted unchanged; minimal metabolism.

Excretion: Renal and biliary routes.

Half Life: Approximately 2-3 hours in healthy individuals, prolonged in renal impairment.

Contraindications

  • Known hypersensitivity to pancuronium or other neuromuscular blockers.

Precautions

  • Use with caution in myasthenia gravis, hepatic or renal impairment, or severe electrolyte imbalances. Monitor closely in these populations.

Adverse Reactions - Common

  • Prolonged paralysis (Rare)
  • Tachycardia (Common)
  • Hypotension or hypertension (Uncommon)

Adverse Reactions - Serious

  • Anaphylaxis (Rare)
  • Malignant hyperthermia (less common) (Rare)

Drug-Drug Interactions

  • Increased neuromuscular blockade with other neuromuscular blockers or aminoglycosides.
  • Decreased blockade effect with cholinesterase inhibitors.

Drug-Food Interactions

N/A

Drug-Herb Interactions

N/A

Nursing Implications

Assessment: Monitor ventilatory status, neuromuscular function (e.g., peripheral nerve stimulator), and vital signs.

Diagnoses:

  • Risk for impaired gas exchange.
  • Impaired airway clearance.

Implementation: Administer dosage as prescribed, monitor for adequate paralysis and recovery, and provide appropriate ventilatory support.

Evaluation: Assess neuromuscular function regularly; ensure patient has resumed adequate spontaneous respirations and muscle strength.

Patient/Family Teaching

  • Explain the purpose of muscle paralysis and ventilatory support.
  • Inform about possible side effects and signs to report.
  • Reassure that paralysis is reversible and monitored closely.

Special Considerations

Black Box Warnings:

  • Use with caution in patients with known hypersensitivity; potential for prolonged paralysis.

Genetic Factors: N/A

Lab Test Interference: N/A

Overdose Management

Signs/Symptoms: Complete paralysis, respiratory depression, circulatory collapse.

Treatment: Provide supportive care, including mechanical ventilation; consider administration of cholinesterase inhibitors (e.g., neostigmine) to reverse paralysis if appropriate.

Storage and Handling

Storage: Store in a cool, dry place, protected from light.

Stability: Stable under recommended storage conditions.

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