Drug Guide
Pancuronium Bromide
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/ADrug-Herb Interactions
N/ANursing 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.