Drug Guide
Atracurium Besylate
Classification
Therapeutic: Skeletal muscle relaxant, non-depolarizing
Pharmacological: Nm-blocker (neuromuscular blocker)
FDA Approved Indications
- Facilitation of endotracheal intubation during anesthesia
- Muscle relaxation during surgery
Mechanism of Action
Atracurium binds competitively to acetylcholine receptors at the neuromuscular junction, preventing acetylcholine from activating these receptors, leading to muscle relaxation. It undergoes Hoffmann elimination, which is independent of organ function.
Dosage and Administration
Adult: Dose varies based on procedure; typically 0.4-0.5 mg/kg IV for intubation, followed by additional doses as needed.
Pediatric: Dosing similar to adults; specific pediatric dosing depends on weight and clinical situation.
Geriatric: Start with lower doses; monitor closely due to increased sensitivity.
Renal Impairment: Use with caution; dose adjustments may be necessary.
Hepatic Impairment: Use with caution; however, no specific adjustments are usually required due to organ-independent metabolism.
Pharmacokinetics
Absorption: Administered IV, not absorbed via other routes.
Distribution: Widely distributed in body tissues and fluids.
Metabolism: Undergoes Hoffmann elimination and ester hydrolysis; organ-independent.
Excretion: Primarily eliminated via plasma esterases and Hoffman elimination.
Half Life: 20-35 minutes in adults, varies with dose and patient condition.
Contraindications
- Known hypersensitivity to atracurium or other components.
- History of histamine release reactions.
Precautions
- Use cautiously in patients with cardiovascular disease, as histamine release can cause hypotension and bronchospasm.
- Monitor for signs of allergic reactions or significant hypotension.
Adverse Reactions - Common
- Histamine release leading to flushing, hypotension, bronchospasm (Occasional)
- Muscle pain or weakness postoperatively (Rare)
Adverse Reactions - Serious
- Anaphylaxis (Rare)
- Prolonged paralysis (Rare)
Drug-Drug Interactions
- Other neuromuscular blockers (additive effects), aminoglycoside antibiotics, magnesium sulfate, calcium channel blockers
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor neuromuscular function (e.g., Train-of-Four), vital signs, and oxygen saturation.
Diagnoses:
- Impaired gas exchange
- Risk for ineffective airway clearance
- Impaired physical mobility
Implementation: Administer IV carefully, monitor patient response, and have resuscitation equipment available.
Evaluation: Assess muscle strength and respiratory status to determine adequacy of paralysis and recovery.
Patient/Family Teaching
- Inform about potential muscle weakness and breathing difficulties.
- Report signs of allergic reactions, such as rash, difficulty breathing.
- Assure about the temporary nature of muscle relaxation.
Special Considerations
Black Box Warnings:
- None specific for atracurium.
Genetic Factors: Genetic variations in plasma cholinesterase can affect metabolism of other agents, but not atracurium.
Lab Test Interference: None known.
Overdose Management
Signs/Symptoms: Persistent paralysis, difficulty breathing, cyanosis.
Treatment: Supportive care with mechanical ventilation, monitor neuromuscular function, may administer cholinesterase inhibitors (e.g., neostigmine) to reverse effects if appropriate.
Storage and Handling
Storage: Store at room temperature, protected from moisture.
Stability: Stable under recommended storage conditions for the labeled shelf life.