Atracurium Dosing for Induction and Maintenance of Neuromuscular Blockade
For induction of neuromuscular blockade, atracurium should be administered at 0.4-0.5 mg/kg IV bolus, followed by maintenance doses of 0.08-0.10 mg/kg every 20-45 minutes as needed based on train-of-four monitoring. 1
Induction Dosing
The FDA-approved dosing for atracurium provides clear guidance:
Standard induction dose: 0.4-0.5 mg/kg IV bolus 1
- This dose is 1.7-2.2 times the ED95 (effective dose for 95% neuromuscular blockade)
- Provides good to excellent intubation conditions within 2-2.5 minutes
- Maximum blockade occurs approximately 3-5 minutes after injection
- Clinical duration of action is typically 20-35 minutes under balanced anesthesia
Special populations:
Anesthetic considerations:
Maintenance Dosing
Intermittent bolus dosing: 0.08-0.10 mg/kg IV 1
- First maintenance dose typically required 20-45 minutes after initial injection
- Subsequent doses needed approximately every 15-25 minutes under balanced anesthesia
- Slightly longer intervals under isoflurane or enflurane
- Higher maintenance doses (up to 0.2 mg/kg) allow for longer dosing intervals 1
Continuous infusion:
Monitoring and Administration Considerations
- Use peripheral nerve stimulation (train-of-four monitoring) to guide dosing and prevent overdosage or underdosage 1
- Do not administer before unconsciousness has been induced 1
- Do not mix with alkaline solutions (e.g., barbiturate solutions) in the same syringe 1
- Administer intravenously only; intramuscular administration is not recommended 1
Clinical Pharmacology Considerations
- Atracurium is an intermediate-acting neuromuscular blocking agent 3
- Metabolism occurs via ester hydrolysis and Hofmann elimination, independent of renal or hepatic function 3, 4
- Recovery to 25% of control typically occurs 35-45 minutes after injection 1
- Recovery is usually 95% complete approximately 60 minutes after injection 1
- Minimal cardiovascular effects at standard doses, though higher doses (>0.5 mg/kg) may cause histamine release 3, 4
- Laudanosine, a breakdown product, has been associated with CNS excitation with extremely high doses or in hepatic failure 3
Cautions and Pitfalls
- Histamine release can occur at higher doses, potentially causing cardiovascular effects 3
- Always ensure adequate sedation and analgesia before administration 1
- For rapid sequence induction, higher doses (0.75-1.0 mg/kg) may be required but increase the risk of histamine-related side effects 5
- Avoid cumulative effects by using appropriate monitoring to guide dosing intervals 4
- Consider cisatracurium as an alternative when histamine release is a concern, as it has minimal cardiovascular effects and less tendency for mast cell degranulation 3, 6