Atracurium Dosing in Obese Patients
Atracurium should be dosed based on ideal body weight (IBW), not total body weight, in obese patients to ensure predictable neuromuscular blockade with appropriate recovery times and minimal need for reversal agents. 1, 2
Recommended Dosing Strategy
Initial Intubating Dose
- Administer atracurium 0.5 mg/kg based on ideal body weight for the initial intubating dose in obese patients 2
- This dosing provides adequate intubation conditions within 2-2.5 minutes and allows recovery of muscle strength to a train-of-four (TOF) ratio >90% within 60 minutes without requiring reversal 2
- The standard initial dose range of 0.4-0.5 mg/kg applies, but the weight used for calculation must be IBW, not total body weight 3, 2
Maintenance Dosing
- Use 0.08-0.10 mg/kg based on ideal body weight for maintenance doses during prolonged procedures 3
- First maintenance dose typically required 20-45 minutes after initial dose, with subsequent doses at approximately 15-25 minute intervals 3
Continuous Infusion
- Initial infusion rate: 9-10 mcg/kg/min based on ideal body weight, then reduce to 5-9 mcg/kg/min for maintenance 3
- Adjust rate based on peripheral nerve stimulation monitoring to maintain 89-99% neuromuscular blockade 3
Rationale for Ideal Body Weight Dosing
Evidence from Clinical Studies
- Dosing based on total body weight causes dose-dependent prolongation of neuromuscular blockade with significantly longer and more variable recovery times 2, 4
- In patients weighing 112-260 kg, total body weight dosing resulted in 70% requiring neostigmine reversal at surgery end, compared to 0% with IBW dosing 2
- The time to recovery of TOF ratio from 0 to 5% was 30 minutes shorter (95% CI: 23-39 minutes) when using IBW versus total body weight 2
Pharmacokinetic Considerations
- Atracurium undergoes organ-independent elimination via Hofmann degradation and ester hydrolysis, making it particularly suitable for obese patients 5, 3
- Despite organ-independent metabolism, total body weight dosing still results in relative overdosing because excess adipose tissue has low blood flow and limited drug distribution 1, 4
- Duration of action correlates significantly with total body weight (r² = 0.264, P < 0.0001), confirming the need for dose reduction in obesity 4
Special Considerations in Obesity with Organ Dysfunction
Renal or Hepatic Impairment
- Do not modify the initial atracurium dose in patients with renal or hepatic failure, regardless of obesity status 5
- Atracurium's pharmacokinetics and pharmacodynamics remain similar in patients with and without kidney and liver failure 5
- The active metabolite laudanosine may accumulate in renal failure but does not reach toxic concentrations even after 72-hour infusions 5
- Atracurium is the preferred neuromuscular blocking agent when both obesity and renal/hepatic failure coexist 5
Dosing Algorithm for Obese Patients with Organ Dysfunction
- Calculate ideal body weight using standard formulas based on height and sex 1
- Administer standard atracurium dose (0.4-0.5 mg/kg) based on IBW - do not reduce dose for renal or hepatic impairment 5
- Monitor neuromuscular blockade with train-of-four stimulation at the adductor pollicis 5, 2
- Adjust maintenance dosing or infusion rates based on TOF monitoring, not weight-based calculations alone 3, 2
Monitoring and Reversal
Neuromuscular Monitoring
- Train-of-four monitoring is essential to assess degree of muscle relaxation and guide dosing 3, 2
- Target TOF ratio >0.9 before extubation to ensure adequate reversal 5
Reversal with Neostigmine
- Administer neostigmine 40-50 mcg/kg based on ideal body weight when reversal is needed 5
- Do not exceed this dose range due to ceiling effect and potential adverse effects on airway patency 5
- Reversal should only be attempted when some spontaneous recovery has begun (at least 1-2 twitches present on TOF) 5, 3
- Complete reversal typically achieved within 8-10 minutes of neostigmine administration 3
Common Pitfalls to Avoid
Dosing Errors
- Never dose atracurium based on total body weight in obese patients - this leads to prolonged blockade requiring reversal in 70% of cases 2
- Avoid the outdated recommendation to reduce dose by 0.23 mg for each kg above 70 kg total body weight - simply use IBW instead 4
- Do not reduce the initial dose in renal or hepatic failure, as onset time and initial efficacy remain unchanged 5
Cardiovascular Considerations
- Use reduced initial doses (0.3-0.4 mg/kg IBW) given slowly over one minute in patients with significant cardiovascular disease or history of severe anaphylactoid reactions 3
- Doses up to 0.5 mg/kg produce minimal histamine release, but 0.6 mg/kg may cause moderate histamine release and blood pressure falls 3