Which medication is used in electroconvulsive therapy to minimize violent muscle contractions?

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Muscle Relaxant for ECT

Succinylcholine at a dose of 0.9 mg/kg IV is the standard muscle relaxant used in electroconvulsive therapy to minimize violent muscle contractions. 1

Primary Recommendation

The American Academy of Child and Adolescent Psychiatry establishes succinylcholine as the standard muscle relaxant for ECT, with acceptable alternatives including atracurium and mivacurium. 1 This recommendation is based on succinylcholine's rapid onset, short duration of action, and predictable muscle relaxation profile during induced seizures.

Dosing Strategy

  • The standard dose of succinylcholine is 0.9 mg/kg IV, though research demonstrates the minimum effective dose ranges from 0.77-1.27 mg/kg to produce acceptable muscle blockade in 50-90% of patients. 1, 2

  • The dose should be selected based on each patient's preprocedural condition, with higher doses (approaching 1.27 mg/kg) needed for more robust patients or when greater muscle control is required. 2

  • A twitch suppression of >90% is necessary for adequate control of motor contractions during ECT. 2

Alternative Muscle Relaxants

Rocuronium as an Alternative

  • Rocuronium (0.36-0.6 mg/kg) combined with neostigmine reversal is a safe alternative when succinylcholine is contraindicated or undesirable. 2

  • When using rocuronium, the minimum effective dose ranges from 0.36-0.46 mg/kg for 50% of patients and 0.5-0.6 mg/kg for 90% of patients. 2

  • Rocuronium with sugammadex reversal (8 mg/kg) produces equally rapid recovery compared to spontaneous recovery from succinylcholine, making it a viable option. 3

  • The American Society of Anesthesiologists recommends rocuronium can be safely used in patients with seizure disorders when combined with sugammadex for reversal, as it does not lower the seizure threshold. 4

Mivacurium Limitations

  • Low-dose mivacurium (0.08 mg/kg) is unsuitable for ECT as it provides inadequate seizure modification compared to succinylcholine. 5

  • Research shows mivacurium was unsatisfactory in 50% of cases (8 out of 16 patients), leading to early study termination due to poor seizure control. 5

  • However, mivacurium may be considered in special circumstances such as patients with neuroleptic malignant syndrome where succinylcholine should be avoided due to malignant hyperthermia concerns. 6

Clinical Considerations and Monitoring

  • Neuromuscular monitoring is essential when using any muscle relaxant to ensure adequate blockade and complete recovery before patient discharge. 4, 2

  • Recovery time from succinylcholine averages 9.7 ± 3.5 minutes, while rocuronium with neostigmine reversal takes approximately 19.5 ± 5.7 minutes. 2

  • For rocuronium reversal, sugammadex dosing depends on depth of blockade: 2.0 mg/kg for moderate, 4.0 mg/kg for deep, or 8.0 mg/kg for very deep blockade. 4

Important Caveats

  • Avoid succinylcholine in patients with neuroleptic malignant syndrome due to potential cross-reactivity with malignant hyperthermia triggers; use mivacurium or rocuronium instead. 6

  • In obese patients, non-depolarizing muscle relaxants (rocuronium, atracurium, mivacurium) should be dosed based on lean body weight rather than actual body weight. 4

  • The efficacy of sugammadex for rocuronium reversal may be decreased in elderly patients and those with severe renal failure, requiring dose adjustments and careful monitoring. 4

References

Guideline

Anesthetic Regimens for ECT Sessions

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Muscle Relaxants in Patients with Seizure Disorders

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Low dose mivacurium is less effective than succinylcholine in electroconvulsive therapy.

Canadian journal of anaesthesia = Journal canadien d'anesthesie, 1999

Research

Neuroleptic malignant syndrome and mivacurium: a safe alternative to succinylcholine?

Canadian journal of anaesthesia = Journal canadien d'anesthesie, 1994

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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