What medications should be stopped before Electroconvulsive Therapy (ECT)?

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Last updated: November 26, 2025View editorial policy

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Medications to Discontinue Before ECT

The following medications should be discontinued prior to ECT: lithium, benzodiazepines, carbamazepine, theophylline, and trazodone, as these pose the highest risk for serious complications including acute brain syndrome, seizure induction failure, and prolonged seizures. 1, 2

High-Priority Medications Requiring Discontinuation

Lithium

  • Must be discontinued when clinically possible due to reports of acute brain syndrome and delirium when used concurrently with ECT 1, 3
  • Lithium combined with ECT adds significant risk of organic syndromes developing 3

Anticonvulsants

  • Carbamazepine should be stopped as it has been associated with failure to induce seizures during ECT and may prolong the action of succinylcholine 1, 3
  • Valproate, lamotrigine, gabapentin, and topiramate may inhibit seizure activity and should be carefully considered for discontinuation 3, 4
  • Recent evidence suggests anticonvulsants may be a relative rather than absolute contraindication, but require careful risk-benefit assessment 4

Benzodiazepines

  • Should be discontinued as they increase seizure threshold through anticonvulsant properties, potentially making it difficult to induce therapeutic seizures 1, 2, 3
  • Their anticonvulsant effects may interfere with the therapeutic efficacy of ECT 3

Other High-Risk Medications

  • Theophylline must be stopped as it prolongs seizure duration at both therapeutic and toxic levels 1, 2
  • Trazodone should be discontinued due to reported adverse effects, specifically prolonged seizures during ECT 1, 2

Medications That Can Be Continued

Antidepressants

  • Tricyclic antidepressants (TCAs) can be safely continued and may actually enhance ECT efficacy 3, 5
  • Nortriptyline specifically enhances ECT efficacy and reduces cognitive adverse effects compared to placebo 5
  • SSRIs do not significantly affect seizure duration (31.4 seconds vs 33.2 seconds with TCAs) and can be continued 6
  • Venlafaxine resulted in weaker improvement and tended to worsen cognitive adverse effects, requiring more caution 5

Antipsychotics and Other Medications

  • Antipsychotics are well tolerated with ECT and may be beneficial 3
  • Olanzapine and mirtazapine can be continued as part of maintenance treatment strategy 2

Critical Management Considerations

Timing and Monitoring

  • Monitor patients for at least 24 hours after ECT for tardive seizures (late-onset seizures occurring after full recovery from anesthesia) 7, 1
  • Prolonged seizures (>180 seconds) occur in 0-10% of treatments and require termination with additional methohexital, diazepam, or lorazepam 7, 1

When Discontinuation Is Not Possible

  • If medications cannot be discontinued due to clinical necessity, they may be administered with appropriate monitoring 1
  • Obtain neurology consultation if recurrent prolonged seizures or tardive seizures occur 7, 1

Common Pitfalls to Avoid

  • Do not use MAOIs carelessly with ECT, especially older irreversible varieties and in patients recently started on MAOI therapy 3
  • Avoid calcium channel antagonists or use with great care to prevent significant cardiovascular depression 3
  • CNS stimulants may prolong seizures and produce dysrhythmias and elevated blood pressure 3

Post-ECT Medication Restart

  • Medications can typically be restarted after completing the ECT course based on clinical need 1
  • Pharmacotherapy and/or maintenance treatment should be initiated after the last ECT treatment, as ECT does not prevent future relapse 7

References

Guideline

Medications to Discontinue Prior to Electroconvulsive Therapy (ECT)

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Medication Management During Electroconvulsive Therapy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Effects of antidepressant treatments on first-ECT seizure duration in depression.

Progress in neuro-psychopharmacology & biological psychiatry, 2001

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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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