What is the treatment for akathisia?

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Treatment of Akathisia

The first-line treatment for akathisia is lowering the antipsychotic dose if clinically feasible, or adding propranolol 10-30 mg two to three times daily, which is the most consistently effective pharmacological intervention. 1

Initial Management Strategy

Dose reduction or medication switching should be attempted first when clinically possible, as akathisia is fundamentally a drug-induced adverse effect where prevention is superior to treatment. 1, 2

  • Reduce the current antipsychotic dosage while remaining within therapeutic range 1
  • Switch to an antipsychotic with lower akathisia risk, such as quetiapine, olanzapine, or clozapine 1, 3
  • Avoid antipsychotic polypharmacy, which increases side effect burden 1

Critical pitfall: Akathisia is frequently misinterpreted as psychotic agitation or anxiety, leading clinicians to inappropriately increase antipsychotic doses, which worsens the condition rather than improving it. 1

Pharmacological Treatment Algorithm

First-Line Pharmacotherapy: Beta-Blockers

Propranolol (10-30 mg two to three times daily) is the most consistently effective treatment based on available evidence. 1, 2, 4

  • Lipophilic beta-blockers demonstrate the strongest evidence for acute akathisia 2
  • Propranolol has limitations including orthostatic hypotension, bradycardia, contraindications in asthma, and complex titration requirements 5

Second-Line Options: When Beta-Blockers Fail or Are Contraindicated

If propranolol is unsuccessful or contraindicated, add benzodiazepines (particularly clonazepam), especially if subjective distress persists. 6, 2, 4

  • Benzodiazepines provide symptomatic relief and address the anxiety component 6, 2
  • They are part of the "B-CALM" mnemonic for akathisia management 4

Third-Line: Serotonin 5-HT2a Antagonists

Low-dose mirtazapine (7.5-15 mg once daily) has the most compelling evidence among serotonergic agents and represents an emerging treatment class. 5, 4, 7

  • Mirtazapine demonstrates strong efficacy with good tolerability 5, 4
  • Other 5-HT2a antagonists with evidence include trazodone, mianserin, and cyproheptadine 5, 3

Fourth-Line: Additional Options

If the above treatments fail, consider:

  • Amantadine (mild dopaminergic agent) 6, 2
  • Clonidine (alpha-2 agonist) 2, 4
  • Anticholinergic agents - though these are not consistently helpful for akathisia specifically and are more effective for other extrapyramidal symptoms 6, 2
  • Gabapentin or pregabalin (voltage-gated calcium channel blockers) 4, 7

Important caveat: Anticholinergic agents are notably less effective for akathisia compared to other extrapyramidal side effects like dystonia or parkinsonism, despite being commonly prescribed. 6, 2

Special Populations and Considerations

Children and Adolescents

  • Children and adolescents may be at higher risk for extrapyramidal side effects, including akathisia, compared to adults 6
  • Monitor carefully for anticholinergic side effects when using anticholinergic agents 1

Acute Emergency Settings

  • Intramuscular administration is preferred over intravenous route for acute akathisia management 1

Cardiovascular Risk Patients

  • Carefully consider QT-prolonging effects when switching antipsychotics in patients with high cardiovascular risk 1

Chronic and Tardive Akathisia

Evidence for treating tardive akathisia is unsatisfactory and these cases may prove resistant to standard pharmacological interventions. 2, 7

  • Chronic akathisia may persist even after discontinuing the causative agent 7
  • Rotation between different pharmacological management strategies may be optimal in resistant cases 7
  • Discontinuation of the causative drug remains the foundation of management 7

References

Guideline

Treatment Options for Akathisia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

[Drug-induced akathisia].

Nederlands tijdschrift voor geneeskunde, 2002

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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