Management of Extrapyramidal Side Effects
Extrapyramidal side effects (EPS) should be managed with specific medications based on the type of symptoms, with anticholinergic agents being the first-line treatment for acute dystonia, benztropine for parkinsonian symptoms, and beta-blockers for akathisia.
Types of Extrapyramidal Side Effects
Extrapyramidal side effects are common adverse reactions to antipsychotic medications, particularly conventional antipsychotics. They include:
- Acute dystonia: Abnormal muscle spasms and postures, usually occurring 3-5 days after starting antipsychotic therapy or increasing dosage 1
- Pseudoparkinsonism: Resembles idiopathic Parkinson's disease with tremor, rigidity, and bradykinesia, typically appearing within the first 3 months of treatment 1
- Akathisia: Characterized by subjective feelings of restlessness and anxiety with objective signs of motor activity (inability to sit still), appearing days to weeks after antipsychotic exposure 1
- Tardive dyskinesia: Late-onset involuntary movements, particularly affecting the face and mouth
Treatment Algorithm by EPS Type
1. Acute Dystonia
- First-line: Anticholinergic medications administered immediately
- Alternative: Benzodiazepines (e.g., lorazepam 0.5-2 mg) 2, 1
2. Pseudoparkinsonism
- First-line: Lower the antipsychotic dosage if clinically feasible
- Second-line: Add anticholinergic agent
- Benztropine: 1-2 mg daily, divided into 1-2 doses 2
- Third-line: Consider amantadine 100 mg twice daily
- Fourth-line: Switch to a lower-potency or atypical antipsychotic 1
3. Akathisia
- First-line: Beta-blockers
- Propranolol: 10-30 mg 2-3 times daily (use with caution in patients with asthma, diabetes, or cardiovascular disease) 2
- Second-line: Benzodiazepines (e.g., lorazepam 0.5-2 mg as needed) 2
- Third-line: Anticholinergic agents (less effective for akathisia than for other EPS) 1
- Fourth-line: Reduce antipsychotic dose or switch to an atypical antipsychotic 1
Prevention Strategies
- Use lowest effective dose of antipsychotic medication 1
- Consider atypical antipsychotics which have lower risk of EPS than conventional antipsychotics 3
- Avoid antipsychotic polytherapy as it increases risk of EPS due to higher cumulative doses 4
- Selective prophylaxis for high-risk patients:
- Young males
- First episode patients
- Previous history of EPS
- High-potency antipsychotic use 5
Important Considerations
- Do not use anticholinergic agents routinely for prophylaxis as this can add unnecessary side effect burden 5
- If prophylactic anticholinergic treatment is initiated, discontinue after approximately two weeks 5
- Long-term use of anticholinergic medications is not therapeutically beneficial and should be avoided 5
- Regular monitoring for abnormal movements using standardized scales like the Abnormal Involuntary Movement Scale (AIMS) every 3-6 months 2
- Special populations:
Common Pitfalls to Avoid
- Misdiagnosis of akathisia as anxiety or agitation, leading to inappropriate dose increases that worsen symptoms
- Prolonged anticholinergic use causing cognitive impairment, urinary retention, and constipation
- Failure to recognize EPS caused by non-antipsychotic medications (some antidepressants, lithium, anticonvulsants, antiemetics) 7
- Overlooking the emergence of tardive dyskinesia during long-term treatment
- Using doses of atypical antipsychotics higher than recommended, which increases EPS risk despite their "atypical" status 5
By following this structured approach to managing extrapyramidal side effects, clinicians can effectively reduce patient suffering and improve medication adherence while maintaining control of psychiatric symptoms.