Tardive Dyskinesia: Understanding and Management
Tardive dyskinesia is an involuntary movement disorder characterized by repetitive, purposeless movements primarily affecting the face and extremities, caused by long-term use of antipsychotic medications, which should be treated with VMAT2 inhibitors (valbenazine or deutetrabenazine) when moderate to severe. 1
What is Tardive Dyskinesia?
Tardive dyskinesia (TD) is a medication-induced movement disorder that develops after prolonged exposure to dopamine receptor blocking agents, primarily antipsychotic medications. The condition is characterized by:
- Orofacial movements: Repetitive tongue movements, tongue protrusion, chewing movements, facial grimacing, excessive blinking, and lip puckering 1
- Extremity movements: Choreic (rapid, irregular) movements of fingers and hands, athetoid (slow, contorted) movements of limbs 1
- Other manifestations: Can present as dystonia (most common), chorea, or rarely ballism 1
Most TD episodes last less than 1 minute in over 98% of patients 1.
Risk Factors
Understanding who is at risk helps with prevention and early detection:
- Duration of treatment: Risk increases with longer exposure to antipsychotics 1
- Cumulative dose: Higher total doses increase risk 1
- Age: Elderly patients have up to 50% risk after 2 years of continuous typical antipsychotic use 1
- Gender: Women are at higher risk 1
- Pre-existing conditions: Intellectual impairment increases risk 1
- Medication type: Higher risk with first-generation (typical) antipsychotics than second-generation (atypical) antipsychotics 2
Diagnosis
TD must be differentiated from other movement disorders as treatments differ:
- Drug-induced parkinsonism: Characterized by rigidity, bradykinesia, and tremor
- Akathisia: Motor restlessness and inability to sit still
- Withdrawal dyskinesia: Similar movements that occur after stopping antipsychotics but typically resolve 3
Management Approach
1. Prevention is Primary
- Use antipsychotics only when clinically indicated
- Prescribe minimum effective doses
- Regularly monitor using Abnormal Involuntary Movement Scale (AIMS) every 3-6 months
- Record baseline abnormal movements before starting antipsychotics 1
2. First-line Management
- Discontinue antipsychotic if clinically feasible 2
- However, for many patients with serious mental illness, discontinuation may not be possible due to risk of relapse
- If discontinuation is not possible, consider switching to an antipsychotic with lower TD risk (e.g., clozapine or quetiapine) 2
3. Pharmacological Treatment
For moderate to severe or disabling TD:
- VMAT2 inhibitors (first-line pharmacological treatment) 1:
Valbenazine (Ingrezza): FDA-approved for TD
- Starting dose: 40 mg daily
- Target dose: 80 mg daily
- Advantages: Once-daily dosing, rapid onset (within 2 weeks)
Deutetrabenazine (Austedo): FDA-approved for TD
- Effective dose: 24-36 mg/day
- Administration: Twice-daily with food
- Requires gradual titration to minimize side effects
Both medications have demonstrated significant reduction in TD symptoms with response rates of 33-50% 1.
4. Alternative Treatments (when VMAT2 inhibitors are unavailable or not tolerated)
- Amantadine
- Clonazepam
- Ginkgo biloba
- Beta-blockers 1
Note: Anticholinergics (benztropine, trihexyphenidyl) should be avoided as they may worsen TD symptoms 1.
5. For Severe Refractory Cases
- Electroconvulsive therapy (ECT) may be considered when medications are ineffective 1
Special Considerations
- Elderly patients: Higher risk for TD; require careful monitoring and lower doses 1
- Hepatic impairment: May contraindicate certain medications like deutetrabenazine 1
- Patients with mood disorders: Balance TD risk against risk of mood disorder relapse 1
Prognosis
TD can be irreversible in some cases, but early intervention improves outcomes:
- TD may remit partially or completely if antipsychotic treatment is withdrawn early 3
- The risk of irreversibility increases with longer duration of symptoms 1
- Early detection and intervention are crucial for better outcomes 4
Understanding tardive dyskinesia and implementing appropriate prevention and management strategies are essential for improving outcomes in patients requiring long-term antipsychotic treatment.