tardive dyskinesia
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Etiology
- late complication of antipsychotic therapy or treatment with dopamine receptor antagonist (haloperidol, chlorpromazine, thiothixine))
- generally noted after > 5 years of antipsychotic therapy
- isolated incidences after 1-3 months have been reported
- first generation antipsychotics with highest risk
- anti-emetics:
- antidepressants
- risk associated with SSRI & tricyclic antidepressants much lower than with antipsychotics[6]
- phenelzine, trazodone[7][8]
- anticonvulsants
- levodopa, bromocryptine[7][8]
- amisulpride[7]
- lithium carbonate[8]
- estrogens[8]
- amphetamine, methylphenidate[8]
- longstanding psychosis
- idiopathic on some elderly individuals, especially if edentulous
Epidemiology
- may be 20-30% with long-term use of antipsychotic
Pathology
- dopamine receptor sensitivity in the basal ganglia
Clinical manifestations
- choreiform & dystonic craniofacial movements
- rhythmic, repetitive, bizarre movements largely involving the face, mouth, jaw & tongue
- grimacing, pursing of the lips, protrusions of the tongue, opening & closing of the mouth, & deviations of the jaw also occur
- the extremities & trunk are less frequently involved
- generally occurs at rest
- abnormal movements lessen with activation or touch
- the condition is often unrecognized by the patient
- symptoms may take months to resolve of become permanent.
Diagnostic criteria
- neuroleptic-induced tardive dyskinea requires symptoms that persist for 1 month after exposure to neuroleptics for >= 3 months
- at least 1 month of exposure is required if patient is > 60 years[7]
Differential diagnosis
Management
- consider reducing or discontinuing offending antipsychotic agent
- switch offending antipsychotic to clozapine (Clozaril)
- VMAT2 inhibitors
- valbenazine (Ingrezza) FDA-approved 2017 tolerated > 1 year[5]
- deutetrabenazine (Austedo) also FDA-approved
- dose reduction preferable to VMAT2 inhibitor in the elderly[8]
- clonazepam, 0.25-4 mg per day, is probably effective[6]
- Gingko biloba, 80-240 mg per day, is probably effective[6]
- amantadine is possibly effective[6]
More general terms
References
- ↑ Guide to Physical Examination & History Taking, 6th edition, Bates B, JB Lippincott, Philadelphia, 1995, pg 544
- ↑ UCLA Intensive Course in Geriatric Medicine & Board Review, Marina Del Ray, CA, Sept 12-15, 2001
- ↑ 3.0 3.1 Medical Knowledge Self Assessment Program (MKSAP) 17, 18. American College of Physicians, Philadelphia 2015, 2018.
- ↑ van Harten PN, Tenback DE. Tardive dyskinesia: clinical presentation and treatment. Int Rev Neurobiol. 2011;98:187-210 PMID: https://www.ncbi.nlm.nih.gov/pubmed/21907088
- ↑ 5.0 5.1 Visk D Valbenazine for Tardive Dyskinesia Tolerated Long-Term - Only 15% of patients discontinued tx over 1 year due to adverse events. MedPage Today. May 28, 2017 https://www.medpagetoday.com/MeetingCoverage/APA/65645
Josiassen RC, et al Long-term safety and tolerability of valbenazine in subjects with tardive dyskinesia and a diagnosis of schizophrenia or mood disorders. American Psychiatric Association (APA) 2017. - ↑ 6.0 6.1 6.2 6.3 6.4 Swan M Fast Five Quiz: How Much Do You Know About Tardive Dyskinesia? Medscape 2021. May 21 https://reference.medscape.com/viewarticle/910550_2
- ↑ 7.0 7.1 7.2 7.3 7.4 7.5 7.6 Lutsep HL Fast Five Quiz: Movement Disorders. Medscape 2021. July 8 https://reference.medscape.com/viewarticle/954124
- ↑ 8.0 8.1 8.2 8.3 8.4 8.5 8.6 8.7 8.8 8.9 Geriatric Review Syllabus, 11th edition (GRS11) Harper GM, Lyons WL, Potter JF (eds) American Geriatrics Society, 2022
- ↑ MedlinePlus Tardive dyskinesia https://medlineplus.gov/ency/article/000685.htm
- ↑ NINDS Tardive Dyskinesia Information Page https://www.ninds.nih.gov/Disorders/All-Disorders/Tardive-Dyskinesia-Information-Page