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tardive dyskinesia

Etiology: 1) late complication of antipsychotic therapy or treatment with dopamine receptor antagonist (haloperidol, chlorpromazine, thiothixine)) a) generally noted after > 5 years of antipsychotic therapy b) isolated incidences after 1-3 months have been reported c) first generation antipsychotics with highest risk 2) anti-emetics: - metoclopramide [7] - prochlorperazine 3) antidepressants - risk associated with SSRI & tricyclic antidepressants much lower than with antipsychotics [6] - phenelzine, trazodone [7,8] 4) anticonvulsants - carbamazepine, ethosuximide, phenobarbital, phenytoin [7,8] 5) levodopa, bromocryptine [7,8] 6) amisulpride [7] 7) lithium carbonate [8] 8) estrogens [8] 9) amphetamine, methylphenidate [8] 4) longstanding psychosis 5) 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: 1) choreiform & dystonic craniofacial movements 2) rhythmic, repetitive, bizarre movements largely involving the face, mouth, jaw & tongue 3) grimacing, pursing of the lips, protrusions of the tongue, opening & closing of the mouth, & deviations of the jaw also occur 4) the extremities & trunk are less frequently involved 5) generally occurs at rest - abnormal movements lessen with activation or touch 6) the condition is often unrecognized by the patient 7) 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: - Wilson's disease - Huntington disease - brain lesion Management: 1) consider reducing or discontinuing offending antipsychotic agent - upon discontinuation of offending agent, symptoms may take months to resolve - condition may be permanent [3] - dose reduction preferable in the elderly [8] 2) switch offending antipsychotic to clozapine (Clozaril) - reduce dose of offending agent in elderly prior to switch to clozapine [8] 3) VMAT2 inhibitors a) valbenazine (Ingrezza) FDA-approved 2017 tolerated > 1 year [5] b) deutetrabenazine (Austedo) also FDA-approved 4) dose reduction preferable to VMAT2 inhibitor in the elderly [8] 5) clonazepam, 0.25-4 mg per day, is probably effective [6] 6) Gingko biloba, 80-240 mg per day, is probably effective [6] 7) amantadine is possibly effective [6]

General

dyskinesia

References

  1. Guide to Physical Examination & History Taking, 6th edition, Bates B, JB Lippincott, Philadelphia, 1995, pg 544
  2. UCLA Intensive Course in Geriatric Medicine & Board Review, Marina Del Ray, CA, Sept 12-15, 2001
  3. Medical Knowledge Self Assessment Program (MKSAP) 17, 18. American College of Physicians, Philadelphia 2015, 2018.
  4. van Harten PN, Tenback DE. Tardive dyskinesia: clinical presentation and treatment. Int Rev Neurobiol. 2011;98:187-210 PMID: 21907088
  5. 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. 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. Lutsep HL Fast Five Quiz: Movement Disorders. Medscape 2021. July 8 https://reference.medscape.com/viewarticle/954124
  8. Geriatric Review Syllabus, 11th edition (GRS11) Harper GM, Lyons WL, Potter JF (eds) American Geriatrics Society, 2022
  9. MedlinePlus Tardive dyskinesia https://medlineplus.gov/ency/article/000685.htm
  10. NINDS Tardive Dyskinesia Information Page https://www.ninds.nih.gov/Disorders/All-Disorders/Tardive-Dyskinesia-Information-Page