American Psychiatric Association (APA) guideline recommendations: VMAT2 inhibitor as first-line treatment for tardive dyskinesia (TD)1,2

American Academy of Neurology (AAN): VMAT2 inhibitor class is backed by the highest level of therapeutic evidence, regardless of severity2*

Table level of evidence for tardive dyskinesia (TD) treatments, VMAT2 inhibitor, ginkgo biloba, tetrabenazine, and pallidal deep brain stimulation Table level of evidence for tardive dyskinesia (TD) treatments, VMAT2 inhibitor, ginkgo biloba, tetrabenazine, and pallidal deep brain stimulation
  • APA guidelines recommend starting a VMAT2 inhibitor to address TD-associated impairments and impact on psychosocial functioning1
  • Update to AAN guidelines recognizes VMAT2 inhibitors as first-line treatment for TD2

*

Level A is the strongest recommendation, established as effective, based on at least 2 consistent class I studies. Level B refers to probably effective treatment, derived from at least one class I study or 2 consistent class II studies. Level C recommendation indicates that the treatment is possibly effective, based on at least one class II study and 2 consistent class III studies.2

The grade of recommendation relates to the strength of the evidence on which the recommendation is based. It does not reflect the clinical importance of the recommendation.2

TD symptoms that have an impact on the patient should be managed with a VMAT2 inhibitor1,2

DISCOVER EFFICACY RESULTS FOR AUSTEDO

VMAT2, vesicular monoamine transporter 2.

REFERENCES: 1. Keepers GA, Fochtmann J, Anzia JM, et al. The American Psychiatric Association Practice Guideline for the Treatment of Patients With Schizophrenia. Third edition. Washington, DC: American Psychiatric Association; 2020. 2. Bhidayasiri R, Jitkritsadakul O, Friedman JH, Fahn S. Updating the recommendations for treatment of tardive syndromes: a systematic review of new evidence and practical treatment algorithm. J Neurol Sci. 2018;389:67-75.