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The Use of VMAT2 Inhibitors for Tardive Dyskinesia
Orges Alabaku1,2, Mark Olfson3,4, T Scott Stroup3
1Rutgers University Center for Pharmacoepidemiology and Treatment Science, New Brunswick.
Tardive dyskinesia (TD) diagnosis and treatment with vesicular monoamine transporter 2 inhibitors (VMAT2-Is) increased from 2017 to 2022. However, TD remains underdiagnosed, indicating a need for better recognition and access to VMAT2-Is.
Area of Science:
- Neuroscience
- Psychiatry
- Pharmacology
Background:
- Tardive dyskinesia (TD) is a movement disorder often associated with antipsychotic use.
- Vesicular monoamine transporter 2 inhibitors (VMAT2-Is) are FDA-approved treatments for TD, but their utilization patterns are not well-documented.
Purpose of the Study:
- To characterize trends in TD diagnosis and VMAT2-I use among adults with mental health conditions treated with antipsychotics.
- To identify predictors of VMAT2-I use in this population.
Main Methods:
- Analysis of 2017-2022 MarketScan data for adults aged 18-65.
- Identification of TD and mental health diagnoses via ICD-10 codes.
- VMAT2-I use determined from prescription claims; logistic regression used to assess predictors.
Main Results:
- TD diagnosis increased from 0.45% to 0.57%, and VMAT2-I use rose from 0.05% to 0.22% between 2017 and 2022.
- Predictors of VMAT2-I use included first-generation antipsychotic use, schizophrenia, bipolar disorder, female sex, and older age.
- Among TD patients, schizophrenia, bipolar disorder, and older age predicted VMAT2-I use.
Conclusions:
- TD diagnosis and VMAT2-I treatment rates show an increasing trend but remain low.
- The findings underscore the need for improved TD recognition and enhanced access to VMAT2-Is for eligible patients.
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