Tardive Dyskinesia: Treatment Update.

Divya Arya, Tarannum Khan, Adam J Margolius, Hubert H Fernandez

Journal: Current neurology and neuroscience reports 2020;19(9):69

PMID: 31420757

Abstract

PURPOSE OF REVIEW

Tardive dyskinesia (TD) is caused by exposure to medications with dopamine antagonism, mainly antipsychotics. It often distresses individuals, physically and emotionally and affects their quality of life. We evaluated peer-reviewed recently published articles with a goal of providing a critically appraised update on the latest advancements in this field.

RECENT FINDINGS

In 2017, FDA approved VMAT2 inhibitors, deutetrabenazine and valbenazine. They have demonstrated efficacy in several class 1 studies. Also there have been update in the evidence-based guidelines for treatment for tardive dyskinesia. Various medication classes are being used for treatment of TD with VMAT2 inhibitors to be first FDA-approved medications. Their use should be tailored to the individual patient. Long-term studies will further guide us in how to optimize treatment, especially in the real-world setting. As clinicians, we need to take into consideration all aspects of symptomatology, etiology, potential side effects of the medications, to find the best possible "match" for our patients.

Address: Pauline Braathen Neuroscince Institute, Cleveland Clinic Florida, Weston, FL, USA.; Center for Neurological Restoration, Cleveland Clinic, 9500 Euclid Avenue, S-3, Cleveland, OH, 44198, USA.; Center for Neurological Restoration, Cleveland Clinic, 9500 Euclid Avenue, S-3, Cleveland, OH, 44198, USA. [email protected].

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