Volume 20 | September 2025

On the Front Line: Helping Advanced Practice Providers to Recognize, Assess, and Treat Tardive Dyskinesia

Clinical
Empowering Mental Health Advanced Practice Providers to Screen, Diagnose, and Appropriately Treat Tardive Dyskinesia
Empowering Mental Health Advanced Practice Providers to Screen, Diagnose, and Appropriately Treat Tardive Dyskinesia





Approximately 1 in 4 adults in the United States experiences a mental illness.1 At the same time, there has been a decrease in the number of psychiatrists, underscoring the importance of a robust workforce of healthcare professionals, including psychiatric-mental health advanced practice providers (APPs), composed of nurse practitioners (NPs) and physician assistants (PAs).2,3 This article provides mental health APPs with an overview of tardive dyskinesia (TD), a movement disorder resulting from exposure to antipsychotic drugs.4 It also explores the multifaceted impact of TD on patients’ lives.

The Growing Role of NPs and PAs in Mental Healthcare

In 2023, it was estimated that approximately 59 million US adults, or 23% of the adult population, experienced a mental illness, and nearly half of those individuals did not receive treatment.1 Mental healthcare clinicians can range from psychiatrists, psychologists, NPs, and PAs to social workers, and from solo practitioners to multidisciplinary teams.5-7

Compounding this crisis is a growing shortage of psychiatrists, with projections from the US Health Resources and Services Administration (HRSA) predicting a deficit of 18,000 to 21,000 professionals by 2030, suggesting that an expanding number of people of all ages will have unmet behavioral health needs.1,2 Due to this accelerating demand for mental healthcare professionals, NPs and PAs are an increasingly vital resource for managing patients with mental health disorders.3 According to the HRSA, 11,310 new NPs and PAs are expected to join the workforce by 2030, highlighting the essential role of these providers in meeting the rising demand for mental healthcare and mitigating the shortage of psychiatrists.8

NPs and PAs play a critical role in addressing the growing need for mental healthcare in the midst of the mental health crisis.
Overview and Clinical Presentation of TD

Dopamine receptor blocking agents such as atypical and typical antipsychotics are commonly used to treat a variety of psychiatric disorders. It is known that they may cause side effects, including movement disorders such as TD, drug-induced parkinsonism (DIP), akathisia, and dystonia.9

TD is a persistent, typically irreversible, hyperkinetic movement disorder that affects approximately 785,000 individuals in the US.4,10,11 Despite this prevalence, TD may be underdiagnosed and undertreated, with approximately 15% of patients receiving a formal diagnosis and less than 6% being treated with vesicular monoamine transporter 2 (VMAT2) inhibitors, the only FDA-approved treatments for TD.11-13 While TD primarily affects the face, it can also impact any part of the body, including the trunk and extremities (Video 1).14

Video 1. Clinical Presentations of TD

Patient images used with permission.

Impact of TD on Patients’ Lives

According to an online survey of patients, TD can hinder a clinician’s ability to manage a patient’s underlying mental health condition.15

  • 48% reported they skipped doses of an antipsychotic medication or took less than the doctor instructed
  • 39% reported they stopped taking antipsychotic medication altogether
  • 36% stopped going to the doctor for treatment of their underlying condition
  • 21% advised someone else not to take an antipsychotic medication

One of the challenges in assessing the impact of TD on patients is that the clinician’s perception of mild movements may not equal the patient’s experience of impact.16 The disconnect between movement severity, as observed by the clinician, and impact, as experienced by the patient, is illustrated in Videos 2 and 3 below.

Video 2. Patient’s Movements (No Sound)
The visual assessment of TD is mild
Video 3. Patient Impact From TD (With Sound)
The verbal description of TD indicates significant impact

Patient images used with permission.

Any presentation of TD can have a profound impact on various aspects of patients’ lives such as their capacity to carry out daily tasks, maintain productivity, and engage in social activities.17-19 TD manifestations such as these can complicate the management of the underlying mental health disorder.20

The clinician’s perception of mild TD movements may not equal the patient’s experience of impact.
Findings From the IMPACT-TD Registry Study

Historically, it was believed that the severity of TD movements dictated the overall impact on the patient. However, more recently it has become evident that movement severity is only part of the equation, and TD can have a broader impact on patients’ lives.21 To more fully comprehend the impact of TD, the IMPACT-TD Registry study was established to systematically collect data across various domains of patients’ lives. This study was the first of its kind, and its objective was to significantly enhance the understanding of TD.22

A key finding from this interim analysis was that patients with symptoms that were considered mild, based on measurements taken by a healthcare professional, can experience a moderate to severe impact of TD. Notably, this study revealed that 54% of patients with very mild or 61% with mild TD (based on the Clinical Global Impression of Severity of TD) experienced a moderate to severe impact on the clinician IMPACT-TD global score. Furthermore, approximately 74% of patients with an Abnormal Involuntary Movement Scale (AIMS) score of 1 to 6 reported moderate to severe impact from TD.16

Additionally, the impact of movements extended into the social, psychological, physical, and vocational/educational/recreational dimensions of patients’ lives, with 83% indicating moderate to severe impact in at least 1 domain.16 Patients have reported that TD had an impact on the following23

  • ~60% said their movements prevented them from leaving the house
  • >75% reported feeling embarrassed in social situations
  • >60% said movements impacted their sleep
  • >50% reported their movements limited them at work

Presented below are testimonials from patients conveying the impact of TD in their own words across various domains studied in the IMPACT-TD Registry study (Videos 4-7).

Video 4. Social Domain
Video 5. Psychological/Psychiatric Domain
Video 6. Physical Domain
Video 5. Psychological/Psychiatric Domain

Patient images used with permission.

The IMPACT-TD Registry study revealed that more than half of patients with mild TD symptoms experienced a moderate to severe impact, affecting the social, psychological, physical, and vocational/educational/recreational aspects of their lives.
Assessing the Impact of TD in Clinical Practice

Managing patients treated with antipsychotics involves not only screening for and assessing TD movements but also understanding the wider impact TD has on patients, their families, and caregivers.24-26 There may also be a discrepancy between the severity of movements observed by the clinician and the impact as experienced by the patient.16 Thus, it is essential to look for any abnormal movements and ask questions to gauge the impact of these movements at every clinical encounter (Figure).18,24,27,28

Figure. In all patients with current or previous exposure to antipsychotics4,18, 25,29
Figures

Per American Psychiatric Association (APA) Guidelines, VMAT2 inhibitors are recommended if TD has an impact on the patient, regardless of the severity of movements.25

Managing patients on antipsychotics requires not only screening for and evaluating TD movements but also comprehending the impact on patients and their social circle.
Summary
  • Amid the mental health crisis and psychiatrist shortage in the US, the demand for mental healthcare professionals is growing1-3
  • Psychiatric mental health NPs and PAs have a critical role in filling this gap3
  • In recent years, the number of antipsychotic prescriptions has increased, resulting in an increased prevalence of TD, a hyperkinetic and often irreversible movement disorder4,10,11
  • Data from the groundbreaking IMPACT-TD Registry study shows that TD movements, regardless of severity, can impact patients across the social, psychological, physical, and vocational/educational/recreational aspects of their lives16
  • Assessment of TD impact should be performed at every clinical visit24
  • The APA Guidelines support treatment of TD that has an impact on the patient with VMAT2 inhibitors, regardless of severity of movements25
References
1. HRSA Health Workforce. State of the behavioral health workforce, 2024. Accessed March 17, 2025. https://bhw.hrsa.gov/sites/default/files/bureau-health-workforce/state-of-the-behavioral-health-workforce-report-2024.pdf 2. HRSA Health Workforce. Behavioral health workforce projections, 2016-2030: psychiatrists (adult), child and adolescent psychiatrists. Accessed March 17, 2025. https://bhw.hrsa.gov/sites/default/files/bureau-health-workforce/data-research/psychiatrists-2018.pdf 3. Cai A, Mehrotra A, Germack HD, Busch AB, Huskamp HA, Barnett ML. Trends in mental health care delivery by psychiatrists and nurse practitioners in Medicare, 2011-19. Health Aff (Millwood). 2022;41(9):1222-1230. 4. Hauser RA, Meyer JM, Factor SA, et al. Differentiating tardive dyskinesia: a video-based review of antipsychotic-induced movement disorders in clinical practice. CNS Spectr. 2022;27(2):208-217. 5. Haines A, Perkins E, Evans EA, McCabe R. Multidisciplinary team functioning and decision making within forensic mental health. Ment Health Rev (Brighton). 2018;23(3):185-196. 6. Delaney KR. Inclusion of psychiatric-mental health advanced practice nurses in federal behavioral workforce planning. Psychiatr Serv. 2024;75(6):594-596. 7. Bruza-Augatis M, Kozikowski A, Hooker RS, Puckett K. Physician assistants/associates in psychiatry: a workforce analysis. Hum Resour Health. 2024;22(1):40. 8. HRSA Health Workforce. Behavioral health workforce projections, 2016-2030: psychiatric nurse practitioners, psychiatric physician assistants. Accessed March 17, 2025. https://bhw.hrsa.gov/sites/default/files/bureau-health-workforce/data-research/physician-assistants-2018.pdf 9. Duma SR, Fung VS. Drug-induced movement disorders. Aust Prescr. 2019;42(2):56-61. 10. The tardive syndromes: phenomenology, concepts on pathophysiology and treatment, and other neuroleptic-induced syndromes. In: Fahn S, Jankovic J, Hallett M, eds. Principles and Practice of Movement Disorders. 2nd ed. Elsevier, Inc; 2011:415-446. 11. Data on file. Teva Neuroscience, Inc. Parsippany, NJ. 12. AUSTEDO XR® (deutetrabenazine) extended-release tablets/AUSTEDO® current Prescribing Information. Parsippany, NJ: Teva Neuroscience, Inc. 13. Ingrezza® (valbenazine) capsules. Prescribing Information. San Diego, CA: Neurocrine Biosciences, Inc. 14. Takeuchi H, Mori Y, Tsutsumi Y. Pathophysiology, prognosis and treatment of tardive dyskinesia. Ther Adv Psychopharmacol. 2022;12:20451253221117313. 15. Jain R, Ayyagari R, Goldschmidt D, et al. Impact of tardive dyskinesia on physical, psychological, social, and professional domains of patient lives: a survey of patients in the United States. J Clin Psychiatry. 2023;84(3):22m14694. 16. Finkbeiner S, Konings M, Henegar M, et al. Multidimensional impact of tardive dyskinesia: interim analysis of clinician-reported measures in the IMPACT-TD Registry. Presented at: Psych Congress Elevate; May 30-June 2, 2024; Las Vegas, NV. 17. Caroff SN, Yeomans K, Lenderking WR, et al. RE-KINECT: a prospective study of the presence and healthcare burden of tardive dyskinesia in clinical practice settings. J Clin Psychopharmacol. 2020;40(3):259-268. 18. Jackson R, Brams MN, Citrome L, et al. Assessment of the impact of tardive dyskinesia in clinical practice: consensus panel recommendations. Neuropsychiatr Dis Treat. 2021;17:1589-1597. 19. Ascher-Svanum H, Zhu B, Faries D, et al. Tardive dyskinesia and the 3-year course of schizophrenia: results from a large, prospective, naturalistic study. J Clin Psychiatry. 2008;69(10):1580-1588. 20. Caroff SN, Davis VG, Miller DD, et al. Treatment outcomes of patients with tardive dyskinesia and chronic schizophrenia. J Clin Psychiatry. 2011;72(3):295-303. 21. Strassnig M, Rosenfeld A, Harvey PD. Tardive dyskinesia: motor system impairments, cognition and everyday functioning. CNS Spectr. 2018;23(6):370-377. 22. Teva Neuroscience, Inc. Teva presents first real-world data from the IMPACT-TD Registry study at Psych Congress Elevate 2024. Accessed March 17, 2025. https://www.tevapharm.com/news-and-media/latest-news/teva-presents-first-real-world-data-from-the-impact-td-registry-study-at-psych-congress-elevate-2024/23. Finkbeiner S, Konings M, Henegar M, et al. Interim analysis of a patient-reported impact measure in the IMPACT-TD Registry. Presented at: Annual Psych Congress Elevate; May 30-June 2, 2024; Las Vegas, NV. 24. Caroff SN, Citrome L, Meyer J, et al. A modified Delphi consensus study of the screening, diagnosis, and treatment of tardive dyskinesia. J Clin Psychiatry. 2020;81(2):19cs12983. 25. American Psychiatric Association. The American Psychiatric Association Practice Guideline for the Treatment of Patients With Schizophrenia. 3rd ed. Washington, DC: American Psychiatric Association; 2021. Accessed March 17, 2025. https://psychiatryonline.org/doi/pdf/10.1176/appi.books.9780890424841 26. Jain R, Ayyagari R, Goldschmidt D, Zhou M, Finkbeiner S, Leo S. Impact of tardive dyskinesia on patients and caregivers: a survey of caregivers in the United States. J Patient Rep Outcomes. 2023;7(1):122. 27. Gulko C. Tardive dyskinesia: tips on conducting patient-focused exams. Accessed March 17, 2025. https://www.medpagetoday.com/resource-centers/tardive-dyskinesia-contemporary-approaches/tardive-dyskinesia-tips-conducting-patient-focused-exams/3347 28. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. 5th ed, Text Revision. American Psychiatric Association; 2022. 29. Ward KM, Citrome L. Antipsychotic-related movement disorders: drug-induced parkinsonism vs. tardive dyskinesia—key differences in pathophysiology and clinical management. Neurol Ther. 2018;7(2):233-248.
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Uncovering, Identifying, and Addressing Tardive Dyskinesia: Strategies for Assessment and Treatment
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IMPORTANT SAFETY INFORMATION
Depression and Suicidality in Patients with Huntington's Disease: AUSTEDO XR and AUSTEDO can increase the risk of depression and suicidal thoughts and behavior (suicidality) in patients with Huntington's disease. Balance the risks of depression and suicidality with the clinical need for treatment of chorea. Closely monitor patients for the emergence or worsening of depression, suicidality, or unusual changes in behavior. Inform patients, their caregivers, and families of the risk of
IMPORTANT SAFETY INFORMATION
Depression and Suicidality in Patients with Huntington's Disease: AUSTEDO XR and AUSTEDO can increase the risk of depression
INDICATIONS AND USAGE

AUSTEDO XR® (deutetrabenazine) extended-release tablets and AUSTEDO® (deutetrabenazine) tablets are indicated in adults for the treatment of chorea associated with Huntington's disease and for the treatment of tardive dyskinesia.

IMPORTANT SAFETY INFORMATION
Depression and Suicidality in Patients with Huntington's Disease: AUSTEDO XR and AUSTEDO can increase the risk of depression and suicidal thoughts and behavior (suicidality) in patients with Huntington's disease. Balance the risks of depression and suicidality with the clinical need for treatment of chorea. Closely monitor patients for the emergence or worsening of depression, suicidality, or unusual changes in behavior. Inform patients, their caregivers, and families of the risk of depression and suicidality and instruct them to report behaviors of concern promptly to the treating physician. Exercise caution when treating patients with a history of depression or prior suicide attempts or ideation. AUSTEDO XR and AUSTEDO are contraindicated in patients who are suicidal, and in patients with untreated or inadequately treated depression.
Contraindications AUSTEDO XR and AUSTEDO are contraindicated in patients with Huntington's disease who are suicidal, or have untreated or inadequately treated depression. AUSTEDO XR and AUSTEDO are also contraindicated in: patients with hepatic impairment; patients taking reserpine or within 20 days of discontinuing reserpine; patients taking monoamine oxidase inhibitors (MAOIs), or within 14 days of discontinuing MAOI therapy; and patients taking tetrabenazine or valbenazine.
Clinical Worsening and Adverse Events in Patients with Huntington's Disease: AUSTEDO XR and AUSTEDO may cause a worsening in mood, cognition, rigidity, and functional capacity. Prescribers should periodically re-evaluate the need for AUSTEDO XR or AUSTEDO in their patients by assessing the effect on chorea and possible adverse effects.
QTc Prolongation: AUSTEDO XR and AUSTEDO may prolong the QT interval, but the degree of QT prolongation is not clinically significant when AUSTEDO XR or AUSTEDO is administered within the recommended dosage range. AUSTEDO XR and AUSTEDO should be avoided in patients with congenital long QT syndrome and in patients with a history of cardiac arrhythmias.
Neuroleptic Malignant Syndrome (NMS), a potentially fatal symptom complex reported in association with drugs that reduce dopaminergic transmission, has been observed in patients receiving tetrabenazine. The risk may be increased by concomitant use of dopamine antagonists or antipsychotics. The management of NMS should include immediate discontinuation of AUSTEDO XR and AUSTEDO; intensive symptomatic treatment and medical monitoring; and treatment of any concomitant serious medical problems.
Akathisia, Agitation, and Restlessness: AUSTEDO XR and AUSTEDO may increase the risk of akathisia, agitation, and restlessness. The risk of akathisia may be increased by concomitant use of dopamine antagonists or antipsychotics. If a patient develops akathisia, the AUSTEDO XR or AUSTEDO dose should be reduced; some patients may require discontinuation of therapy.
Parkinsonism: AUSTEDO XR and AUSTEDO may cause parkinsonism in patients with Huntington's disease or tardive dyskinesia. Parkinsonism has also been observed with other VMAT2 inhibitors. The risk of parkinsonism may be increased by concomitant use of dopamine antagonists or antipsychotics. If a patient develops parkinsonism, the AUSTEDO XR or AUSTEDO dose should be reduced; some patients may require discontinuation of therapy.
Sedation and Somnolence: Sedation is a common dose-limiting adverse reaction of AUSTEDO XR and AUSTEDO. Patients should not perform activities requiring mental alertness, such as operating a motor vehicle or hazardous machinery, until they are on a maintenance dose of AUSTEDO XR or AUSTEDO and know how the drug affects them. Concomitant use of alcohol or other sedating drugs may have additive effects and worsen sedation and somnolence.
Hyperprolactinemia: Tetrabenazine elevates serum prolactin concentrations in humans. If there is a clinical suspicion of symptomatic hyperprolactinemia, appropriate laboratory testing should be done and consideration should be given to discontinuation of AUSTEDO XR and AUSTEDO.
Binding to Melanin-Containing Tissues: Deutetrabenazine or its metabolites bind to melanin-containing tissues and could accumulate in these tissues over time. Prescribers should be aware of the possibility of long-term ophthalmologic effects.
Common Adverse Reactions: The most common adverse reactions for AUSTEDO (>8% and greater than placebo) in a controlled clinical study in patients with Huntington's disease were somnolence, diarrhea, dry mouth, and fatigue. The most common adverse reactions for AUSTEDO (4% and greater than placebo) in controlled clinical studies in patients with tardive dyskinesia were nasopharyngitis and insomnia. Adverse reactions with AUSTEDO XR extended-release tablets are expected to be similar to AUSTEDO tablets.
Please see accompanying full Prescribing Information, including Boxed Warning.
INDICATIONS AND USAGE

AUSTEDO XR® (deutetrabenazine) extended-release tablets and AUSTEDO® (deutetrabenazine) tablets are indicated in adults for the treatment of chorea associated with Huntington's disease and for the treatment of tardive dyskinesia.

IMPORTANT SAFETY INFORMATION
Depression and Suicidality in Patients with Huntington's Disease: AUSTEDO XR and AUSTEDO can increase the risk of depression and suicidal thoughts and behavior (suicidality) in patients with Huntington's disease. Balance the risks of depression and suicidality with the clinical need for treatment of chorea. Closely monitor patients for the emergence or worsening of depression, suicidality, or unusual changes in behavior. Inform patients, their caregivers, and families of the risk of depression and suicidality and instruct them to report behaviors of concern promptly to the treating physician. Exercise caution when treating patients with a history of depression or prior suicide attempts or ideation. AUSTEDO XR and AUSTEDO are contraindicated in patients who are suicidal, and in patients with untreated or inadequately treated depression.
Contraindications AUSTEDO XR and AUSTEDO are contraindicated in patients with Huntington's disease who are suicidal, or have untreated or inadequately treated depression. AUSTEDO XR and AUSTEDO are also contraindicated in: patients with hepatic impairment; patients taking reserpine or within 20 days of discontinuing reserpine; patients taking monoamine oxidase inhibitors (MAOIs), or within 14 days of discontinuing MAOI therapy; and patients taking tetrabenazine or valbenazine.
Clinical Worsening and Adverse Events in Patients with Huntington's Disease: AUSTEDO XR and AUSTEDO may cause a worsening in mood, cognition, rigidity, and functional capacity. Prescribers should periodically re-evaluate the need for AUSTEDO XR or AUSTEDO in their patients by assessing the effect on chorea and possible adverse effects.
QTc Prolongation: AUSTEDO XR and AUSTEDO may prolong the QT interval, but the degree of QT prolongation is not clinically significant when AUSTEDO XR or AUSTEDO is administered within the recommended dosage range. AUSTEDO XR and AUSTEDO should be avoided in patients with congenital long QT syndrome and in patients with a history of cardiac arrhythmias.
Neuroleptic Malignant Syndrome (NMS), a potentially fatal symptom complex reported in association with drugs that reduce dopaminergic transmission, has been observed in patients receiving tetrabenazine. The risk may be increased by concomitant use of dopamine antagonists or antipsychotics. The management of NMS should include immediate discontinuation of AUSTEDO XR and AUSTEDO; intensive symptomatic treatment and medical monitoring; and treatment of any concomitant serious medical problems.
Akathisia, Agitation, and Restlessness: AUSTEDO XR and AUSTEDO may increase the risk of akathisia, agitation, and restlessness. The risk of akathisia may be increased by concomitant use of dopamine antagonists or antipsychotics. If a patient develops akathisia, the AUSTEDO XR or AUSTEDO dose should be reduced; some patients may require discontinuation of therapy.
Parkinsonism: AUSTEDO XR and AUSTEDO may cause parkinsonism in patients with Huntington's disease or tardive dyskinesia. Parkinsonism has also been observed with other VMAT2 inhibitors. The risk of parkinsonism may be increased by concomitant use of dopamine antagonists or antipsychotics. If a patient develops parkinsonism, the AUSTEDO XR or AUSTEDO dose should be reduced; some patients may require discontinuation of therapy.
Sedation and Somnolence: Sedation is a common dose-limiting adverse reaction of AUSTEDO XR and AUSTEDO. Patients should not perform activities requiring mental alertness, such as operating a motor vehicle or hazardous machinery, until they are on a maintenance dose of AUSTEDO XR or AUSTEDO and know how the drug affects them. Concomitant use of alcohol or other sedating drugs may have additive effects and worsen sedation and somnolence.
Hyperprolactinemia: Tetrabenazine elevates serum prolactin concentrations in humans. If there is a clinical suspicion of symptomatic hyperprolactinemia, appropriate laboratory testing should be done and consideration should be given to discontinuation of AUSTEDO XR and AUSTEDO.
Binding to Melanin-Containing Tissues: Deutetrabenazine or its metabolites bind to melanin-containing tissues and could accumulate in these tissues over time. Prescribers should be aware of the possibility of long-term ophthalmologic effects.
Common Adverse Reactions: The most common adverse reactions for AUSTEDO (>8% and greater than placebo) in a controlled clinical study in patients with Huntington's disease were somnolence, diarrhea, dry mouth, and fatigue. The most common adverse reactions for AUSTEDO (4% and greater than placebo) in controlled clinical studies in patients with tardive dyskinesia were nasopharyngitis and insomnia. Adverse reactions with AUSTEDO XR extended-release tablets are expected to be similar to AUSTEDO tablets.
Please see accompanying full Prescribing Information, including Boxed Warning.