Treatment non-persistence in children and adolescents with Tourette syndrome newly treated with dopamine D2 receptor modulators - Report - MDSpire

Treatment non-persistence in children and adolescents with Tourette syndrome newly treated with dopamine D2 receptor modulators

  • By

  • Kinga K. Tomczak

  • Jason P. Swindle

  • Firas M. Dabbous

  • Donald L. Gilbert

  • George B. Karkanias

  • Sarah D. Atkinson

  • Frederick E. Munschauer

  • Faizan Mazhar

  • Charlotte A. Pettersson

  • Stephen P. Wanaski

  • Timothy M. Cunniff

  • David A. Isaacs

  • June 2, 2026

  • 0 min

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Adherence Challenges in Pediatric Patients with Tourette Syndrome Initiated on Dopamine D2 Receptor Modulators

Overview

This study highlights the increased incidence of adverse events and healthcare resource utilization in pediatric patients with Tourette syndrome treated with dopamine D2 receptor modulators. Notably, there was a significant decline in documented medication records over time, indicating potential adherence challenges.

Background

Tourette syndrome (TS) is a prevalent neurodevelopmental disorder affecting children and adolescents, often leading to significant impairments in quality of life. The use of dopamine D2 receptor antagonists/partial agonists (D2RAs) for TS treatment is common, yet these medications are associated with serious adverse effects that may impact treatment adherence. Understanding the real-world implications of D2RA treatment is crucial for optimizing care in this population.

Data Highlights

CohortAdverse Events Odds Ratio (95% CI)Healthcare Resource Utilization Incidence Rate Ratio
D2RA-exposedMild: 3.36 (2.68–4.20), Moderate: 2.30 (1.65–3.20), Severe: 3.01 (2.18–4.16)1.39–4.10
D2RA-nonexposedReferenceReference

Key Findings

  • The D2RA-exposed cohort showed a decline in documented medication records from 38.8% at Month 3 to 17.9% at Month 18.
  • Higher odds of mild adverse events (e.g., sleep disorder) were observed in the D2RA-exposed cohort.
  • Moderate adverse events (e.g., QT prolongation) had an odds ratio of 2.30 in the D2RA-exposed cohort.
  • Severe adverse events (e.g., tardive dyskinesia) had an odds ratio of 3.01 in the D2RA-exposed cohort.
  • Increased healthcare resource utilization was noted in the D2RA-exposed cohort compared to the nonexposed cohort.
  • Findings suggest potential residual confounding by indication and greater disease severity in the treated cohort.

Clinical Implications

Clinicians should be aware of the high incidence of adverse events associated with D2RAs in pediatric TS patients, which may affect treatment adherence. Continuous monitoring and patient education are essential to manage these risks and optimize treatment outcomes.

Conclusion

The study underscores the need for careful consideration of the risks associated with D2RA treatment in pediatric patients with Tourette syndrome, highlighting the importance of adherence strategies and ongoing patient support.

Related Resources & Content

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  2. BMC Psychiatry, 2025 -- Objective evaluation of attention-deficit/hyperactivity disorder medication effects using a load-cell-embedded chair in a simulated classroom
  3. Drugs - Real World Outcomes, 2015 -- Temporal Analysis of Adverse Event Reporting for Dopamine Agonists in Australia
  4. Drug Safety, 2017 -- The Relationship Between Dopamine Agonists and Impulse Control Disorders: An Intricate Connection
  5. Practice guideline recommendations summary: Treatment of tics in people with Tourette syndrome and chronic tic disorders | Neurology, 2026
  6. Comparative efficacy, tolerability, and acceptability of pharmacological interventions for the treatment of children, adolescents, and young adults with Tourette's syndrome: a systematic review and network meta-analysis - ScienceDirect, 2022
  7. AAN Practice Guidelines on Tourette Syndrome Treatment
  8. Comparative efficacy, tolerability, and acceptability of pharmacological interventions for the treatment of children, adolescents, and young adults with Tourette's syndrome: a systematic review and network meta-analysis - ScienceDirect
  9. HIGHLIGHTS OF PRESCRIBING INFORMATION

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