Tics and dyskinesias associated with stimulant treatment in attention-deficit hyperactivity disorder

P H Lipkin1, I J Goldstein, A R Adesman

  • 1Department of Pediatrics, Schneider Children's Hospital, Long Island Jewish Medical Center, Albert Einstein College of Medicine, New Hyde Park, NY.

Insights

Approximately 9% of children with attention-deficit hyperactivity disorder (ADHD) experienced tics or dyskinesias (T/D) when treated with stimulant medication. Most cases were temporary, with less than 1% developing chronic tics or Tourette's syndrome.

Area of Science:

  • Pediatrics
  • Neurodevelopmental Disorders
  • Pharmacology

Background:

  • Stimulant medications are commonly prescribed for attention-deficit hyperactivity disorder (ADHD).
  • Concerns exist regarding potential side effects, including tics or dyskinesias (T/D).
  • Understanding the incidence and risk factors for T/D in children with ADHD is crucial for safe and effective treatment.

Purpose of the Study:

  • To determine the incidence of tics or dyskinesias (T/D) in children with ADHD treated with stimulant medications.
  • To examine associated clinical factors, such as age, medication type, dosage, and tic history, related to the onset of T/D.

Main Methods:

  • A cross-sectional analysis was conducted using chart review of a clinic cohort.
  • One hundred twenty-two children with ADHD treated with stimulant medication were included in the study.
  • Data collected included medication details, T/D presence and onset, and personal/family tic history.

Main Results:

  • The incidence of T/D was 9.0% among children or 8.2% of medication trials.
  • One child (0.8%) developed Tourette's syndrome.
  • No significant relationship was found between age, medication, dosage, or tic history and the onset of T/D.

Conclusions:

  • Approximately 9% of children with ADHD treated with stimulants developed T/D, mostly transient.
  • Fewer than 1% developed chronic tics or Tourette's syndrome.
  • Personal or family tic history, medication choice, or dosage did not predict T/D onset.
Abstract

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