Pharmacotherapy for hyperactivity in children with autism and other pervasive developmental disorders.
Old but useful map: antipsychotics, stimulants, and naltrexone lead for autism hyperactivity, yet later work shows we still need longer safety data.
01Research in Context
What this study did
Dawson et al. (2000) read every drug paper they could find on hyperactivity in kids with autism. They looked at antipsychotics, stimulants, and naltrexone. The team then wrote a plain list of which pills had the best proof at that time.
What they found
Three drug groups came out on top: antipsychotics like haloperidol, stimulants like Ritalin, and the blocker naltrexone. All three cut hyperactivity in small autism samples. The authors warned that most studies were short and weak.
How this fits with other research
Parsons et al. (2013) later updated the same question with 24 newer RCTs. Their paper supersedes Dawson et al. (2000) by showing the field still lacks long-term safety data.
Heavey et al. (2000) ran a tight RCT on methylphenidate in the same year. Their results extend the review by proving the drug helps, but irritability and withdrawal are common.
Skrtic et al. (1982) and Fovel et al. (1989) gave the first placebo proof that haloperidol calms behavior. Dawson et al. (2000) later folded these early trials into the "strong evidence" claim for antipsychotics.
Why it matters
If parents ask about pills for hyperactivity, you now know three classes with the oldest track record. Start the conversation with realistic hopes: benefits are modest and side effects are real. Always pair meds with behavior plans and collect data before and after dose changes so you can show what actually changes at school and home.
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02At a glance
03Original abstract
We reviewed pharmacological treatments used in children with autism and PDD-NOS who present with hyperactive symptoms. Some 41 studies were identified from the following drug categories: antipsychotics (n = 13), serotonin reuptake inhibitors (n = 3), antianxiety drugs (n = 4), psychostimulants (n = 10), alpha adrenergic agonists (n = 2), opiate blockers (n = 7), and other drugs (n = 2). Empirical evidence for significant reductions in hyperactive symptoms was strongest for the antipsychotics, psychostimulants, and naltrexone. Most studies have focused on the reduction of overactivity, and more emphasis needs to be placed on distractibility and attentional variables. A theoretical model was proposed in which participants' attentional performance may be used to predict clinical response to psychostimulants. More carefully controlled and comprehensive studies of hyperactivity are badly needed in these children.
Journal of autism and developmental disorders, 2000 · doi:10.1023/a:1005559725475