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The Effectiveness of Pharmacological Treatments in Individuals with Autism

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Title: The Effectiveness of Pharmacological Treatments in Individuals with Autism


1
The Effectiveness of Pharmacological Treatments
in Individuals with Autism
  • November 13, 2003
  • Presentation by Chantal Bourgon

2
Outline
  • History, Prevalence and Demographic Variables
  • Neurochemistry, Effectiveness and Side
    Effects
    Antidepressants
  • Antipsychotics
  • Stimulants
  • Opiate Antagonists
  • Benzodiazepines
  • Alpha-2-Noradrenergic Agonists
  • Beta-Blockers
  • Take Home Message

3
History, Prevalence and Demographic Variables
  • Not until the late 1950s through 1970s did
    diverse pharmacological interventions emerge for
    individuals with autism.
  • The first symptoms targeted for drug treatment
    were destructive behaviours, self-injurious
    behaviours and aggression.
  • Autism Society of Ohio Study (2003)
  • 21.6 Antidepressants
  • 14.9 Antipsychotics
  • 12.5 Antihypertensives
  • 11.3 Stimulants

4
Cont
  • 25.7 One drug
  • 22.9 Two drugs
  • 6.4 Three or Four drugs
  • Demographic variables associated with medication
    use
  • Greater age
  • Severe Autism
  • Severe intellectual handicap
  • Housing outside the family home

5
Antidepressants
  • Tricyclic antidepressants
  • Venlafaxine
  • Target serotonergic neurotransmission
  • Increase concentration of serotonin in the
    synaptic space
  • Improved attention, social relatedness and
    communication
  • Decrease in hyperactivity
  • Improvement in restricted interest
  • Side effects possible hypertension (high blood
    pressure)

6
Cont
  • Tricylcic antidepressant Non-selective
    serotonin re-uptake
  • Clomipramine
  • Prevents serotonin re-uptake
  • Additional action on the dopaminergic system
  • Reduction in aggression persisting for 1.7 yrs
  • Improved social relatedness and
    obsessive-compulsive behaviours
  • Side effects possibility for grand mal seizure
    and cardiac conduction abnormality
  • Neurotoxic symptoms lead to its discontinuation

7
Cont
  • Selective Serotonin Re-uptake Inhibitor
  • Fluoxetine
  • Prevents serotonin re-uptake
  • Improvement in language, cognition, mood,
    compulsive symptoms, lethargy and stereotyped
    behaviours
  • Possible agitation, decrease in appetite,
    restlessness, anorexia, insomnia and increase in
    anxiety
  • Children are less responsive
  • Fluvoxamine
  • Prevents serotonin re-uptake
  • Improvement in repetitive thoughts and
    behaviours, aggression, social relatedness and
    language
  • Possibility for nausea and mild sedation

8
Antipsychotics
  • Typical
  • Haloperidol
  • Block a number of postsynaptic dopamine (DA)
    receptors (D2)
  • Superior to placebo in reducing stereotyped
    behaviours, withdrawal, hyperactivity, deviant
    speech and fidgetiness.
  • Side effects anxiety, depression, weight gain,
    parkinsonism, cognitive blunting and fatigue
  • Sedation dose dependent
  • Tardive dyskinesia disappear after
    discontinuation of medication
  • Prepubertal children are less responsive then
    adolescents and adults.

9
Cont
  • Atypical
  • Risperidone
  • Block DA receptors (D2) and block serotonin
    receptors
  • Positive response in terms of aggression, sleep,
    self-injurious behaviours, withdrawal, mood and
    social skills.
  • Improvement in disruptive behaviours for 2 yrs
    without any signs of tolerance
  • Improve tardive dyskinesia
  • Side effects weight gain but stabilizes with
    time
  • Sedation dose dependent
  • More useful in children suffering from severe and
    chronic autism

10
Stimulants
  • Pemoline
  • Increase DA and Norepinephrine (NE) in the
    synaptic cleft
  • Some studies show increase in agitation and
    repetitive behaviours
  • Other studies demonstrate some effectiveness
  • Side effects insomnia, weight loss, deceleration
    of growth, activation of tics in predisposed
    individuals, lower seizure threshold
  • Hepatoxicity and liver failure
  • Methyl phenidate
  • Affect dopaminergic neurotransmission
  • Decrease hyperactivity
  • Need more research

11
Opiate Antagonists
  • Naltrexone
  • Block the activity of endogenous opiate system in
    the central nervous system (C.N.S)
  • Minimum reduction in hyperactivity
  • No impairment in learning
  • No amelioration in social , stereotyped and
    self-injurious behaviours
  • No improvement in communication
  • Side effects mild and transient sedation and
    gastrointestinal upset
  • Bitter taste

12
Benzodiazepines
  • Lorazepam and Clonazepam
  • Act in concert with inhibitory neurotransmitter
    GABA to stabilize and decrease the firing rate of
    neurons.
  • Treat explosiveness and aggression which
    accompanies mental retardation.
  • Not systematically studied for autism
  • Side effects sedation, decrease reaction time,
    tolerance and dependence

13
Alpha-2-Noradrenergic Agonist
  • Clonidine
  • Decrease NE and Epinephrine neurotransmission
  • Pre-synaptic receptor agonist
  • Improvement in hyperactivity, inattention,
    impulsivity, irritability, stereotyped behaviours
    and inappropriate speech.
  • Side effects sedation, decrease in blood
    pressure and tolerance to therapeutic effects
  • Guanfacine
  • Decrease in activity, increase in arousal
  • Side effects hypotension

14
Beta-Blockers
  • Propanolol
  • Affects the noradrenergic transmission
  • Decrease impulsive and aggressive behaviours
  • Decrease in stereotyped and self-injurious
    behaviours
  • Improvement in attention span
  • Mitigate tremors induced by other drugs (Lithium)
  • Side effects, sedation, depression, drop in blood
    pressure and bradycardia (abnormally slow heart
    rate)

15
Others
  • Leuprolide
  • Antiandrogen
  • Inhibitor of gonadotropin secretion
  • Suppression of public masturbation
  • Decreased libido
  • No sexual excitement due to contact with children
  • Anticonvulsants
  • Lithium
  • Megavitamins
  • Corticosteroids
  • Secretin

16
Take Home Message
  • A number of classes of medication have been used
    to treat autism.
  • Pharmacological treatments are primarily
    symptomatic and benefits usually fade away as the
    medications are discontinued.
  • Need to increase understanding of developmental
    and neurochemical basis of autism to provide cues
    for novel use of medication.
  • Medication should always be part of a
    comprehensive multidisciplinary treatment
    approach.

17
References
  • Aman, M.G., Lam, K.S.L., Collier-Crespin, A.
    (2003) Prevalence and patterns of
  • use of psychoactive medicines among individuals
    with autism in the Autism Society of Ohio.
    Journal of Autism and Developmental Disorders,
    33, 527-534.
  • Buitelaar, J.K., Willemsen-Swinkels, S.H.N.
    (2000) Medication treatment in subjects with
    autism disorders. European Child and Adolescent
    Psychiatry, 9, 185- 197.
  • Fatemi, S.H., Realmuto, G.M., Khan, L., Thuras,
    P. (1998) Fluoxetine in treatment of adolescent
    patients with autism a longitudinal open trial.
    Journal of Autism and Developmental Disorders,
    28, 303-307.
  • Hellings, J.A. (1999) Psychopharmacology of mood
    disorders in persons with mental retardation and
    autism. Mental Retardation and Developmental
    Disabilities Research Reviews, 5, 270-278.
  • Hunsinger, D.M., Nguyen, T., Zebraski, S.E.,
    Raffa, R.B. (2000) Is there a basis for novel
    pharmacotherapy of autism? Life Sciences, 67,
    1667-1682.
  • Kerbeshian, J., Burd, L., Avery, K. (2001)
    Pharmacotherapy of autism A review and clinical
    approach. Journal of Developmental and Physical
    Disabilities, 13, 199-228.

18
Cont
  • Luiselli, J.K., Blew, P., Keane, J., Thibadeau,
    S., Holzman, T. (2000) Pharmacotherapy for
    severe aggression in a child with autism open
    label evaluation of multiple medications on
    response frequency and intensity of behavioural
    intervention. Journal of Behaviour Therapy and
    Experimental Psychiatry, 31, 219-230.
  • Realmuto, G.M., Ruble, L.A. (1999) Sexual
    behaviours in autism Problems of definition and
    management. Journal of Autism and Developmental
    Disorders, 29, 121-127.
  • Simeon, J., Milin, R., Walker, S. (2002) A
    retrospective chart review of Risperidone use in
    treatment-resistant children and adolescents with
    psychiatric disorders. Progress in
    Neuro-Psychopharmacology and Biological
    Psychiatry, 26, 267-275.
  • Williams, P.G., Allard, A., Sears, L., Dalrymple,
    N., Bloom, A.S. (2001) Brief report Case
    reports on Naltrexone use in children with
    autism Controlled observations regarding
    benefits and practical issues of medication
    management. Journal of Autism and Developmental
    Disorders, 31, 103-108.
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