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PRINCIPLES OF MANAGEMENT OF STIMULANT MISUSE

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Title: PRINCIPLES OF MANAGEMENT OF STIMULANT MISUSE


1
PRINCIPLES OF MANAGEMENT OF STIMULANT MISUSE
  • DR ALISON BATTERSBY

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Amphetamine
  • Class of synthetic drugs similar effect to
    adrenalin
  • Act by releasing noradrenalin and dopamine and
    inhibiting reuptake.
  • D and L forms (D twice as powerful as a central
    stimulant)

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Group of compounds
  • Amphetamine
  • Methamphetamine
  • Fenfluramine
  • Bupropion
  • Mephedrone

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  • Synthesised in Germany in 1887
  • Nasal decongestants until 1930s
  • Medically tested on hospital workers in 30s to
    create wellbeing and relieve fatigue
  • WW11 to combat fatigue
  • OTC in 50s, POM in 60s
  • Second most commonly injected drug

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Effects
  • Elevated mood
  • Feel more energetic, alert and self-confident
  • Improved task performance
  • Decreased fatigue and hunger
  • May be more talkative, restless or agitated
  • Increased libido

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  • Increased heart rate, BP
  • Palpitations
  • Dilated pupils
  • Dry mouth
  • Sweating
  • L-amphetamine greater cardiovascular effects

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Intoxication
  • Dizziness
  • Sweating
  • Chest pain
  • Palpitation
  • Hypertension
  • Cardiac arrhythmias
  • May increase body temp/convulsions

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Tolerance
  • To some but not all aspects
  • To gain euphoric effect may need to escalate dose
  • Cardiovascular effects
  • Appetite suppression
  • Used therapeutically for narcolepsy and
    hyperkinetic disorders

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Physical Dependence
  • Disputed
  • After a run abrupt withdrawal the crash
  • Fatigue, depression, hunger
  • Irritability
  • Anxiety/agitation
  • ?normal reaction

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Psychological dependence
  • Definitely present
  • Intense craving
  • drug-seeking behaviour
  • Powerful reinforcer in animal experiments

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Adverse effects
  • Psychotic illness
  • Often persecutory in nature
  • Automatic stereotyped behaviour
  • Irritability
  • Paranoia
  • Aggression

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Mode of Action Dopamine and Serotonin
  • Causes presynaptic dopamine vesicles to release
    dopamine into cytosol
  • Causes reversal of the DAT (dopamine active )
    transporters so it transports Dopamine into the
    cleft
  • Reversal of the SERT (serotonin) transporter
    particularly in mesocorticolimbic pathways
    increasing glutamatergic neurons

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Physical Sequelae
  • Cardiovascular, HT, Pulse, cardiomyopathy, aortic
    dissction
  • CNS ischaemic strokes, intracerebral
    haemorrhages, seizure, abnormal movements
  • Ischaemic colitis
  • Rhabdomyolysis
  • hepatotoxicity

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Methamphetamine
  • Common nicknames, ice, crystal meth, crank,
    glass, speed, shabu (philippines), tik (south
    africa) and ya ba (thailand)
  • Oral, snorting, smoking, injection

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Pharmacology
  • ½ life 9-15 hrs excreted by kidney
  • Lipid soluble, fast entry to brain
  • Resistance to MAO degradation
  • Causes reversal of dopamine, NA uptake enzymes
  • Tolerance occurs partially due to transmitter
    depletion
  • Neurotoxic to dopamine and serotonin neurons

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Effects
  • Desired euphoria, alertness, concentration, self
    confidence, energy
  • Unwanted aggression, agitation, irritability,
    paranoia, psychosis
  • Physical anorexia, tachycardia, hypertension,
    constipation, palpitations, stroke, MI,
    convulsions

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Production
  • Combination of red phosphorus, pseudoephedrine
    and iodine
  • Extremely dangerous

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Long term effects
  • Meth mouth, dry mouth, grinding teeth
  • Injecting related problems
  • Unsafe sex
  • Withdrawal excessive sleeping, increased
    appetite and depression, often accompanied by
    anxiety and drug craving

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Amphetamine psychosis
  • 309 regular amphetamine users
  • 13 screened positive for psychosis
  • 23 clinically significant symptoms of
    suspiciousness, unusual thought content or
    hallucinations in the past year
  • Swift onset
  • Delusions and hallucinations may mimic bipolar or
    schizophrenia
  • Abates within days with restoration of sleep and
    cessation of amphetamines

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Treatment of Amphetamine Dependence
  • Mainly semi-structured psychosocial interventions
  • Substitution therapies, evidence is equivocal or
    poor quality
  • Occasional use of modafinil, baclofen,
    mirtazapine and naltrexone
  • High dose venlafaxine/SSRIs when use stopped

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Cocaine
  • Alkaloid prepared from coca bush
  • Erythroxylum coca
  • Central and south america
  • Leaves chewed alleviate fatigue, hunger and cold
  • Incas religious ceremonies, social and medicinal

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  • First isolated 1880s
  • Oral consumption widespread
  • Used in tonics
  • Freud noted local anaesthetic and psychic effects
  • Recommended it for treatment opiate addiction

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Coca-cola (old-style)
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Manufacture
  • Illegal factories close to growth
  • Cocaine hydrochloride obtained
  • White powder
  • Easy to transport
  • Cut eg sugar, amphetamine, beta blockers

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Route of administration
  • Sniffing/snorting (line inhaled through straw)
  • Vasoconstriction of blood vessels
  • No rush, 20-40minute effect
  • Rhinitis/perforated nasal septum
  • Iv

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  • Smoking
  • Cocaine hydrochloride unsuitable for smoking
    (decomposes high temps)
  • Alkaloid can be freed from hydrochloride by using
    ether, vaporises easily

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Crack
  • Cooking cocaine with baking powder and water
  • Baking powder precipitates impurities
  • Pure crystalline cocaine
  • Usually smoked in pipe or sprinkled on cigarette
  • Sudden intense high

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  • Reaches brain within seconds
  • Euphoria abates quickly
  • User feels restless and irritable
  • Marked craving
  • Use often escalates quickly to chase the high

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Effects
  • CNS stimulant
  • Increased energy, wakefulness, activity and
    confidence
  • Powerful euphoriant eg Brompton cocktail
  • Raised pulse, blood pressure, temperature
  • Dilated pupils
  • Local vasoconstriction

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Very high doses
  • Hypertension
  • Cardiac arrythmias
  • Convulsions
  • Death (cardiac/respiratory arrest)

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Tolerance
  • Some degree of tolerance with pure cocaine
    freebase
  • Ceiling tolerance level
  • No tolerance to reinforcing effect

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Physical dependence
  • Withdrawal
  • Crash thirty minutes after a binge
  • Social withdrawal, depression, tremor, muscle
    pain, disturbance of sleeping, eating
  • Dysphoria, intense craving
  • Extinction phase 3-12 months

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Psychological dependence
  • Severe
  • Animal model, powerful reinforcer
  • Mechanism of action not fully understood
  • Specific cocaine receptors
  • Affects dopaminergic system, inhibit dopamine
    reuptake

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Long-term use
  • Excessive dopamine metabolised
  • Therefore reduced dopamine concentration
  • Then changes in post-synaptic receptors (craving)
  • Also acts on NA and 5HT systems inhibiting
    reuptake

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Cocaine toxicity/psychosis
  • Anxiety, restlessness, apprehension,
    suspiciousness, hypervigilence, paranoid
    behaviour
  • Muscle twitching, nausea, vomiting
  • Increase pulse and blood pressure
  • Irregular respiration
  • convulsions

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Severe toxicity
  • Circulatory failure
  • Respiratory failure
  • Loss of reflexes
  • Unconsciousness
  • death

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Cocaine psychosis
  • Persecutory delusions
  • Stereotyped behviour
  • Auditory hallucinations
  • Tactile hallucinations (cocaine bugs)

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Treatment
  • Not as well defined as for opiate addiction
  • Psychosocial interventions using semi-structured
    interviews
  • Acupuncture

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Ketamine
  • Developed 1962 by Pfizer
  • Used as a general anaesthetic or in pain relief
  • NMDA (Glutamate) receptor antagonist
  • Action particularly in the prefrontal cortex and
    hippocampus
  • At higher levels binds opioid receptors, partial
    D2 agonist and inhibits dopamine reuptake

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Illicit use
  • Sold in powder or liquid
  • Can be sniffed, injected or swallowed
  • Significant first pass metabolism so larger
    amounts needed if swallowed
  • Class C drug
  • Dependence rare, tolerance develops reasonably
    quickly, no abstinence syndrome?

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Effects
  • Dissociative amnesia k-hole
  • Feelings of detachment from the world
    depersonalisation/derealisation
  • Spiritual experiences
  • Feeling connected to others
  • Visual hallucinations, other perceptual
    abnormalities
  • Changes in time
  • Lasts about 2 hours

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Health consequences
  • Bladder problems- BMJ 2008 case series of 9
    patients dose-related
  • Severe urinary frequency, urgency, macroscopic
    haematuria, suprapubic pain
  • Changes in cognition, heavy users worse verbal
    short-term memory and visual memory
  • Occasional users no different from controls
  • Overdose, commonly from iv use

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Questions please
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