Methamphetamine Saskatchewan Provincial Webinar 2017 This webinar - - PowerPoint PPT Presentation
Methamphetamine Saskatchewan Provincial Webinar 2017 This webinar - - PowerPoint PPT Presentation
Methamphetamine Saskatchewan Provincial Webinar 2017 This webinar is brought to you in partnership by the Regional Health Authorities and the Ministry of Health. Housekeeping Background Introduction 4 Objectives Describe the
This webinar is brought to you in partnership by the Regional Health Authorities and the Ministry of Health.
- Housekeeping
- Background
- Introduction
Objectives
- Describe the history of stimulant use, including
current patterns.
- Explain the pharmacology and impact of
methamphetamine on the human body, particularly its potential to cause addiction.
- Understand the typical pattern for
methamphetamine intoxication, withdrawal and induced mental illness.
- Consider the implications for treatment.
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Presenter Disclosure
- No relevant commercial disclosures.
- Community based Associate Professor,
College of Medicine, University of Saskatchewan.
- Consultant on Addiction Medicine to
the Saskatoon Health Region.
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A Brief History of Stimulant Use
A Pinch of Snuff Verheyden, 1806 - 1890
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History of Stimulants
- Cocaine: chewing of coca leaves prevalent
in the Andean regions of South America for more than 2000 years
- 1860 German Graduate student Albert
Niemann, isolated cocaine as the active ingredient of coca leaf
- Coca-Cola: introduced 1886 (containing
4.5mg of cocaine per 6 oz.)
- 1903 cocaine removed from Coca-Cola
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History of Stimulants
- Amphetamine: first synthesized in 1887
- Methamphetamine: first synthesized in
1919
- Amphetamines widely used during WWII
- Methamphetamine currently available
with a prescription for obesity, attention deficit hyperactivity disorder, and narcolepsy ex: Desoxyn
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History of Stimulants
- Ecstasy: used unsuccessfully in
psychotherapy in 1970’s, became popular in rave scene in late 1980’s, early 1990’s.
- Crack Cocaine: 1984/1985 appears in New
York, Los Angeles and Miami.
- In late 1980’s smokable form of Crystal Meth
was created in Asia and then surfaced in California in the 1990’s, spread west to east.
- Use waxes and wanes in different regions.
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Canadian Methamphetamine Use
- Canadian Addiction Survey (2004) – 15 & over:
– 6.4% used at least once in lifetime – Less than 1% reported use in last year
- Peak use during late adolescence/early
adulthood (15-30 years)
- Use more common in street involved youth, gay
men and homeless populations
– 71% of a convenience sample of street involved youth in Vancouver had used – 37% of homeless youth in Toronto used at least once a month.
CCSA 2006
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Canadian Methamphetamine Use Summary
- West >> East
- Predominately (but not exclusively) marginalized
populations, “Out of Care’s Way”
- 1 in 10 who use become dependent
- Few dependent users present for treatment
CCSA 2006
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Stimulant Use in Saskatchewan
- Unique predilection for IV methylphenidate.
- Decreased with introduction of tamper
resistant Concerta, but coincided with increase in cocaine use.
- Methamphetamine transiently significant in
late 1990’s - early 2000’s.
- More significant in last 4 years.
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Crystal Methamphetamine Chemistry and Action
Photo: USA DEA
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Crystal Meth
- Chemically similar to amphetamines
- White, odourless, bitter-tasting
crystalline powder
- Route: oral, smoked, snorted, or
injected
- Made in illegal labs by chemically
altering OTC medicines (pseudoephedrine)
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Pharmacology of Stimulants
- Water soluble
- Onset of action depends on route of
administration: rapid onset of action with injection or smoking
- Duration of action dependent on route of
administration and chemistry: oral administration produces longer duration of action, methamphetamine persists longer than amphetamine.
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Central Nervous System Effect
- Methamphetamine
– Inhibit reuptake of synaptic dopamine AND promotes direct dopamine release – Promotes catecholamine (adrenalin, noradrenalin) release. *Direct effect on dopamine creates the greatest likelihood of dependency.
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Progression to Addiction
- Loss of normal reward and motivational
systems.
- Everything becomes drug focused.
- It becomes harder to feel “high”.
- One then uses simply to feel “normal” and
avoid depression or withdrawal.
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From Getting High to Being Down
- High
- Normal
- Down
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Metabolism and Excretion
- Metabolizes from methamphetamine to
amphetamine.
- Excreted in urine.
- UDS may show: methamphetamine,
methamphetamine and amphetamine, or amphetamine.
- Prescription amphetamines also test positive
as amphetamines on UDS.
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Prescription Amphetamines
- Dextroamphetamine Sulphate
(Dexedrine)
- Amphetamine and
Dextroamphetamine (Adderall)
- Lisdexamfetamine (Vyvanse)
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Clinical Effects of Methamphetamine
Intoxication Withdrawal Stimulant Induced Mental Illness
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Stimulant Intoxication
- Signs or Symptoms
- 1. Tachycardia or bradycardia
- 2. Pupillary dilation
- 3. Elevated or lowered blood pressure
- 4. Perspiration or chills
- 5. Nausea or vomiting
- 6. Evidence of weight loss
- 7. Psychomotor agitation or retardation
- 8. Muscular weakness, respiratory depression, chest
pain, or cardiac arrhythmias
- 9. Confusion, seizures, dyskinesias, dystonias, or coma
DSM 5 23
Stimulant Intoxication
- Problematic behavioural or psychological
changes:
- 1. euphoria or affective blunting
- 2. changes in sociability
- 3. hypervigilance
- 4. interpersonal sensitivity
- 5. anxiety
- 6. tension or anger
- 7. stereotyped behaviours
- 8. impaired judgement
DSM 5 24
Stimulant Intoxication Treatment
- ART = Acceptance, Reassurance, Talk down
(if not psychotic)
- Quiet, soft lit room.
- Benzodiazepines preferred over antipsychotics
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Acute Consequences of Stimulant Use
- Neuro: seizures, strokes
- CVS: tachycardia, arrythmia, MI,
HTN
- Kidneys: cocaine induced
rhabdomyolysis
- Blood: Agranulocytosis (levamisole)
- Obstetrics: placenta previa
- ENT: nosebleeds
- Infectious Disease: STI’s, cellulitis,
bacterial endocarditis, HIV, HCV.
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Stimulant Withdrawal
- Dysphoric mood and two (or more) of the
following, developing within hours to several days after cessation of prolonged stimulant use
- 1. Fatigue
- 2. Vivid, unpleasant dreams
- 3. Insomnia or hypersomnia
- 4. Increased appetite
- 5. Psychomotor retardation, or agitation
DSM 5 27
Stimulant Withdrawal
- Rarely require hospitalization or medications
- Supportive treatment
- Impulsivity and craving problematic
- Managed, efficient transition to treatment
- Residential treatment superior to outpatient
treatment
- Relapse prevention skills need to be
instituted early
- Suicide prevention
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Stimulant Induced Mental Health Disorders
INTOXICATION WITHDRAWAL Psychotic Delusions Bipolar Bipolar Depression Depression Anxiety Anxiety OCD OCD Sleep Disorders Sleep Disorders Sexual Dysfunction DSM 5 29
Stimulant Induced Psychosis
- Agitation, irritability, paranoia, hallucinations
(tactile), thought form disorder, delirium.
- Schizophrenia: more auditory hallucinations,
clear sensorium, persistent symptoms, negative symptoms, bizarre delusions.
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Treatment of Psychosis
- Similar environment as with intoxication.
- Olanzapine 10 mg IM or 15 mg po
- Risperidone 2 mg. OD - BID
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Long Term Consequences of Stimulant Use
- Tolerance and Withdrawal
- Sensitization
- Addiction (Stimulant Use Disorder)
- Restlessness, anxiety, irritability,
paranoia, panic attacks, mood disturbances
- Insomnia
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Sensitization
- Sensitization (opposite of tolerance)
more you use the drugs more likely of symptoms happening such as:
– Seizure – Psychosis (paranoia, visual, auditory, and tactile hallucinations) – Stereotypical behaviors
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Long Term Consequences
- Reproduction: irregular menses, prematurity
- ENT: nasal septum perforation, loss of sense
- f smell, chronically runny nose
- Infectious Disease: HCV, HIV
- Weight loss
- Neurocognitive impairment
- Dental: “meth mouth”
- Psychosocial: homelessness, legal
involvement, trauma
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Methamphetamine and HIV/AIDS
- Increased use of transmission through IVDU,
contaminated pipes and unprotected sex.
- Ongoing use and treatment avoidance
interferes with 1) engagement and 2) retention in care.
- Inability to take meds daily results in
progression of HIV to AIDS and death.
- May be hastened by increased
catecholamine, cortisol and immune suppression.
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Methamphetamine and HIV/AIDS
- Progression to AIDS and death most
commonly associated with ongoing stimulant use. (WSCC data)
- People on OAT for Opioid Use Disorder may
relapse on methamphetamine. Retention in care often compromised by lack of attendance at pharmacy or clinic, and sub-
- ptimal use of ART for HIV.
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Effects of Crystal Meth
36 Permission granted by Multnomah County Sheriff’s Office
TREATMENT Transitioning from chaos into care.
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The Complexity of Active Addiction
- Typically psychosocial chaos. May be street
and / or gang involved. May be homeless. Disrupted education or vocation. Often legal consequences from crime or sex trade work to obtain drugs.
- Personal growth and development typically
disrupted.
- Often poly-substance use: drugs and
alcohol.
- Highly marginalized and stigmatized.
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The Complexity of Active Addiction
- Frequently associated with concurrent health issues
- Mental health, either pre-existing or drug induced:
mood, anxiety disorders or psychosis.
- Blood borne infections: HIV, AIDS, HCV.
- Other infections: superficial abscesses, heart, lung,
bone, joints, nervous system (spine and brain) and / or deep pelvic abscesses.
- Poor nutrition.
- Sub-optimal care.
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Personal Context
- Security: food, shelter, safety, income
- Addiction: diagnosis, consequences, stage,
stability
- Readiness: stage of change, denial vs. gains
- Co-morbidity: medical and psychological
- Competency: coping skills, education,
training
- Often hard to reach, or “Out of Help’s Way”.
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Treatment of Stimulant Use Disorders
- SBIRT (Screening, Brief Intervention, Referral to
Treatment)
- Harm Reduction (needle exchange/crack pipe
programs)
- Motivational Enhancement Therapy
- Cognitive Behavioural Therapy
- Contingency Management
- Residential Treatment
- Self Help Support
- Treatment of Underlying Mental Health Disorders
- Treat any Medical Complications (HIV, HCV)
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CBT for Stimulant Use Disorders
- Identification of high risk
situations
- Development of coping skills
- Development of new lifestyle
behaviours
- Development of sense of self-
efficacy
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Risk of Relapse
- Drug exposure
- Cues: users, high risk sites, paraphernalia
- Mood: stress, depression
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Emergency and Detox Implications
- Quiet, secure longer term detox.
- Appropriate but assertive use of anti-
psychotics.
- Focused psychiatric consults for persistent
psychosis or concurrent disorder care.
- Increased concurrent psychiatric care
capacity.
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Treatment Implications
- Drug court intervention.
- Longer term residential treatment,
therapeutic housing, supportive residences
- r Mental Health Group Home models.
- Mobilization of CBO and private sectors in
conjoined housing and treatment partnerships.
- Linkage to housing support, education,
vocational training or return to work.
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Treatment Works!
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References
- DSM 5 Diagnostic & Statistical Manual of
Mental Disorders 5th Ed. Text Revision 2013
- The ASAM Principles of Addiction
Medicine Fifth Edition. Ries, Fiellin, Miller,
- Saitz. 2014
- The Canadian Tobacco, Alcohol and
Drugs Survey (CTADS) 2013
- National Institute of Drug Abuse (NIDA)
www.drugabuse.gov
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Thank You! Questions?
Contact: peter.butt@usask.ca
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