Methamphetamine Saskatchewan Provincial Webinar 2017 This webinar - - PowerPoint PPT Presentation

methamphetamine saskatchewan provincial webinar 2017
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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


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Methamphetamine Saskatchewan Provincial Webinar 2017

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This webinar is brought to you in partnership by the Regional Health Authorities and the Ministry of Health.

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  • Housekeeping
  • Background
  • Introduction
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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

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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

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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

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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

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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

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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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