medication and behavioral treatment of substance use disorders · 2018-11-19 · casacolumbia....
TRANSCRIPT
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Medication and Behavioral Treatment
of Substance Use Disorders
Brian Fuehrlein, MD, PhD
Director, Psychiatric Emergency Room, VA
Connecticut and Assistant Professor of
Psychiatry, Yale University
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Brian Fuehrlein, Disclosures
I have no financial relationships to disclose.
The contents of this activity may include discussion of off label or investigative drug uses. The faculty is aware that is their responsibility to disclose this information.
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Planning Committee, Disclosures
AAAP aims to provide educational information that is balanced, independent, objective and free of bias
and based on evidence. In order to resolve any identified Conflicts of Interest, disclosure information from
all planners, faculty and anyone in the position to control content is provided during the planning process
to ensure resolution of any identified conflicts. This disclosure information is listed below:
The following developers and planning committee members have reported that they have no
commercial relationships relevant to the content of this module to disclose: PCSS-MAT lead
contributors Frances Levin, MD and Adam Bisaga, MD; AAAP CME/CPD Committee Members Dean
Krahn, MD, Kevin Sevarino, MD, PhD, Tim Fong, MD, Tom Kosten, MD, Joji Suzuki, MD; and AAAP
Staff Kathryn Cates-Wessel, Miriam Giles, Carol Johnson and Justina Pereira.
All faculty have been advised that any recommendations involving clinical medicine must be based on
evidence that is accepted within the profession of medicine as adequate justification for their indications
and contraindications in the care of patients. All scientific research referred to, reported, or used in the
presentation must conform to the generally accepted standards of experimental design, data collection,
and analysis. The content of this CME activity has been reviewed and the committee determined the
presentation is balanced, independent, and free of any commercial bias. Speakers will inform the learners
if their presentation will include discussion of unlabeled/investigational use of commercial products.
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Target Audience
The overarching goal of PCSS-MAT is to make
available the most effective medication-assisted
treatments to serve patients in a variety of settings,
including primary care, psychiatric care, and pain
management settings.
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Educational Objectives
At the conclusion of this activity participants should be able to:
Identify the primary medications in the treatment of
alcohol use disorder
Define the primary medications in the treatment of opioid
use disorder
Describe the primary options for psychosocial treatment
and support
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Substance use disorder is a chronic relapsing and
remitting illness
A multimodal approach of medications and
psychosocial treatment and support is considered
the most effective for opioid and alcohol use
disorder
Withdrawal management is not treatment
Review
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Case Presentation #1
Bob is a 50-year-old male with chronic alcohol use disorder.
Recently completed court-ordered detox then
30-day residential treatment
Relapsed upon discharge from treatment
due to cravings
Ambivalent about sobriety
Lives alone
Diagnosed with cirrhosis and coronary artery disease
Has been prescribed low dose opioids for chronic back pain
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• Steve is a 27-year-old man diagnosed
with alcohol use disorder
• Recently completed a 90-day treatment
program and remains sober, but struggles
with cravings 2-3 times per week
• Generally prefers not taking medications but is willing to try
• Committed to recovery, attends daily AA meetings
• No medical problems
• Lives with a supportive family
Case Presentation #2
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Denise is a 40-year-old woman with alcohol use
use disorder
Recently arrested for 3rd DUI
Currently in court-ordered intensive outpatient
program
Denies cravings
Highly motivated by legal pressures
Inquired about a medication that will prevent her
from drinking
Lives with husband who is willing to do whatever
it takes to help her
No medical problems
Case Presentation #3
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Alcohol Use Disorder
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Disulfiram (Antabuse)
Approved in 1957 for alcohol use disorder
Aversive therapy, does not reduce cravings
Inhibits aldehyde dehydrogenase
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Increasing levels of acetaldehyde causes an
aversive reaction
Leads to tachycardia, flushing, nausea,
vomiting, hypotension
Within hours of first dose and days to weeks
after last dose
Must fully educate patients about these risks
Most effective with motivated patients
Most effective with supervised administration
Disulfiram (Antabuse)
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Starting and maintenance dose 250-500mg daily
Metabolized through liver and LFTs should be checked and monitored
Patients should be alcohol free for >12 hours
Occasional aversive reactions from hidden alcohol sources are possible
Must educate patient about the possibility of a severe reaction with
alcohol consumption
Severe myocardial disease, coronary occlusion and severe liver
disease are contraindications while psychosis is a relative
contraindication
Disulfiram (Antabuse)
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Naltrexone
Orally available mu opioid
receptor antagonist, not to be
confused with naloxone
Alcohol causes endogenous
opioid release and reinforcing
effects
Naltrexone reduces cravings and the positive reinforcing effects of
alcohol
Naltrexone reduces amount consumed when drinking
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Naltrexone
Orally once daily starting and maintenance dose is 25-50mg
Patients must be opioid free for >7 days for standard opioids and 10-14 days for long acting opioids like methadone
Obtain baseline liver function tests including AST, ALT, and total bilirubin prior to instituting naltrexone (oral or injectable) therapy. Only initiate therapy if liver function tests (LFTS) are lower than 5x the upper limit of normal (ULN).
Obtain follow-up AST and ALT levels approximately 8-12 weeks after initiation of naltrexone with quarterly monitoring thereafter
Side effects are generally mild and include nausea, headache, dizziness, fatigue and insomnia
Hepatotoxicity is a black box warning though is rare
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Extended Release Naltrexone (VivitrolTM)
• Once-a-month and injectable into gluteal muscle
Injection site reactions are a possible side effect
Consider a trial of oral naltrexone
Avoids first-pass metabolism hence total dose is lower (380mg)
Patients should not be prescribed opioids and this should be confirmed with a
urine drug screen or naloxone challenge
Patients had longer time of sobriety and fewer drinking days per month
Particularly effective following at least 4 days of abstinence, though may also be
used in those actively drinking
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Acamprosate (CampralTM)
NMDA receptor modulator and GABA/glutamate
stabilization
May also stabilize the hypothalamic pituitary axis
These actions offer neuroprotection and reduce the
post-acute withdrawal symptoms of anxiety and
irritability, which may contribute to a relapse
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Acamprosate (CampralTM)
Reduces the risk of return to drinking
Increases the duration of abstinence
Likely as effective as naltrexone
Well tolerated and not metabolized through the liver
Gastro-intestinal side effects are most common
Therapeutic dose is 666mg TID (6 pills per day)
Adherence is the primary problem
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Topiramate (TopamaxR)
Off-label use for alcohol use disorder to reduce post-acute withdrawal symptoms and craving
Facilitates GABA and antagonized glutamate and may decrease dopamine activity in the reward pathway and reduce withdrawal symptoms
Has shown efficacy in doses 75-300 mg daily and is better tolerated if titrated slowly
Compared to placebo, reduced drinks per day, number of heavy drinking days and days of abstinence
Primary side effect is cognitive slowing
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Gabapentin (NeurontinR)
• Indicated for seizure disorder, restless leg syndrome and
postherpetic pain
• Off-label use for alcohol use disorder (among other things)
GABA receptor agonist
Very mild side effect profile and very well tolerated
Dosed up to 1200 mg TID
Results are promising
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Medication Assisted Treatment
for Opioid Use Disorder
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Methadone
What does methadone have to do with this?
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Methadone
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Methadone Pharmacology
Full mu opioid receptor agonist
Half life 24 - 36 hours
Increased risk of respiratory depression and
overdose when mixed with alcohol and/or
benzodiazepines
Very effective at doses >80 - 140mg once daily
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CASAColumbia. (2012). Addiction medicine: Closing the gap between science and practice.
Methadone Mechanism of Action
Being a full agonist with a long half-life, methadone
suppresses signs and symptoms of opioid withdrawal by
reaching a steady-state level with once daily dosing
It eliminates opioid cravings
May also serve to block the reinforcing effects of illicit
opioids
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Methadone Delivery
For treatment of OUD, methadone must
be administered in a federally regulated
opioid treatment program
Patients are seen daily for administered
dosing with gradually increasing take home
privileges on symptom improvement
Once per week visits is the least restrictive
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Methadone Side Effects
Respiratory depression, particularly with benzos or alcohol
Prolonged QTc at doses >100mg, if seen daily
Weight gain
Constipation
Decreased testosterone
Dry mouth
Urinary retention
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Buprenorphine
DATA 2000 permitted scheduled III-V
medications to treat opioid use disorder in an
office-based setting
Buprenorphine is schedule III
Synthetic opioid that functions as a partial agonist at the mu opioid receptor
Partial agonist effect serves to reduce cravings and eliminate withdrawal
Unlike full agonists, partial agonists create a ceiling effect at higher doses – thus no increased respiratory depression or euphoria at higher doses
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Buprenorphine Pharmacology
Compared to methadone, buprenorphine has a reduced overdose potential and improved
safety profile
Partial agonist may precipitate withdrawal if taken by someone who is taking daily doses of a
full agonist – need to be in mild withdrawal before taking first dose
Buprenorphine has a high affinity to the mu receptor and results in blocking other opioids
This may result in precipitated withdrawal
• This blocks other full agonist misuse
Formulated with naloxone (4:1 ratio) to reduce misuse and diversion – naloxone is not
bioavailable unless injected
Available in tablets, films, and long-acting implant
Buprenorphine is as effective as methadone except for treatment retention
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Extended-Release Naltrexone
Opioid antagonist
Provides complete blockade of the mu opioid receptors (though may be
overridden in emergency situations for acute pain control)
Counterintuitively, may actually reduce cravings for opioids (different
mechanism than methadone/buprenorphine)
Studies are underway to determine efficacy compared to buprenorphine
and methadone
Daily oral naltrexone is generally not recommended for OUD given
problems with medication adherence
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Pharmacotherapy for Opioid Use Disorder
no drug high dose
Drug Dose
low dose
%
Mu Receptor
Intrinsic
Activity
0
10
20
30
40
50
60
70
80
90
100
Full Agonist: Methadone Full Agonist: Methadone
Partial Agonist: Buprenorphine
Antagonist: Naltrexone
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Behavioral Treatment and
Psychosocial Supports for SUDs
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Evidence-Based Therapy
Evidence-based therapy should be used in conjunction with medications when possible.
For substances without an approved medication, evidence-based therapy can be one of the primary means of sobriety.
Evidence-based therapies include CBT1, CRAFT2 and CM3
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Cognitive Behavioral Therapy
• In maladaptive behavioral patterns, learning
plays a critical role
• Teach patients to identify and correct problematic
behaviors by applying learned skills
• Anticipating problems and enhancing self control
by developing coping strategies
• Exploring consequences, self monitoring for
cravings early and identifying risky situations
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CRAFT
Community Reinforcement and Family Training
Increase family compliance with an
intervention to increase the rate of treatment
for the patient
• Motivation building, functional analysis,
communication skill training, life enrichment
and other skills
• Targets the family of those with substance
use disorders
• Has been shown to improve engagement in
treatment
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Contingency Management
Highly effective in increasing treatment retention and promoting abstinence
Provides tangible rewards to reinforce positive behaviors, such as abstinence
Voucher based reinforcement involves vouchers that are exchanged for goods and services
Vouchers increase in value with more negative urine drug screens
Prize incentives provide chances to win cash prizes
Each negative urine is a chance to win
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Psychosocial Recovery Supports
Psychosocial recovery supports, while not evidence-
based therapies, are potentially very important and very
helpful.
When medications and other evidence-based therapies
are not available, psychosocial supports may be all that
is available
The primary psychosocial supports include Alcoholics
Anonymous, SMART Recovery and supportive
psychotherapy
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Alcoholics Anonymous
Founded in 1935
“Primary purpose is to stay sober and help other alcoholics achieve sobriety”
“The only requirement for AA membership is a desire to stop
drinking”
No cost, no side effects, readily available and may greatly benefit the patient
Nearly all patients with a substance use disorder will be familiar with AA, their providers should be too
AA is the primary psychosocial support available
Tonigan, S., et al. Participation and involvement
in Alcoholics Anonymous, 2003
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Alcoholics Anonymous
The recovery program
• Meetings (90 in 90)
• Sponsorship
• Step work
• Commitments
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Alcoholics Anonymous
Meetings
• 90 meetings in 90 days is the minimum
recommended starting point
• Meetings are widely available, often
have themes and many attend daily
meetings indefinitely
Sponsorship
• “A sponsor is one person to turn to without embarrassment
when doubts, questions or problems linked to alcoholism
arise”
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Alcoholics Anonymous
Step work
• Step 1: We admitted we were
powerless over alcohol and our lives
had become unmanageable
• There are twelve steps that should be
worked through as part of the recovery
program
Commitments
• Commitment can be small, i.e., will make coffee at a particular meeting, or large, i.e., becoming a sponsor
• This shows responsibility to something or someone other than self
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SMART Recovery
Self Management And Recovery Training
Alternative or supplement to AA
Non confrontational motivational, behavioral and cognitive methods
Meetings are integral to the program
SMART recovery relies less on religion and
spirituality
Four point program
• Building motivation
• Coping with urges
• Problem solving
• Lifestyle balance Horvath, T. and Yeterian, J. “SMART Recovery: Self-Empowering, Science-Based
Addiction Recovery Support. Journal of Groups in Addiction Recovery, 7:102-117, 2012
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Supportive Recovery Psychotherapy
The primary goal is to strengthen the ability to cope with stressors
Close, empathetic listening
Reinforcing and strengthening resilience
Building and maintaining self-esteem
Encourage sharing of feelings and thoughts
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Summary
Medications are an integral part of substance use
disorder treatment
Only a handful of medications are currently
approved, with others under investigation
Psychosocial supports may be used in conjunction
with medications and may be particularly important
when medications or behavioral treatments are not
available
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References
Fuehrlein and Gold. Medication assisted recovery in alcohol and
opioid dependence. Directions in Psychiatry. 33(2):15-29, 2013
Horvath, T. and Yeterian, J. “SMART Recovery: Self-Empowering,
Science-Based Addiction Recovery Support. Journal of Groups in
Addiction Recovery, 7:102-117, 2012
Meyers, R. and Smith, J. Clinical Guide to Alcohol Treatment: The
Community Reinforcement Approach. Guildford Press, 1995
Newman, C. Cognitive Therapy of Substance Abuse. The
Guildford Press, 1993
Tonigan, S., et al. Participation and involvement in Alcoholics
Anonymous, 2003
Prendergast, M., et al. Contingency management for treatment of
substance use disorders: a meta-analysis. Addiction,
101(11):1546-1560, 2006
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PCSS-MAT Mentoring Program
PCSS-MAT Mentor Program is designed to offer general information to
clinicians about evidence-based clinical practices in prescribing
medications for opioid addiction.
PCSS-MAT Mentors are a national network of providers with expertise in
addictions, pain, evidence-based treatment including medication-
assisted treatment.
• 3-tiered approach allows every mentor/mentee relationship to be unique
and catered to the specific needs of the mentee.
• No cost.
For more information visit:
pcssmat.org/mentoring
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Funding for this initiative was made possible (in part) by grant no. 1U79TI026556-01 from SAMHSA. The views expressed in written
conference materials or publications and by speakers and moderators do not necessarily reflect the official policies of the Department
of Health and Human Services; nor does mention of trade names, commercial practices, or organizations imply endorsement by the
U.S. Government.
PCSS-MAT is a collaborative effort led by the American Academy of Addiction Psychiatry (AAAP) in
partnership with the: Addiction Technology Transfer Center (ATTC); American Academy of Family
Physicians (AAFP); American Academy of Pain Medicine (AAPM); American Academy of Pediatrics
(AAP); American College of Emergency Physicians (ACEP); American College of Physicians (ACP);
American Dental Association (ADA); American Medical Association (AMA); American Osteopathic
Academy of Addiction Medicine (AOAAM); American Psychiatric Association (APA); American
Psychiatric Nurses Association (APNA); American Society of Addiction Medicine (ASAM); American
Society for Pain Management Nursing (ASPMN); Association for Medical Education and Research in
Substance Abuse (AMERSA); International Nurses Society on Addictions (IntNSA); National
Association of Community Health Centers (NACHC); and the National Association of Drug Court
Professionals (NADCP).
For more information: www.pcssmat.org
Twitter: @PCSSProjects
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PCSS-MAT: Training, Mentoring, Resources