Medication-Assisted Treatment (MAT) of Opiad Dependence Christina M. Delos Reyes, MD Jan 2012

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List three different types of MAT (medication-assisted treatment) for opioid dependence …

List three different types of MAT (medication-assisted treatment) for opioid dependence

Describe the mechanism of action and the proper dosing for three different types of MAT for opioid dependence

Review common barriers to using MAT in a variety of treatment settings.

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  • 1. Medication-Assisted Treatment (MAT) of Opioid Dependence Christina M. Delos Reyes, MD Chief Clinical Officer, ADAMHS Board of Cuyahoga CountyMedical Consultant, Center for Evidence-Based Practices at Case SAMHSA/BJA Opiate Treatment Grant Training Cleveland, Ohio January 26 & 27, 2012 1
  • 2. Learning Objectives Following this presentation, participants will be able to: • List three different types of MAT (medication- assisted treatment) for opioid dependence • Describe the mechanism of action and the proper dosing for three different types of MAT for opioid dependence. • Review common barriers to using MAT in a variety of treatment settings. 2
  • 3. Ritual of a Heroin User “A Fort Myers woman in her 30s prepares a heroin fix at the home of a friend on a recent day. The woman uses a hypodermic needle to inject heroin, which she had heated in a spoonful of water, into a vein in her hand. However, the increased purity of the drug and a fear of contracting HIV from contaminated needles, along with the social stigma associated with needle use, has caused an upsurge in users snorting and smoking heroin. "You first get an adrenaline rush, then a sensation of mellow. You lose sense of time and forget everything, the woman said. "Heroin is easy to find...You can get a bag for $10.” 3SOURCE: Naples Daily News, 2001.
  • 4. Opiate/Opioid : What’s the Difference? Opiate A term that refers to drugs or medications that are derived from the opium poppy, such as heroin, morphine, and codeine. Opioid A more general term that includes opiates as well as the synthetic drugs or medications, such as buprenorphine, methadone, meperidine (Demerol®), fentanyl—that produce analgesia and other effects similar to morphine. 4
  • 5. Basic Opioid FactsDescription: Opium-derived, or synthetics which relieve pain, produce morphine-like addiction, and relieve withdrawal from opioidsMedical Uses: Pain relief, cough suppression, diarrheaMethods of Use: Intravenously injected, smoked, snorted, or orally administered 5
  • 6. What’s What? Agonists, Partial Agonists, and AntagonistsAgonist Morphine-like effect (e.g., heroin)Partial Agonist Maximum effect is less than a full agonist (e.g., buprenorphine)Antagonist No effect in absence of an opiate or opiate dependence (e.g., naloxone) 6
  • 7. Opioid Agonists Natural derivatives of opium poppy - Opium - Morphine - Codeine 7
  • 8. Opium 8SOURCE: www.streetdrugs.org
  • 9. Morphine 9SOURCE: www.streetdrugs.org
  • 10. Opioid Agonists Semisynthetics: Derived from chemicals in opium - Diacetylmorphine – Heroin - Hydromorphone – Dilaudid® - Oxycodone – Percodan®, Percocet® - Hydrocodone – Vicodin® 10
  • 11. Heroin 11SOURCE: www.streetdrugs.org
  • 12. 12
  • 13. Opioid Agonists 13SOURCE: www.pdrhealth.com
  • 14. Opioid Agonists Synthetics - Propoxyphene – Darvon®, Darvocet® - Meperidine – Demerol® - Fentanyl citrate – Fentanyl® - Methadone – Dolophine® - Levo-alpha-acetylmethadol – ORLAAM® 14
  • 15. Methado ne Darvocet 15SOURCE: www.methadoneaddiction.net
  • 16. Opioid Partial Agonists Buprenorphine – Buprenex®, Suboxone®, Subutex® Pentazocine – Talwin® 16
  • 17. Buprenorphine/Naloxone combination and Buprenorphine Alone 17
  • 18. Opioid Antagonists Naloxone – Narcan® Naltrexone – ReVia®, Trexan® 18
  • 19. Opioids and the Brain: Pharmacology and Half-Life 19
  • 20. 20SOURCE: National Institute on Drug Abuse, www.nida.nih.gov.
  • 21. TerminologyReceptor: specific cell binding site or molecule: a molecule, group, or site that is in a cell or on a cell surface and binds with a specific molecule, antigen, hormone, or antibody 21
  • 22. Opioid Agonists: Pharmacology Stimulate opioid receptors in central nervous system & gastrointestinal tract Analgesia – pain relief (somatic & psychological) Antitussive action – cough suppression Euphoria, stuperousness, “nodding” Respiratory depression 22
  • 23. Opioid Agonists: Pharmacology Pupillary constriction (miosis) Constipation Histamine release (itching, bronchial constriction) Reduced gonadotropin secretion Tolerance, cross-tolerance Withdrawal: acute & protracted 23
  • 24. What is the Definition of “Half-Life?” The time it takes for half a given amount of asubstance such as a drug to be removed from living tissue through natural biological activity 24
  • 25. Duration of Action Two factors determine the duration of action of the medication:• Half-life - time it takes to metabolize half the drug. In general, the longer the half-life, the longer the duration of action.• Receptor affinity or strength of the bond between the substance and the receptor - medications that bind strongly to the receptor may have very long action even though the half-life may be quite short. 25
  • 26. Opioid Antagonist Half- Lives Naloxone – 15-30 minutes Naltrexone – 24-72 hours 26
  • 27. Opioid Agonist Half-Lives Heroin, codeine, morphine – 2-4 hours Methadone – 24 hours LAAM – 48-72 hours 27
  • 28. Opioid Partial Agonist Half-Lives Buprenorphine – 4-6 hours (however, duration of action very long due to high receptor affinity) Pentazocine – 2-4 hours 28
  • 29. Opioid Addictionand the Brain Opioids attach to receptors in brain Pleasure Repeated opioid use Tolerance Absence of opioids after prolonged use Withdrawal 29
  • 30. What Happens When You Use Opioids? Acute Effects: Sedation, euphoria, pupil constriction, constipation, itching, and lowered pulse, respiration and blood pressure Results of Chronic Use: Tolerance, addiction, medical complications Withdrawal Symptoms: Sweating, gooseflesh, yawning, chills, runny nose, tearing, nausea, vomiting, diarrhea, and muscle and joint aches 30
  • 31. Possible Acute Effects of Opioid Use Surge of pleasurable sensation = “rush” Warm flushing of skin Dry mouth Heavy feeling in extremities Drowsiness Clouding of mental function Slowing of heart rate and breathing Nausea, vomiting, and severe itching 31
  • 32. Consequences of Opioid Use  Addiction  Overdose  Death  Use related (e.g., HIV infection, malnutrition)  Negative consequences from injection: • Infectious diseases (e.g., HIV/AIDS, Hepatitis B and C) • Collapsed veins • Bacterial infections • Abscesses • Infection of heart lining and valves • Arthritis and other rheumatologic problems 32
  • 33. Heroin Withdrawal Syndrome  Intensity varies with level & chronicity of use  Cessation of opioids causes a rebound in function altered by chronic use  First signs occur shortly before next scheduled dose  Duration of withdrawal is dependent upon the half- life of the drug used: • Peak of withdrawal occurs 36 to 72 hours after last dose • Acute symptoms subside over 3 to 7 days • Protracted symptoms may linger for weeks or months 33
  • 34. Opioid Withdrawal Syndrome Acute Symptoms Pupillary dilation Lacrimation (watery eyes) Rhinorrhea (runny nose) Muscle spasms (“kicking”) Yawning, sweating, chills, gooseflesh Stomach cramps, diarrhea, vomiting Restlessness, anxiety, irritability 34
  • 35. Opioid Withdrawal Syndrome Protracted Symptoms Deep muscle aches and pains Insomnia, disturbed sleep Poor appetite Reduced libido, impotence, anorgasmia Depressed mood, anhedonia Drug craving and obsession 35
  • 36. Treatment Options for Opioid-Addicted Individuals Behavioral treatments educate patients about the conditioning process and teach relapse prevention strategies. Medications such as methadone and buprenorphine operate on the opioid receptors to relieve craving. Combining the two types of treatment enables patients to stop using opioids and return to more stable and productive lives. 36
  • 37. Treatment Options for Opioid-Addicted Individuals Medically-assisted withdrawal Long-term residential treatment Outpatient psychosocial treatment Behavioral therapies Medication-Assisted Treatment (MAT) 37
  • 38. Medication-Assisted Treatment Naltrexone—antagonist Methadone—agonist Buprenorphine—partial agonist 38
  • 39. Naltrexone Opiate antagonist to treat opiate dependence All effects of opiates are blocked • Must be detoxed and opiate-free or else will cause opiate withdrawal syndrome Blocks opioid receptors that are involved in the rewarding effects of opiates (& alcohol!) Risk for hepatotoxicity • Monitor for liver enzymes 39
  • 40. Naltrexone Brand name: Revia (oral tablets) Usual dose: 50mg daily Efficacy highest in patients who can abstain for 4 to 7 days before initiating treatment No negative effect with use Some clients notice anxiolytic effect 40
  • 41. Long- Acting Naltrexone Brand name is Vivitrol Approved for alcoholism in 2006 Approved for opiate dependence Oct 2010 Given monthly, 380 mg appears to have increased efficacy versus 190 mg May have increased efficacy for men vs. women, and those abstinent when medication is initiated vs. those still drinking 41
  • 42. Long- Acting Naltrexone Discontinuation rate- 14% in patients on 380 mg a month, 7% in patients on 190 mg a month and placebo. Most common side effects: nausea, injection site reaction, headache. LFTs remained stable throughout the medication trial 42
  • 43. Naltrexone: Recent Research 2005: Cuts the relapse risk during first 90 days by 36% (28% relapse rate on oral naltrexone vs. 43% relapse rate on placebo) 2005: injectable naltrexone resulted in a 25% reduction in proportion of heavy drinking days vs. placebo Overall: helps to curb consumption in patients with multiple “slips” but less effective in maintaining abstinence 43
  • 44. Naltrexone Non-compliance is the main barrier to success Most useful for highly motivated patients w/ external circumstances • Impaired professionals, parolees, probationers, etc 44
  • 45. Methadone Opiate agonist to treat opiate dependence Well-studied and effective treatment • Normalizes function/return to work, decreases crime/violence, reduces HIV exposure Doses > 70mg/day generally better than low doses Enhanced services = improved outcomes • Counseling, medical, social/vocational services,etc No contraindication in SMI, though not well studied 45
  • 46. Methadone Usually taken once a day to suppress withdrawal for 24 to 36 hours Usually given in liquid form by Opiate Treatment Programs Induction phase—no more than 30 to 40 mg on the first day of treatment Dosage changes usually occur once a week • More rapid dosage increases can cause overdose Maintenance phase—usually 80-120mg daily 46
  • 47. Methadone Common side effects • Sweating, constipation, abnormal libido, sleep abnormalities, mild anorexia, weight gain, water retention Adverse effects • Prologation of QTc (usually seen with very high doses, mean of 350mg daily) 47
  • 48. Buprenorphine Opioid partial agonist  ↓ risk of overdose and ↓ abuse potential  May precipitate opiate withdrawal in dependent individuals Approved for treatment of opiate dependence • Maintenance dose in the range of 8-16 mg daily Sublingual route of administration  Subutex= Bup only; Suboxone= Bup + Naloxone 48
  • 49. Buprenorphine Approved in U.S. (2002) as office-based treatment vs. ‘methadone clinics’ Individual doctors may treat up to 30 patients at a time, using an special DEA # • After 1 year, may increase to 100 patients Must be addiction medicine/addiction psychiatry certified OR complete 8-hr training 49
  • 50. Direct Buprenorphine Induction from Short- Acting Opioids  Ask patient to abstain from short-acting opioid (e.g., heroin) for at least 6 hrs. and be in mild withdrawal before administering buprenorphine/naloxone.  When transferring from a short-acting opioid, be sure the patient provides a methadone-negative urine screen before 1st buprenorphine dose.SOURCE: Amass, et al., 2004, Johnson, et al. 2003.
  • 51. Buprenorphine Suboxone= buprenorphine + naloxone in a 4:1 mixture • Available doses: 8/2mg and 2/0.5mg • 2 sublingual forms: tablet and Film Induction phase Day 1: usual dose is 2 mg given every 2-3 hours, up to 8 mg Induction phase Day 2: start with 8mg, can go up to 16mg depending on patient symptoms 51
  • 52. Buprenorphine Maintenance phase: usually 8 to 16 mg daily This may vary in clinical practice, but realize that 16mg dose covers ~95% of opiate receptors Adverse side effects: Increased LFTs, cytolytic hepatitis Common side effects: generally mild • Constipation; dizziness; drowsiness; headache; nausea; sweating; vomiting; 52
  • 53. Buprenorphine: Recent Research The SAMHSA Evaluation of the Impact of the DATA Waiver Program • FINAL REPORT in March 2006 Buprenorphine clinically effective and well accepted by patients. Waiver Program has ↑ the availability of medication-assisted treatment for opioid addiction. Adverse effects, whether involving diversion or adverse clinical events or public health consequences, have been minimal. The 30-patient limit on individual physician practices and cost / reimbursement issues may be decreasing potential access to treatment. For more information, see www.buprenorphine.samhsa.gov 53
  • 54. Partial vs. Full Opioid Agonist deathOpiate Full Agonist (e.g., methadone)Effect Partial Agonist (e.g. buprenorphine) Antagonist (e.g. Naloxone) Dose of Opiate 54
  • 55. Possible Barriers to using MATPotential Fear # 1:  Rationale # 1:Medication will  Medication may be a eventually replace useful adjunct to rehabilitation as the treatment treatment of choice for  “Another tool in your addiction “a pill for toolbox” every ill” 55
  • 56. Possible Barriers to using MATPotential Fear # 2:  Rationale # 2:Medication will distract  Medication makes detox from the difficult work safer and more humane of recovery from  Medication may allow addiction the process of recovery to begin and continue  Medication may make recovery possible for those with severe mental illness 56
  • 57. Possible Barriers to using MATPotential Fear # 3:  Rationale # 3:Medication will perpetuate  Physical dependence to an existing addiction medication may occur, but addictive behavior should decreasePotential Fear # 4:  Rationale # 4:Medication will cause new  New addictions to addictions medications are a risk, but the actual incidence is quite low 57
  • 58. Other Barriers to MAT? Financial • MAT may be very expensive and many still do not have insurance Regulatory  Until very recently, doctor visits for MAT were not covered by ODADAS Logistical • Usual treatment settings may not be set up to provide MAT Others? 58
  • 59. Medications only work if… …they are getting “from the bottle to the bloodstream” How to help clients with the idea of starting meds? • “that will mean I am really sick…” OR “I don’t need a crutch…” How to help clients with the idea of staying on meds? • “I feel fine, I don’t need it anymore” OR “if I take meds, then I am not really sober”
  • 60. Some Lessons from Motivational Interviewing What are the client’s goals? How does medication fit (or not fit) with those goals? What are the pros and cons of the medications? Use of reflective listening What is the patient willing to do right now? What are the patient’s fears about medication?
  • 61. Hope for Recovery People with addictive disorders often lack experiences of success and have lost hope Medications in conjunction with other interventions can increase hope for a better life • Reduced symptoms of withdrawal • Reduced symptoms of craving • Support for long-term sobriety 61
  • 62. Resources “BUPRENORPHINE TREATMENT: A TRAINING FOR MULTIDISCIPLINARY ADDICTION PROFESSIONALS” • http://www.nida.nih.gov/blending/buptreatment.htm NIDA Methadone Research Web Guide http://international.drugabuse.gov/collaboration/PDFs/Me Mid-America Addiction Technology Transfer Center. Psychotherapeutic Medications 2011: What Every Counselor Should Know. http://www.mattc.org 62
  • 63. Contact InformationChristina M. Delos Reyes, MD Chief Clinical Officer ADAMHS Board of Cuyahoga County Phone: 216-241-3400 x 728 Fax: 216-241-0805 delosreyes@adamhscc.orgCenter for Evidence-Based Practices at Case www.centerforebp.case.edu