An overview of Medication Assisted Treatment (MAT) and acute pain management on MAT

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An overview of Medication Assisted Treatment (MAT) and acute pain management on MAT Goals of Discussion Recognize opioid use disorder (OUD) Discuss the pharmacology of medication assisted treatments (MAT) for OUD Describe principles acute pain control while on MAT Victoria Martineau, PharmD Patricia Pade, MD, FASAM Both authors have no disclosures OCTOBER 8, 2018 2 3 4 Response to opioid crisis Expanded access to Medication Assisted Therapy (MAT) o PAs and NP can now prescribe/increased limits on Office Based Opioid therapy o Expansion of telemedicine o ED initiation of treatment o Enhanced integration of behavioral health in primary care Promotion of harm reduction measures o Overdose education and naloxone for rescue Innovative use of community/peer support efforts Research in new formulations and medications o New formulations of buprenorphine Lessen opioid/controlled substance prescribing Opioid Use Disorder (OUD) 5 6 1

DSM-5 Criteria - OUD Opioids taken in larger amounts, longer than intended Unsuccessful efforts to cut down or control use A great deal of time spent obtaining, using or recovering from use Craving Recurrent use results in failure to fulfill work, home, school obligations Continued use resulting in interpersonal/social problems Recurrent use in hazardous situations SEVERITY: Important social, occupational or recreational activities Mild (2-3) are reduced due to use Moderate (4-5) Continues use despite knowledge of physical, psychological problems related to use Severe ( 6) Tolerance and withdrawal: NOT criteria if opioids are used solely under appropriate medical supervision Medication Assisted Therapy Withdrawal Normal Euphoria Acute Use Chronic Use Tolerance & Physical Dependence Medication Assisted Therapy 7 8 Full opioid agonist: Methadone μ μ receptor opioid Full agonist receptor Pharmacology of MAT Full agonist binding activates the μ opioid receptor Additive effect when combined with other full agonists Is highly reinforcing and has higher potential for abuse Abrupt discontinuation will result in withdrawal 9 10 Partial opioid agonist: Buprenorphine Opioid antagonists: Naloxone and Naltrexone μ receptor μ partial agonist opioid receptor Partial agonist binding activates the μ opioid receptor and kappa antagonist Competitive agonist with high binding affinity/slow disassociation Is less reinforcing than full agonists (lower risk for abuse) Abrupt discontinuation will result in withdrawal Available as sublingual, buccal, transdermal, and injection μ opioid receptor Antagonist binding to the μ opioid receptor occupies without activating Is not reinforcing μ receptor antagonist Blocks abused opioid agonist binding 11 12 2

Methadone Pharmacokinetics Buprenorphine Pharmacokinetics 13 14 15 16 Methadone and Buprenorphine as analgesics Both are approved for use in chronic pain Daily dosing used for MAT does not provide analgesia o Dosing frequency must be increased due to alpha/beta phases o Tolerance o Hyperalgesia Naltrexone Opioid antagonist o Binds competitively, but blocks opioid effect As oral tablet usual dose is 50 mg daily o t ½ = 14 hours, 50% blockade gone after 72 hours Comes in depo form 380 mg IM every 4 weeks o Peak plasma concentration in 2-3 days, declines in 1 days Blocks opioid analgesia blockade can be overcome with 6-20x the usual dose of opioids without significant respiratory depression 17 18 3

Obstacles to Good Care Acute Pain Control for Patients on MAT Providers: Bias and perception of OUD as moral failing, not a disease Physicians fear deception Lack of education about medications Providing MAT outside the mainstream of medicine Lack of good standards Patients: Fear of mistreatment Fear of being judged or labeled Fear of withdrawal Studies show: o Active opioid use disorder - less pain tolerance than matched controls o On MAT less pain tolerance o H/O of OUD have less pain tolerance than siblings without addiction. 19 20 General Principles Multi-modal pain control Opioid debt: Patients physically dependent on opioids (including methadone and buprenorphine) will need daily equivalence before an analgesic effect with opioids o Opioid analgesic requirements are often higher due to tolerance and increased pain sensitivity o Treating opioid withdrawal (which is painful) can improve pain management Giving opioids for pain will not create an addict in opioid dependent patients. Multi-Modal pain control Consider scheduled dosing for the following: Acetaminophen o Avoid combination opiate/apap products NSAIDs oral and topical Gabapentin Lidocaine patches Other agents: Ketamine Regional anesthesia Short-acting opioids Alford DP, Compton P, Samet JH. Ann Intern Med 2006 21 22 Opioid debt Opioid affinities for mu receptor MAT agents Short-acting opioids Opioids Range of Ki Value Levorphanol 0.19 to.23 32 Buprenorphine 0.21 to 1.5 Naltrexone 0.4 to 0.6 (antagonist effects) 20 Fentanyl 0.7 to 1.9 Methadone 0.72 to 5.6 Naloxone 1 to 3 (antagonist effects) 20 Morphine 1.02 to 4 Pentazocine 3.9 to 6.9 Codeine 65 to 135 Table 5. Mu Receptor Affinities of Various Opioids 19 23 24 4

Macintyre PE et al, Pain relief and opioid requirements in the first 24 hours after surgery in patients taking buprenorphine and methadone opioid substitution therapy; Anaesth Intensive Care 2013; 41:222-230 Methadone Contact methadone clinic dosing will not appear in PMP o Verify current dose AND date of last administration Consider continuing outpatient dosing o Split total daily dose TID to address pain o Add short-acting opiates side effects will be additive and patients will be tolerant When to reduce methadone dose (10-20% reduction in TDD): o Respiratory failure o Somnolence o QTc >500 o Concurrent benzodiazepine Avoid if possible Buprenorphine Analgesic efficacy of buprenorphine Consider continuing outpatient dosing o Split total daily dose TID to address pain o Add short-acting opiates if necessary higher doses are required to overcome binding affinity o Avoid risk of overdose on other opiates during buprenorphine discontinuation o Avoid risk of relapse o Avoid the need to re-induce 27 The clinical analgesic efficacy of buprenorphine, Volume: 39, Issue: 6, Pages: 577-583, First published: 29 July 2014, DOI: (10.1111/jcpt.12196) Naltrexone Recommend: Oral: wait 72 hours before surgery IM: schedule surgery at end of cycle Must overcome blockade, but also loss of tolerance Restart naltrexone once abstinent from opioids (depending on length of time) Use multi-modal approach for pain control and opioid sparing. If acute pain service available, would consult. Case 1 45 year old woman admitted with a broken femur. She has a history of diabetes and Hepatitis C. She says that she takes methadone 120 mg daily and has been attending a methadone clinic for 1 year. This is her second hospital day. 29 30 5

General Principles PMP check Urine drug screening Pregnancy test for women of child-bearing age Use of non-opioid treatments Confirm dosing at the methadone clinic Inpatient Addiction Medicine Service 31 32 Methadone Clinic Contact Record Methadone clinic name How long attending clinic What is the daily dose and when did they last dose Do they have take homes What is the patient s compliance We include the following statement on our record: Case 2 35 year old man who is admitted for RLQ pain. Diagnosed with appendicitis and has surgery. He has been on Buprenorphine/naloxone 8 mg a day for 9 months and reports no heroin use since starting the medication. He took his dose the the day of admission. You are asked to see him the following day. If no dose taken in past 2-5 days, give ½ dose first day, dosing advance cautiously as clinically appropriate and/or in collaboration with addiction medicine or the methadone clinic If no dose taken for >5 days, requires further medical evaluation - consult addiction medicine or the methadone clinic. 33 34 Case 3 62 year old male patient who has been treated for his OUD successfully with naltrexone 50 mg qd for 6 years. He needs to be admitted for a knee replacement. Recovery Support Stress, pain, insomnia, illness, isolation are major triggers for relapse. Important to understand what recovery supports patient has in place, and what recovery supports may be needed. Help patient utilize the tools acquired in treatment. - Coping skills - Relaxation techniques - Mindfulness 12 step sponsor support, Big Book Relapse prevention strategies 35 36 6

References Alford DP et al, Ann Intern Med 2006; 144(2) 127-134 Alford DP, Handbook of Office Based Buprenorphine Treatment 2010 Coffa D, Acute Pain and Perioperative Management in OUD, SHOUT 2017 Early P et al, Acute pain episode outcomes in patients on extended naltrexone 2013 Kornfeld H and Manfredi, Am J Therapeutics 2010 Macintyre PE et al Anesth Intensive Care 2013 Merrill JO et al. J Gen Intern Med 2002 Oifa S et al Clin Ther 2009 Raffa et al J of Clinical Pharm and Therapeutics 2014 39 577-583 37 7