Chronic Pain: to prescribe or not to prescribe...Meta-analysis of 41 RCTs; duration 16 weeks; pain...
Transcript of Chronic Pain: to prescribe or not to prescribe...Meta-analysis of 41 RCTs; duration 16 weeks; pain...
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Chronic Pain:to prescribe or not to
prescribe
Lori Montgomery MD CCFPMedical Director, Chronic Pain Centre
Clinical Lecturer, Family Medicine and Anesthesia
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Disclosure of Conflict of Interest
• No conflicts to report
• No:– Grants
– Consulting fees
– Other
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Objectives
1) Recognize the role of medication in chronic pain management;
2) Comprehend the current situation within Alberta (both regarding medical marijuana and the prevalence of prescription drug abuse/misuse);
3) Identify patients that would benefit from de-prescribing and alternatives.
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Tissue damageInflammationNerve compression
5-HT, Bradykinin, Cytokines,Histamine, Prostaglandins
The Chemistry of Pain
EAAs NMDA receptors SubP / NGF / NK1 / CGRP / NO
Neuronal Plasticity
Descending Excitation /Inhibition
Dynorphin A / CCK 5HT / NE / GABA
AttentionExpectation
Affect
Peripheral Sensitization Central
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Montgomery 2013, Adapted from Twycross R, et al. Palliative Care Formulary. Radcliffe Medical Press, Oxford; 1998:86
Acetaminophen
NSAIDsCOXIBs
BuprenorphineTramadol
AntidepressantsAnticonvulsantsCannabinoids
CodeineMorphineOxycodoneHydromorphoneFentanylMethadone
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Canada 753mg/capitaUS 693 mg/capita
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Local context
30 million high dose Rx dispensed in Canada/ yearAlberta 2nd highest MEDD in CanadaCalgary has the highest overdose rate in Alberta
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ED Visits – Combined
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http://calgaryherald.com/news/crime/calgary-man-charged-with-smuggling-fentanyl-from-china
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Do they work?
Opioid Therapy for Chronic Pain. Jane C. Ballantyne, M.D., and Jianren Mao, M.D., Ph.D. N Engl J Med 2003;349:1943-53.
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Efficacy
Meta-analysis of 15 RCTs; duration 4-6 weeks; pain intensity (including NeP) reduced by about 30%
Kalso et al, Pain 2004
Meta-analysis of 8 RCTs in NeP; duration <28 days; significant benefit
Eisenberg et al, JAMA 2005
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EfficacyMeta-analysis of 41 RCTs; duration 16 weeks; pain intensity reduced with strong opioids, not with weak or non-opioids; more than 1/3 abandoned treatment for lack of efficacy
Furlan et al, CMAJ 2006
Meta-analysis of 6 RCTs in LBP; duration <16 weeks; no significant reduction in pain intensity
Martell et al, Ann Intern Med 2007
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In OA, research demonstrating long-term improvements in pain/function is lacking. In elderly patients with OA, the risk of opioids may be even greater than the risk of NSAIDs. Opioids should not be routinely used in OA; if necessary, they should be used for short-courses in carefully selected patients.
Ivers, Dhalla, Allan, TFP ACFP 2012
Efficacy
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Smith, HS. Pain Physician, 2012;15:ES1-ES7
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The down side
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the patient may have no other tools to use
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The patient isn’t alone
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We do have some influence
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Opioid tapering
Explain Pain and role of medicationsMotivational interviewing approach to changeTeam support, planSlow, structured taper
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Reinforce patient’s motivation
Make sure the patient knows what to expect – and troubleshoot ahead of time
Try to avoid alternative Rx
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Opioid tapering
Scheduled, ideally low dose tabletsBlister pack, weekly dispensing10% per week to startAgree to plateau if needed, but not go back up
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Clearly proven risks and benefits for pain patients
Bostwick JM, Blurred boundaries: the therapeutics and politics of medical marijuana, Mayo Clinic Proceedings 87.2 (Feb. 2012): p172.
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Neuropathic painFibromyalgiaBack painHIV neuropathyMS painMuscle spasmMyofascial painPelvic painMigraineTension headache
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CFPC guidance
There is no evidence to support use of marijuana for fibromyalgia, back pain, OA
Should be considered only for neuropathic pain that has failed to respond to standard treatments, including pharmaceutical cannabinoids
Should not be used for sleep or anxiety
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Evidence to dateAbrams, D. I., Jay, C. A., Shade, S. B., Vizoso, H. and others. (2007). Cannabis in painful HIV-associated sensory neuropathy: a randomized placebo-controlled trial. Neurology. 68: 515-521.
Wilsey, B., Marcotte, T., Tsodikov, A., Millman, J. and others. (2008). A randomized, placebo-controlled, crossover trial of cannabis cigarettes in neuropathic pain. J.Pain. 9: 506-521.
Ellis RJ, Toperoff W, Valda F, van den Brande G and others. Smoked medicinal cannabis for neuropathic pain in HIV: a randomized, crossover clinical trial. Neuropsychopharmacology. 34(3): 672-80 (2009)
Ware MA, Wang T, Shapiro S, Robinson A, Ducruet T, Huynh T, Gamsa A, Bennett GJ, Collet JP, Smoked cannabis for chronic neuropathic pain: a randomized controlled trial, CMAJ 182(14): E694-701 (2010)
Wilsey, B., Marcotte, T., Deutsch, R., Gouaux, B. et al. Low-Dose Vaporized Cannabis Significantly Improves Neuropathic Pain. J.Pain. 14: 136-148 (2012)
Wallace MS, Marcotte TD, Umlauf A, Gouaux B, and Atkinson JH, Efficacy of Inhaled Cannabis on Painful Diabetic Neuropathy, The Journal of Pain, Vol16(7): 616-627 (2015)
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Evidence to dateAverage N=30
Duration of studies ≤5 days
All previous smokers of marijuana
Amounts ranging 25mg-900mg
THC ≤9.4%One study 20% not an efficacy study, n=8
Smoking or vapourizing
Reduction in pain ranging from 0.7 to 3 points on the NRS
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Evidence of risks
Volkow ND, Baler RD, Compton WM, Weiss SRB, Adverse Health Effects of Marijuana Use, N Engl J Med 2014;370:2219-27.
Li MC, Brady JE, DiMaggio CJ, Lusardi AR, TzongKY, Li G, Marijuana Use and Motor Vehicle Crashes, Epidemiologic Reviews, Vol. 34, 2012
Crane NA, Schuster RM, Fusar-Poli P, Gonzalez R, Effects of Cannabis on Neurocognitive Functioning: Recent Advances, Neurodevelopmental Influences, and Sex Differences, Neuropsychol Rev (2013) 23:117–137
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Evidence of risksCannabis Use Disorder
Mood
Cognitive impairmentDrivingPregnancyChildren and adolescents
COPD
Cardiovascular/hepatic
Hyperemesis
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CFPC guidance
Do not authorize:Under age 25Personal or strong family history of psychosisCurrent or past cannabis use disorderCardiovascular or respiratory diseasePregnant or breastfeeding
? Hepatic disease
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CFPC guidance
Use caution:Active mood or anxiety disorderSmoke tobaccoRisk factors for cardiovascular diseaseHeavy users of alcohol or taking high doses of opioids or benzodiazepines or other sedating medications
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Lay the groundworkDocument consent discussion and patient education
Document risk assessment, UDT and cannabis treatment agreement
Document concrete, measurable functional goals
Agree that treatment will be stopped if function does not improve
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Ongoing monitoring
Function
Adverse effects
Evidence of cannabis use disorder
(as best you can) Aberrant medication behaviour
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Process (very briefly)Be familiar with CPSA Standard of Practice
Email CPSA to let them know you will be authorizing
Ask patient to choose a licensed producer
Complete the Medical Document and send it directly to the LP
Patient registers with the LP and purchases their product, which is couriered to them directly
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ReferencesFranklin GM. Opioids for chronic noncancer pain: a position paper of the American Academy of Neurology. Neurology 2014;83:1277-84.
Eriksen J et al. Critical issues on opioids in chronic non-cancer pain: an epidemiological study. Pain 2006;125:172-9.
Gomes T et al. Trends in high-dose opioid prescribing in Canada. Can Fam Physician 2014;60:826-32
Gale J. A practical guide to health behaviour change using the HCA approach. Health Change Associates. Canadian Edition, 2012.
National Opioid Use Guideline Group. (2010). Canadian guideline for safe and effective use of opioids for chronic non-cancer pain. Retrieved from http://nationalpaincentre.mcmaster.ca/opioid/