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Identify the negative impact of chronic pain on health and quality of life, current methods to assess pain levels, appropriate use of opioid medications, and documentation required for compliance with regulatory policiesIntegrate appropriate risk assessment strategies for patient abuse, misuse, and
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1. Practical Issues in Chronic Pain: Managing Analgesia in thePrimary Care Setting
2. Identify the negative impact of chronic pain on health and quality of life, current methods to assess pain levels, appropriate use of opioid medications, and documentation required for compliance with regulatory policies
Integrate appropriate risk assessment strategies for patient abuse, misuse, and diversion among opioid therapies into an overall management approach for chronic pain
Describe the specific elements of new abuse deterrent technologies associated with opioid therapy and assess their implications for clinical practice
Educational Learning Objectives
4. Multiple Types of Pain
5. Case Study 1 A 56-year-old healthy male with chronic back pain
Spinal stenosis after auto accident (age 45)
Negative for OP
Conservative therapy ineffective
Persistent pain 6/10 and activity related pain 10/10
ORT 5
UDT consistent therapy
PMP: no opioids
Rx started with hydrocodone 10 mg/APAP q 4 hours
Titrated to 50 mg CR morphine/naltrexone BID Slide 64 is an alternative version of this slide. Instead of the last 2 bullet points, the audience is given an open-ended question to encourage participation in the case. Slide 64 is an alternative version of this slide. Instead of the last 2 bullet points, the audience is given an open-ended question to encourage participation in the case.
6. Long-Term Consequences of Acute Pain: Potential for Progression to Chronic Pain
7. Neuroplasticity in Pain Processing
8. Vicious Cycle of Uncontrolled Pain
9. Breaking the Chain of Pain Transmission
10. Multimodal Treatment
11. Components of Chronic Pain Chronic pain
Baseline persistent pain
Breakthrough pain (BTP)
Each component of chronic pain needs to be independently assessed and managed
12. Monitoring
Weekly visits until stable
Prescribe only enough medication until next visit
Rx
Short acting for BTP
CR formulation (with less street attractiveness)
Six month follow-up
Difficulty sleeping
No aberrant behaviors
PMP showed no aberrant behavior
Monthly Urine Drug Test (UDT) consistent with therapy
Transferred to dextropropoxyphene/acetaminophen 10 /day
13. Positioning Opioid Therapyfor Persistent Pain Chronic non-cancer pain: evolving perspective
Consider for all patients with severe chronic pain, but weigh the influences
What is conventional practice?
Are there reasonable alternatives?
What is the risk of adverse events?
Is the patient likely to be a responsible drug-taker?
14. Chronic Opioid Therapy Guidelines
15. Chronic Opioid Therapy Guidelines
16. Opioid Formulations
17. Formulation Points to Consider
Dose-limiting issues and toxicity with co-analgesics
4 g/day acetaminophen limit
Importance of titration
Risk of overdose, challenges of dose conversion during rotation
Pharmacokinetics versus temporal patterns of pain
Adherence
Cost
Convenience
Caregiving issues
18. Domains for Pain Management Outcome: The 4 A’s Analgesia
Activities of Daily Living
Adverse Events
Aberrant Drug-Taking Behaviors
19. Model Policy for the Use of Controlled Substances for the Treatment of Pain Federation of State Medical Boards House of Delegates, May 2004. http://fsmb.org. Accessed March 2010.
20. FSMB Model PolicyBasic Tenets
21. New Illicit Drug Use United States, 2006
22. Definition of Terms
23. Prevalence of Misuse, Abuse, and Addiction
24. Who Misuses/Abuses Opioids and Why?
25. Rx Opioid Users Are Heterogeneous SUD = Substance Use DisorderSUD = Substance Use Disorder
26. Risk Factors for Aberrant Behaviors/Harm
27. Stratify Risk
28. 10 Principles of Universal Precautions
Diagnosis with appropriate differential
Psychological assessment including risk of addictive disorders
Informed consent (verbal or written/signed)
Treatment agreement (verbal or written/signed)
Pre-/post-intervention assessment of pain level and function
Appropriate trial of opioid therapy adjunctive medication
Reassessment of pain score and level of function
Regularly assess the “Four A’s” of pain medicine: Analgesia, Activity, Adverse Reactions, and Aberrant Behavior
Periodically review pain and comorbidity diagnoses, including addictive disorders
Documentation Universal precautions revisited: managing the inherited pain patient.
Gourlay DL, Heit HA.
Pain Med. 2009 Jul;10 Suppl 2:S115-123.
Universal precautions in pain medicine: a rational approach to the treatment of chronic pain.
Gourlay DL, Heit HA, Almahrezi A.
Pain Med. 2005 Mar-Apr;6(2):107-112.Universal precautions revisited: managing the inherited pain patient.
Gourlay DL, Heit HA.
Pain Med. 2009 Jul;10 Suppl 2:S115-123.
Universal precautions in pain medicine: a rational approach to the treatment of chronic pain.
Gourlay DL, Heit HA, Almahrezi A.
Pain Med. 2005 Mar-Apr;6(2):107-112.
29. Initial Visits Initial comprehensive evaluation
Risk assessment
Prescription monitoring assessment
Urine drug test
Opioid treatment agreement
Opioid consent form
Patient education
30. Principles of Responsible Opioid Prescribing Patient Evaluation
Assessment and history
Directed physical exam
Personal and family history of substance abuse/psychiatric problems
Assessment of comorbidities
Accurate record keeping
31. Principles of Responsible Opioid Prescribing Treatment Plan
I have resolved key points before initiating opioid therapy
Diagnosis established and opioid treatment plan developed
Established level of risk
I can treat this patient alone/I need to enlist other consultants to co-manage this patient (pain or addiction specialists)
I have considered nonopioid modalities
Pain rehabilitation program
Behavioral strategies
Non-invasive and interventional techniques
32. Principles of Responsible Opioid Prescribing Treatment Plan (cont)
Drug selection, route of administration, dosing/dose titration
Managing adverse effects of opioid therapy
Assessing outcomes
Written agreements in place outlining patient expectations/responsibilities
Consultation as needed
Periodic review of treatment efficacy, side effects, aberrant drug-taking behaviors
33. Medical Records Maintain accurate, complete, and current records
Medical Hx & PE
Diagnostic, therapeutic, lab results
Evaluations/consultations
Treatment objectives
Discussion of risks/benefits
Tx and medications
Instructions/agreements
Periodic reviews
Discussions with and about patients
34. Opioid Treatment Agreement http://www.lni.wa.gov/ClaimsIns/Files/OMD/agreement.pdfhttp://www.lni.wa.gov/ClaimsIns/Files/OMD/agreement.pdf
35. Differential Diagnosis of Aberrant Drug-Taking Attitudes and Behavior Addiction (out-of-control, compulsive drug use)
Pseudoaddiction (inadequate analgesia)
Other psychiatric diagnosis
Organic mental syndrome (confused, stereotyped drug-taking)
Personality disorder (impulsive, entitled, chemical-coping behavior)
Chemical coping (drug overly central)
Depression/anxiety/situational stressors (self-medication)
Criminal intent (diversion)
36. Identifying Who Is at Risk for Opioid Abuse and Diversion Predictive tools
Aberrant behaviors
Urine drug testing
Prescription monitoring
programs
Severity and duration of pain
Pharmacist communication
Family and friends
Patients
37. Signs of Potential Abuse and Diversion Request appointment toward end-of-office hours
Arrive without appointment
Telephone/arrive after office hours when staff are anxious to leave
Reluctant to have thorough physical exam, diagnostic tests, or referrals
Fail to keep appointments
Unwilling to provide past medical records or names of HCPs
Unusual stories
38. ORT Validation
39. Current Opioid Misuse Measure (COMM) Butler SF, Budman SH, Fernandez KC, et al. Development and validation of the Current Opioid Misuse Measure.
Pain. 2007;130(1-2):144-156.
Clinicians recognize the importance of monitoring aberrant medication-related behaviors of chronic
pain patients while being prescribed opioid therapy. The purpose of this study was to develop and
validate the Current Opioid Misuse Measure (COMM) for those pain patients already on long-term
opioid therapy. An initial pool of 177 items was developed with input from 26 pain management and
addiction specialists. Concept mapping identified six primary concepts underlying medication
misuse, which were used to develop an initial item pool. Twenty-two pain and addiction specialists
rated the items on importance and relevance, resulting in selection of a 40-item alpha COMM. Final
item selection was based on empirical evaluation of items with patients taking opioids for chronic,
noncancer pain (N=227). One-week test-retest reliability was examined with 55 participants. All
participants were administered the alpha version of the COMM, the Prescription Drug Use
Questionnaire (PDUQ) interview, and submitted a urine sample for toxicology screening. Physician
ratings of patient aberrant behaviors were also obtained. Of the 40 items, 17 items appeared to
adequately measure aberrant behavior, demonstrating excellent internal consistency and test-retest
reliability. Cutoff scores were examined using ROC curve analysis and reasonable sensitivity and
specificity were established. To evaluate the COMM’s ability to capture change in patient status, it
was tested on a subset of patients (N = 86) that were followed and reassessed three months later. The
COMM was found to have promise as a brief, self-report measure of current aberrant drug-related
behavior. Further cross-validation and replication of these preliminary results is pending.Butler SF, Budman SH, Fernandez KC, et al. Development and validation of the Current Opioid Misuse Measure.
Pain. 2007;130(1-2):144-156.
Clinicians recognize the importance of monitoring aberrant medication-related behaviors of chronic
pain patients while being prescribed opioid therapy. The purpose of this study was to develop and
validate the Current Opioid Misuse Measure (COMM) for those pain patients already on long-term
opioid therapy. An initial pool of 177 items was developed with input from 26 pain management and
addiction specialists. Concept mapping identified six primary concepts underlying medication
misuse, which were used to develop an initial item pool. Twenty-two pain and addiction specialists
rated the items on importance and relevance, resulting in selection of a 40-item alpha COMM. Final
item selection was based on empirical evaluation of items with patients taking opioids for chronic,
noncancer pain (N=227). One-week test-retest reliability was examined with 55 participants. All
participants were administered the alpha version of the COMM, the Prescription Drug Use
Questionnaire (PDUQ) interview, and submitted a urine sample for toxicology screening. Physician
ratings of patient aberrant behaviors were also obtained. Of the 40 items, 17 items appeared to
adequately measure aberrant behavior, demonstrating excellent internal consistency and test-retest
reliability. Cutoff scores were examined using ROC curve analysis and reasonable sensitivity and
specificity were established. To evaluate the COMM’s ability to capture change in patient status, it
was tested on a subset of patients (N = 86) that were followed and reassessed three months later. The
COMM was found to have promise as a brief, self-report measure of current aberrant drug-related
behavior. Further cross-validation and replication of these preliminary results is pending.
40. Urine Drug Testing (UDT) General drug tests only detect nonsynthetic substances, such as morphine
Specific tests for synthetic drugs must be requested
41. Detection of Opioids Opiate immunoassays detect morphine and codeine
Do not detect synthetic opioids
Methadone
Fentanyl
Do not reliably detect semisynthetic opioids
Oxycodone
Hydrocodone
Buprenorphine
Hydromorphone
GC/MS will identify these medications
42. The Role of UDT UDT in clinical practice may
Provide objective documentation of compliance with treatment plan by detecting presence of a particular drug or its metabolites
Assist in recognition of addiction or drug misuse if results abnormal
Results are only as reliable as testing laboratory’s ability to detect substance in question
43. Positive forensic testing
Legally prescribed medications
Over-the-counter medications
Illicit drugs or unprescribed medications
Substances that produce the same metabolite as that of a prescribed or illegal substance
Errors in laboratory analysis Negative compliance testing
Medication bingeing
Diversion
Insufficient test sensitivity
Failure of laboratory to test for desired substances
Positive and Negative Urine Toxicology Results
44. Detection Times of Common Drugs of Misuse
45. Risk Evaluation and Mitigation Strategies Position of the FDA
The current strategies for intervening with [the problem of prescription opioid addiction, misuse, abuse, overdose and death] are inadequate
New authorities granted under FDAAA: [FDA] will now be implementing Risk Evaluation and Mitigation Strategies (REMS) for a number of opioid products
[FDA expects] all companies marketing these products to [cooperate] to get this done expeditiously
If not, [FDA] cannot guarantee that these products will remain on the market
46. Identifying and Managing Abuse and Diversion
Assessing risk and aberrant behaviors
Performing scheduled and random UDTs
Utilization of PMPs
Assessing stress and adequacy of pain control
Developing good communication with pharmacists
Receiving input from family, friends, and other patients
48. Physical Deterrent: Viscous Gel Base SR oxycodone formulation: Remoxy®
Deters dose dumping
Accessing entire 12-h dose of CR medication at 1 time
Difficult to crush, break, freeze, heat, dissolve
The viscous gel-cap base of PTI-821 cannot be injected
Resists crushing and dissolution in alcohol or water
49. Aversive Component Capsaicin
– Burning sensation
Ipecac
– Emetic
Denatonium
– Bitter taste
Niacin
– Flushing, irritation
50. Pharmacologic Deterrent: Antagonist Oral formulation
Sequestered antagonist
Antagonist bioavailable only when agent is crushed for extraction
SR morphine + naltrexone (Embeda®) FDA approved 2009
51. Remaining Questions How much does the barrier approach deter the determined abuser?
How much do agonist/antagonist compounds retain efficacy?
How much do agonist/antagonist compounds pose serious adversity?
52. Case Study 2 A recently widowed 72-year-old female with severe osteoarthritis of hips and knees has been having increasing difficulty ambulating due to pain
She had been taking over-the-counter NSAIDs for the pain but developed an upper GI bleed
She resides with her unmarried son who has a history of substance abuse
Quit smoking 40 years ago, drinks occasional glass of wine
Has been taking duloxetine for anxiety and depression
Upon discharge from the hospital she was given a prescription for acetaminophen/codeine but stopped taking the prescription due to severe constipation
53. Case Study 2 (cont) Rx
Multimodal therapy included osteopathic manipulation and physical therapy for gait training, progressive exercise program, and aquatherapy
Lidocaine 5% patches were prescribed
Two weeks later
She appears to be more ambulatory but still rates the pain in her hips and knees as 7/10 per NRS
Is she a candidate for opioid therapy?
Which opioid, what delivery system?
54. Conclusion
55. Pharmacovigilance
Functional outcomes
Standard medical practice
FSMB policy
Open Issues
What is meant by pain management?
Who needs what treatment?
Do universal approaches work?
Does it improve outcomes?
For patients
For regulators
57. Online Resources Melzack R. The McGill Pain Questionnaire. In: Pain Measurement and Assessment. New York:Raven Press, 1983, 41-48.
Melzack, R. The short-form McGill Pain Questionnaire. Pain 1987;30:191-7.
OTA: see Gourlay? Passik? Melzack R. The McGill Pain Questionnaire. In: Pain Measurement and Assessment. New York:Raven Press, 1983, 41-48.
Melzack, R. The short-form McGill Pain Questionnaire. Pain 1987;30:191-7.
OTA: see Gourlay? Passik?
58. McGill Short Form Pain Questionnaire The short-form McGill Pain Questionnaire (SF-MPQ). Descriptors 1-11 represent the sensory dimension of pain experience and 12-15 represent the affective dimension. Each descriptor is ranked on an intensity scale of 0 = none, 1 = mild, 2 = moderate, 3 = severe. The Present Pain Intensity (PPI) of the standard long-form McGill Pain Questionnaire (LF-MPQ) and the visual analogue (VAS) are also included to provide overall intensity scores.
The short-form McGill Pain Questionnaire (SF-MPQ). Descriptors 1-11 represent the sensory dimension of pain experience and 12-15 represent the affective dimension. Each descriptor is ranked on an intensity scale of 0 = none, 1 = mild, 2 = moderate, 3 = severe. The Present Pain Intensity (PPI) of the standard long-form McGill Pain Questionnaire (LF-MPQ) and the visual analogue (VAS) are also included to provide overall intensity scores.
59. Initiation of Therapy for Chronic Pain
60. Current Opioid Misuse Measure (COMM)
61. Monitoring Chronic PainReview of Efficacy of Therapy
62. Alternative to Slide 6:
63. Case Study 1 A 56-year-old healthy male with chronic back pain
Spinal stenosis after auto accident (age 45)
Negative for OP
Conservative therapy ineffective
Persistent pain 6/10 and activity related pain 10/10
ORT 5
UDT consistent therapy
PMP: no opioids
Plans? This patient was treated in the following way:
Rx started with hydrocodone 10 mg/APAP q 4 hours
Titrated to 50 mg CR morphine/naltrexone BID
This patient was treated in the following way:
Rx started with hydrocodone 10 mg/APAP q 4 hours
Titrated to 50 mg CR morphine/naltrexone BID