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Review ArticleClinical Review

Opioid Analgesics in Primary Care: Challenges and New Advances in the Management of Noncancer Pain

Raymond Sinatra
The Journal of the American Board of Family Medicine March 2006, 19 (2) 165-177; DOI: https://doi.org/10.3122/jabfm.19.2.165
Raymond Sinatra
MD, PhD
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    Mean steady-state plasma concentration of oxymorphone immediate release 10 mg and oxymorphone extended release 20 mg.32, 33

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    Table 1.

    General Dos and Don’ts Regarding the Use of Opioid Therapy in Patients with Chronic Noncancer Pain

    DoDon’t
    Consider opioids only after all other reasonable attempts at analgesia have failedForget to evaluate patients (ie, history and physical examination)
    Recognize that a history of substance abuse, severe character pathology, and chaotic home environment are contraindicationsInitiate treatment without first establishing a diagnosis
    Ensure that the primary responsibility for treatment is assumed by a single practitionerForget to obtain outside medical records or to talk with previous practitioners (any verification at all)
    Obtain informed consent from the patient before initiating therapyPrescribe treatment without establishing specific goals (ie, reduction in pain, improvement in function)
    Prescribe doses on an around-the-clock basisFail to screen for addictive potential and monitor patient through treatment
    Reassess if failure to achieve at least partial analgesia at relatively low initial doses in the nontolerant patientFail to document the diagnosis, treatment plan, goals for treatment, continuing need for medication, and laboratory results
    Emphasize gains in physical and social functionFail to understand what drug testing can and cannot tell you
    Permit patients to transiently escalate dose on days of increased painDeviate from the ‘contract’ (ie, misbehavior is never addressed either verbally or written)
    See patients and prescribe drugs at least monthly, at least in the initial phases of treatmentAccept blindly whatever is said by the patient
    Manage exacerbations of pain in the hospital, where dose escalation can be observed and the dose returned to baselineAttempt to bully law enforcement or regulatory agents, or assume an arrogant ‘I-know-best’ attitude when confronted by them
    Assess patients for evidence of drug hoarding, acquisition of drugs, uncontrolled dose escalation, or other aberrant behaviors
    Incorporate comfort, side effects, functional status, and existence of aberrant drug-related behaviors into pain assessment at each visit
    Consider use of self-reporting instruments, an example of which is shown in Table 2
    Remember that documentation is essential and should address all elements of the visit assessment
    • Adapted with permission from Portenoy28 and Gallagher.18

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    Table 2.

    Items on the Screener and Opioid Assessment for Patients With Pain (SOAPP) Questionnaire

    ItemConcept Domain
    How often do you feel that your pain is out of control?Neurobiologic need for medicine
    How often have you felt a need for higher doses of medication to treat your pain?Neurobiologic need for medicine
    How often have you felt a craving for medication?Neurobiologic need for medicine
    How often do you take more medication than you are supposed to?Medication-related behaviors
    How often have you taken medication other than the way that it was prescribed?Medication-related behaviors
    How often have your medications been lost or stolen?Medication-related behaviors
    How often have others expressed concern over your use of medication?Medication-related behaviors
    How often has more than one doctor prescribed pain medication for you at the same time?Antisocial behaviors
    How often, in your lifetime, have you had legal problems or been arrested?Antisocial behaviors
    How often do you smoke a cigarette within an hour after you wake up?Substance abuse history
    How often have any of your family members, including parents and grandparents, had a problem with alcohol or drugs?Substance abuse history
    How often have any of your close friends had a problem with alcohol or drugs?Substance abuse history
    How often have others suggested that you have a drug or alcohol problem?Substance abuse history
    How often have you attended an AA or NA meeting?Substance abuse history
    How often have you been treated for an alcohol or drug problem?Substance abuse history
    How often have you used illegal drugs (for example, marijuana, cocaine, etc.) in the past 5 years?Substance abuse history
    How often do you have mood swings?Psychiatric history
    How often have you been seen by a psychiatrist or a mental health counselor?Psychiatric history
    How often do you do things that you later regret?Psychosocial problems
    How often has your family been supportive and encouraging?Psychosocial problems
    How often have others told you that you have a bad temper?Psychosocial problems
    How often have you had a problem getting along with the doctors who prescribed your medicines?Doctor-patient relationship
    How often have you been asked to give a urine screen for substance abuse?Doctor-patient relationship
    Compared with other people, how often have you been in a car accident?Personal care/lifestyle
    • AA, Alcoholic’s Anonymous; NA, Narcotics Anonymous.

    • Adapted with permission from Butler et al.25

    • View popup
    Table 3.

    Opioids and Other Medications Metabolized by CYP2D6 and CYP3A4 Enzymes

    EnzymesOpioidsPopular Medications/ Substrates
    CYP2D6CodeineCarvedilol
    DextromethorphanPropafenone
    DihydrocodeineAmitriptyline
    OxycodoneParoxetine
    TramadolRisperidone
    Thioridazine
    Fluoxetine
    Lidocaine
    Nortriptyline
    Propranolol
    Tamoxifen
    Venlafaxine
    CYP3A4BuprenorphineClarithromycin
    FentanylErythromycin
    MethadoneAlprazolam
    OxycodoneCyclosporine
    Chlorpheniramine
    Diltiazem
    Lovastatin
    Hydrocortisone
    Buspirone
    Caffeine
    Nifedipine
    Verapamil
    Diazepam
    • Data from Flockhart57 and Lalovic et al.58

    • View popup
    Table 4.

    Dose Administration Data for Commonly Used Opioid Analgesics

    DrugApproximate Equianalgesic Oral DoseApproximate Equianalgesic Parenteral DoseRecommended Starting Dose (Adults >50 kg Body Weight)
    OralParenteral
    Morphine20–60 mg/day initial starting dose; then 30 mg q3-h (IR)10 mg q3–4 hours30 mg q3–4 hours*10 mg q3–4 hours (use of IV route is preferable)
    Fentanyl0.1†
    Oxycodone30 mg q3–4 hours (IR)NA10 mg q3–4 hoursNA
    Hydromorphone‡7.5 mg q3–4 hours1.5 mg q3–4 hours6 mg q3–4 hours1.5 mg q3–4 hours
    Methadone5–10 mg q6–8 hours5–10 mg q6–8 hours5–10 mg q6–8 hours2.5–5 mg q6–8 hours
    • IR, immediate release; IV, intravenous; NA, not available.

    • * Starting dose of 20 to 60 mg/day may be used to avoid adverse effects such as vomiting.

    • † Transdermal fentanyl 100 μg/hr is approximately equivalent to 2 to 4 mg/hr of IV morphine. A conversion factor for transdermal fentanyl that can be used for equianalgesic calculation is 17 μg/hr. Roughly, the dose of transdermal fentanyl in μg/hr is approximately one-half of the 24-hour dose of oral morphine.

    • ‡ For morphine and hydromorphone, rectal administration is an alternate route for patients unable to take oral medication, but equianalgesic doses may differ from oral and parenteral doses because of pharmacokinetic differences.

    • Reprinted with permission from Nicholson.8

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The Journal of the American Board of Family Medicine: 19 (2)
The Journal of the American Board of Family Medicine
Vol. 19, Issue 2
March-April 2006
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Opioid Analgesics in Primary Care: Challenges and New Advances in the Management of Noncancer Pain
Raymond Sinatra
The Journal of the American Board of Family Medicine Mar 2006, 19 (2) 165-177; DOI: 10.3122/jabfm.19.2.165

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Opioid Analgesics in Primary Care: Challenges and New Advances in the Management of Noncancer Pain
Raymond Sinatra
The Journal of the American Board of Family Medicine Mar 2006, 19 (2) 165-177; DOI: 10.3122/jabfm.19.2.165
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