Chronic pain is a widespread, costly condition that influences every aspect of normal functioning ; collectively, pain imposes a greater economic burden than any other disease, with estimates of annual cost near $300 billion. Opioids have been used to relieve pain for thousands of years, and prescription opioid medications continue to be a very common treatment modality for chronic non–cancer-related pain. Simultaneously, prescription opioid medications used for nonmedical purposes have rapidly become common drugs of abuse and the most likely cause of unintentional overdose. As a result, the relationship between pain and addiction is a complicated one that poses several challenges for both patients and physicians.
A large percentage of patients with chronic pain disorders have preexisting comorbid addiction disorders or such disorders develop after receiving treatment for pain. Studies have found rates as high as 15% to 28% for current substance disorders and 2% to 54% for lifetime prevalence in chronic pain patients, both rates significantly higher than in the general population. In one study of 200 patients with low back pain it was found that substance use and anxiety disorders seem to precede the onset of chronic pain. In the primary care setting it has been shown that substance use disorders precede the onset of chronic pain in 77% of patients who are actively using illicit substances and in 63% of patients with lifetime substance use disorders. Even though a significant proportion of patients seeking treatment of their pain may have a comorbid addiction problem, addiction problems can make it difficult to diagnose and treat pain. Chronic pain is more likely to develop in those with a preexisting history of substance abuse, and comorbid substance use disorders are more likely to develop in those with chronic pain and no history of substance abuse than in those without pain. It behooves the pain physician to have a good understanding of how pain and addiction are intertwined to skillfully manage these problems in an attempt to prevent worse outcomes.
Patients with chronic pain often have other psychiatric comorbid conditions (such as major depression or a generalized anxiety disorder), which may increase the risk for substance abuse and thereby create a more complex diagnostic and treatment conundrum for treating these patients’ pain. Some data suggest connections between chronic pain, mood disorders, and substance abuse. Moreover, it has been shown that patients who have chronic pain are not only at a higher risk for opioid abuse but also have higher rates of mood disorders. This constellation of diagnoses and problems compounds the difficulty that a physician will face when attempting to treat pain in patients who fall into this category.
This chapter covers the scope of these issues, from the neurobiology of addiction, to characterizing those at risk for opioid misuse and distinguishing opioid misuse without major negative consequences from prescription opioid addiction, to treatment considerations in patients with pain and substance use comorbidity. The topics are discussed primarily from the perspective of treatment of non–cancer-related pain with opioids. Even though those with cancer-associated pain are also at risk for substance use disorders, this phenomenon has not been well described.
Neurobiology of Addiction to Opioids
Any drug addiction is now understood to be a disease that is very much brain based. This phenomenon is a consequence of repeated exposure to the addictive drugs that leads to behavior characterized by loss of control over the use of such drugs. The behavioral abnormalities are connected to physiologic underpinnings, which mutually reinforce each other, and substance use disorders can be thought of as disorders of motivated behavior. Effective treatment involves simultaneously changing behavior and addressing the underlying physiologic drives sustaining the aberrant behavior. Addiction can be conceptualized as a chronic neurobiologic disease and a model of the relationship between the brain and behavior.
There remains a great deal of uncertainty regarding the exact neural correlates of addiction. Nonetheless, it is believed that key brain regions constituting the brain networks for addiction are found within the mesocorticolimbic dopamine systems, which start in the ventral tegmental area and connect to the amygdala, prefrontal cortex, and nucleus accumbens ( Fig. 51.1 ).
This pathway has been called the “dopamine reward pathway,” and all addictive drugs ultimately act through different mechanisms to potentiate euphoria or other positive reward symptoms that subsequently reinforce behavior for ongoing use of the drug. Opioids, in particular, work by inducing the release of dopamine in the ventral tegmental area and by binding to receptors in the nucleus accumbens. It has been postulated that the experience of withdrawal uses this same pathway to create the negative reinforcement that contributes to compulsive behavior and cravings.
Moreover, some of the biologic correlates connecting negative affect, increased pain, and opioid use have been described. These include the spinolimbic pathway, also known as the “medial pain system.” This pathway travels parallel to the spinothalamic tracts in the spinal cord and receives direct input from the dorsal horn of the spinal cord. This pathway will lead to regions in the brain, such as the anterior cingulate cortex, insula, and prefrontal cortex, that not only process both pain and affect but are also regions with a very high concentration of opioid receptors.
Vulnerability to the development of addiction is very much linked to genetic factors, as shown by genetic epidemiologic studies using twin, family, and adoption designs. Heritability can range from 0.3 to 0.5, depending on the drug of use. Although a specific “addiction gene” has not been identified, these studies point to a very strong biologic influence of addiction, whose assessment must be incorporated into the everyday clinical practice of addiction medicine and pain medicine. Thus, taking a detailed family history, including a family history of substance abuse, is valuable in providing data for comprehensive pain assessment. The different terminology used in the context of chronic pain with addiction and opioid misuse or abuse is summarized in Box 51.1 .
Pain is an unpleasant sensory and emotional experience associated with actual or potential tissue damage or described in terms of such damage.
Addiction is a chronic, relapsing brain disease characterized by compulsive drug behavior and use despite harmful consequences.
Pseudo-addiction is a condition in which patients taking opioids seek additional opioid medications because of inadequate dosing. These patients may exhibit behavior suggestive of addiction, but it resolves with an increase in opioid dose to provide adequate analgesia.
Iatrogenic addiction is a condition in which patients without a genetic predisposition for abuse are overly prescribed opioids, thereby leading to addiction.
Physical dependence is a state of adaptation that causes a drug class–specific withdrawal syndrome because of abrupt drug cessation, rapid reduction, or use of an antagonist.
Tolerance is an adaptation state that develops over time to a drug that requires increased doses to create the same drug effect or a reduction in one or more of a drug’s effect over time.
Misuse is the use of medications other than as directed whether willfully or unintentionally and regardless of whether harm results.
Abuse is the use of illicit or licit substances intentionally for nonmedical purposes.
Diversion is the intentional removal of a drug from legitimate distribution and dispensing channels. Much of the opioid medications “sold on the street” have come from pharmacies.
Aberrant behavior is a breach of mutually established medical boundaries by the patient.
Nosology of Prescription Opioid Misuse, Abuse, and Addiction
Many terms are used to describe substance use disorders in patients with chronic non–cancer-related pain, and clarification of the terminology is important. The American Academy of Pain Medicine (AAPM), the American Pain Society, and the American Society of Addiction Medicine (ASAM) define prescription opioid addiction in patients with pain as “a primary, chronic, neurobiologic disease that is characterized by behaviors that include one or more of the following: impaired control over drug use, compulsive use, continued use despite harm, and craving.” As noted, the behavioral characteristics of prescription opioid addiction may be perpetuated by a physiologic drive that comes with using prescription opioids ; in this case the mesolimbic motivational circuits are “hijacked” to perpetuate a disorder of motivated behavior.
For many pain medicine and addiction specialists, this definition of addiction is preferred in patients prescribed opioids for pain over the Diagnostic and Statistical Manual of Mental Disorders , Fourth Edition (DSM-IV), definition of substance dependence because physical dependence in these patients, as evidenced by tolerance and withdrawal, is normal. Although the DSM-IV definition does not require tolerance or withdrawal to make the diagnosis of substance dependence, these conditions do fulfill two of three major criteria required to make the diagnosis ( Table 51.1 ). Thus, there are phenomenologic quandaries in applying the DSM-IV criteria for evaluation of substance dependence in patients prescribed opioids for pain. Given these issues, the AAPM and ASAM refer to substance misuse in this patient group as the use of any drug in a manner other than how it is indicated or prescribed. Substance abuse is defined as the use of any substance when such use is unlawful or detrimental to the user or others.
Brief Symptom Descriptor | Abstracted DSM-IV Definition |
---|---|
Abuse Symptoms | |
Role impairment | Frequent intoxication leading to failure to fulfill major role obligations |
Hazardous use | Recurrent use when it is physically hazardous (e.g., drunk driving) |
Legal problems | Recurrent substance-related legal problems |
Social problems | Continued use despite social or interpersonal problems caused or exacerbated by use |
Dependence Symptoms | |
Tolerance | Need to consume more to achieve the same effect; decreased effect with the same amount |
Withdrawal | Signs of withdrawal syndrome; use to avoid withdrawal |
Larger/longer | Often using more or for a longer period than intended |
Quit/cut down | Persistent desire or unsuccessful attempts to quit or cut down substance use |
Much time spent using | Lots of time spent using, obtaining, or being affected by a substance |
Reduced activities | Important social activities given up or reduced because of substance use |
Psychological/physical causes | Continued use despite psychological or physical problems or problems exacerbated by use |
Hence, opioid misuse may indicate a treatment compliance issue or may signal a more serious addiction problem if accompanied by a lack of control over use despite negative consequences. These distinctions are somewhat blurry, and in a clinical pain medicine practice it is often unclear whether a patient is simply noncompliant with the medication or is truly dependent. The presence of craving is central to this distinction in applying the AAPM and ASAM criteria for prescription opioid addiction. Moreover, DSM-V will add craving to the diagnostic criteria for opioid addiction and is changing the terminology from opioid dependence to opioid addiction . However, it remains unclear to what extent craving is indicative of prescription opioid dependence or addiction since those without opioid dependence who are taking prescription opioids have appropriately also reported some craving. Furthermore, across many different substances, reporting craving is significantly associated with a substance use disorder. A few studies have examined craving in patients with pain who have been prescribed opioids, and craving is significantly associated with an elevated risk for opioid misuse.
Nosology of Prescription Opioid Misuse, Abuse, and Addiction
Many terms are used to describe substance use disorders in patients with chronic non–cancer-related pain, and clarification of the terminology is important. The American Academy of Pain Medicine (AAPM), the American Pain Society, and the American Society of Addiction Medicine (ASAM) define prescription opioid addiction in patients with pain as “a primary, chronic, neurobiologic disease that is characterized by behaviors that include one or more of the following: impaired control over drug use, compulsive use, continued use despite harm, and craving.” As noted, the behavioral characteristics of prescription opioid addiction may be perpetuated by a physiologic drive that comes with using prescription opioids ; in this case the mesolimbic motivational circuits are “hijacked” to perpetuate a disorder of motivated behavior.
For many pain medicine and addiction specialists, this definition of addiction is preferred in patients prescribed opioids for pain over the Diagnostic and Statistical Manual of Mental Disorders , Fourth Edition (DSM-IV), definition of substance dependence because physical dependence in these patients, as evidenced by tolerance and withdrawal, is normal. Although the DSM-IV definition does not require tolerance or withdrawal to make the diagnosis of substance dependence, these conditions do fulfill two of three major criteria required to make the diagnosis ( Table 51.1 ). Thus, there are phenomenologic quandaries in applying the DSM-IV criteria for evaluation of substance dependence in patients prescribed opioids for pain. Given these issues, the AAPM and ASAM refer to substance misuse in this patient group as the use of any drug in a manner other than how it is indicated or prescribed. Substance abuse is defined as the use of any substance when such use is unlawful or detrimental to the user or others.
Brief Symptom Descriptor | Abstracted DSM-IV Definition |
---|---|
Abuse Symptoms | |
Role impairment | Frequent intoxication leading to failure to fulfill major role obligations |
Hazardous use | Recurrent use when it is physically hazardous (e.g., drunk driving) |
Legal problems | Recurrent substance-related legal problems |
Social problems | Continued use despite social or interpersonal problems caused or exacerbated by use |
Dependence Symptoms | |
Tolerance | Need to consume more to achieve the same effect; decreased effect with the same amount |
Withdrawal | Signs of withdrawal syndrome; use to avoid withdrawal |
Larger/longer | Often using more or for a longer period than intended |
Quit/cut down | Persistent desire or unsuccessful attempts to quit or cut down substance use |
Much time spent using | Lots of time spent using, obtaining, or being affected by a substance |
Reduced activities | Important social activities given up or reduced because of substance use |
Psychological/physical causes | Continued use despite psychological or physical problems or problems exacerbated by use |
Hence, opioid misuse may indicate a treatment compliance issue or may signal a more serious addiction problem if accompanied by a lack of control over use despite negative consequences. These distinctions are somewhat blurry, and in a clinical pain medicine practice it is often unclear whether a patient is simply noncompliant with the medication or is truly dependent. The presence of craving is central to this distinction in applying the AAPM and ASAM criteria for prescription opioid addiction. Moreover, DSM-V will add craving to the diagnostic criteria for opioid addiction and is changing the terminology from opioid dependence to opioid addiction . However, it remains unclear to what extent craving is indicative of prescription opioid dependence or addiction since those without opioid dependence who are taking prescription opioids have appropriately also reported some craving. Furthermore, across many different substances, reporting craving is significantly associated with a substance use disorder. A few studies have examined craving in patients with pain who have been prescribed opioids, and craving is significantly associated with an elevated risk for opioid misuse.
Signs of Problematic Opioid Use
One major concern for the long-term use of opioids in patients with chronic non–cancer-related pain is their potential for misuse and abuse. Multiple cross-sectional studies in clinic populations have indicated that treatment of noncancer pain with opioids is associated with a 40% prevalence of opioid misuse. Clinicians have reported several types of aberrant drug-related behavior (ADRB) that may be indicative of opioid misuse. Although such behavior is problematic and indicative of nonadherence to opioid therapy at the very least, many have not been empirically tested to distinguish opioid misuse without negative consequences from prescription opioid addiction. Of course, certain types of extreme behaviors, such as injecting oral formulations or compulsive, uncontrolled use of medication, have face validity suggestive of addiction. According to Portenoy, there are three major types of ADRBs: loss of control over the drug, compulsive drug use, and continued use despite harm. He suggested the following sets of drug-related behavior that may cause suspicion about problematic use in opioid-treated pain patients:
ADRB more predictive of addiction
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Prescription forgery
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Stealing or “borrowing” drugs from others
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Injecting oral formulations
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Obtaining prescription drugs from nonmedical sources
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Concurrent abuse of alcohol or illicit drugs
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Multiple dose escalation or other noncompliance with therapy despite warnings
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Multiple episodes of prescription “loss”
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Repeatedly seeking prescriptions from other clinicians or from emergency departments (EDs) without informing the prescriber or after a warning to desist
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Evidence of deterioration in the ability to function at work, in the family, or socially that appears to be related to use of the drug
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Repeated resistance to changes in therapy despite clear evidence of adverse physical or psychological effects from the drug
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Selling prescription drugs (which is termed diversion and is not indicative of a substance use disorder per se but does signify a major ADRB)
ADRB less predictive of addiction (may be more indicative of poorly controlled pain or misuse without significant negative consequences)
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Aggressive complaining about the need for more drug
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Drug hoarding during periods of reduced symptoms
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Requesting specific drugs
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Openly acquiring similar drugs from other medical sources
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Unsanctioned dose escalation or other noncompliance with therapy on one or two occasions
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Unapproved use of the drug to treat another symptom
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Reporting psychic effects not intended by the clinician
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Resistance to change in therapy associated with “tolerable” adverse effects with expressions of anxiety related to the return of severe symptoms
Savage in 2002 also formulated a short list of patterns that may suggest addiction (“look for the four C’s”):
Adverse C onsequences/harm as a result of use
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Intoxicated, somnolent, sedated
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Declining activity
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Irritable, anxious, labile mood
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Increasing sleep disturbances
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Increasing pain complaints
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Increasing relationship dysfunction
Impaired C ontrol over use/ C ompulsive use
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Reports lost or stolen prescriptions or medication
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Frequent early renewal requests
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Urgent calls or unscheduled visits
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Abusing other drugs or alcohol
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Cannot produce medication on request
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Withdrawal noted at clinic visits
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Observers reporting overuse or sporadic use
Preoccupation with use because of C raving
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Frequently missed appointment unless opioid renewal expected
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Does not try nonopioid treatments
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Cannot tolerate most medications
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Requests medication with high reward
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No relief with anything else except opioids
It is important to remember that many of the types of behaviors listed may occur occasionally in isolation in patients using opioids appropriately, for the most part in the treatment of their chronic pain. However, a pattern of such behavior in the context of titrated pain therapy may suggest the need for further evaluation to determine the presence of prescription opioid addiction. It is still unclear exactly which constellations of symptoms or behaviors accurately distinguish misuse from abuse and addiction. These are thought to exist on a continuum, with the most severe form of nonadherence—addiction—characterized by the four “C’s.”
Early and proper identification, as well as careful monitoring for signs of problematic opioid use and ADRB, is warranted. Once identified, several measures may be taken by the prescribing physician to control for such aberrant behavior and reduce risk for the subsequent development of an addiction problem, including the following:
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Writing an opioid pain treatment agreement, if one is not available, in which expectations and conditions for termination of opioid prescription are clearly outlined
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Increasing the number of office visits and more frequent monitoring
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Decreasing the number of medication dispensed per visit
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Performing random pill counts on visits
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Recommending the use of only one pharmacy
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Using prescription drug–monitoring programs (PDMPs) to determine whether the patient has been getting prescriptions from multiple providers, EDs, or both
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Avoiding early prescriptions and excluding any replacement of lost or stolen prescriptions
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Requiring police reports for stolen medications
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Performing random urine drug screens and considering consultation with an addiction specialist if true addiction to the opioid medication is suspected
Careful assessment is essential to determine the underlying cause and co-occurring physical and mental comorbid conditions that may contribute to such behavior. Reliance on patient self-reports of medication use to determine inappropriate behavior has been shown to be notoriously unreliable and inaccurate since patients tend to underestimate their medication use. Cook and colleagues found that when patients’ self-reports were compared with urine toxicology screens, the actual prevalence rate of drug use was approximately 50% higher than the estimate produced by self-reports. Berndt and coauthors also reported that 32% of patients’ self-reports of their use of medication did not match with their urine tests.
In addition, “gut feelings” by some prescribers who are confident that they can identify vulnerable individuals should be avoided since empirical evidence has shown them to be ineffective. Wasan and associates found that even though prescribers had judged only 14% of their chronic pain patients to have ADRB, approximately 50% were found to have positive urine drug screens for illicit drugs and 8.7% had no evidence of any opioids in their urine.
In an attempt to decrease the risk for opioid misuse and iatrogenic addiction to prescribed opioid medications, Gourlay and coworkers recommended establishing a policy of “universal precautions” when prescribing opioid analgesics:
- 1.
Making a diagnosis with appropriate differential
- 2.
Psychological assessment, including risk for addictive disorders
- 3.
Informed consent
- 4.
Treatment agreement (previously called an “opioid contract”)
- 5.
Preintervention and postintervention assessment of pain level and function
- 6.
Appropriate trial of opioid therapy with or without adjunctive medication
- 7.
Reassessment of pain score and level of function
- 8.
Regular assessment of the “four A’s” of pain medicine (analgesia, activity, adverse effects, and aberrant behavior)
- 9.
Periodic review of the pain diagnosis and comorbid conditions
- 10.
Proper documentation
Screening/Risk Tools for Substance Abuse
Screening for risk for addiction should be performed before chronic opioid therapy is initiated to provide the treating physician with clues about the necessity for increased monitoring in susceptible individuals and to assist in making the decision of whether to prescribe opioids at all. If opioid treatment results in good pain control, a better level of functioning, and improved overall quality of life, opioid treatment could reasonably be continued even in patients susceptible to addiction. However, the important point is that patients thought to be at greater risk for opioid misuse will require special attention with a focus on compliance and with proper communication about the potential risks and consequences if opioid treatment is getting out of control.
The ideal screening tool for medication misuse or abuse in patients with chronic pain should be easy to administer, reliable, and well validated. An outline of such different screening tools is summarized in Box 51.2 .
Well Validated Tools
Pain Medicine Questionnaire: high validity and reliability; patients answering the questionnaire may not feel opposed to or prejudiced against the questions since opioids are not specifically mentioned.
Current Opioid Misuse Measure (COMM): can identify aberrant drug-related behavior in patients who are currently taking opioids.
Screener and Opioid Assessment for Patients with Pain—Revised (SOAPP-R): consists of 24 items and a cut-off score of 14 or higher for classifying those at greater risk for opioid misuse.
Less Validated Tools
CAGE questionnaire (CAGE-AID): primarily used for brief screening for alcohol abuse but has been adapted to include drugs.
Short Michigan Alcoholism Screening Test (SMAST-AID): also adapted to include drugs.
Prescription Opioid Abuse Checklist: based on DSM-III-R parameters.
Prescription Drug Use Questionnaire (PDUQ): developed by Miotto and colleagues and includes 42 items to be administered by trained clinicians.
Substance Use Questionnaire: capable of differentiating between chronic pain patients and heroin street abusers.
Opioid Risk Tool (ORT): categorizes patients into low (score of 3 or lower), moderate (score of 4 to 7), or high (score of 8 or higher) risk for aberrant drug-related behavior.
Screening Tool for Addiction Risk (STAR) questionnaire: developed by specialists in both pain and addiction medicine. History of treatment in a drug or alcohol rehabilitation facility is a significant predictor of ongoing addiction with a positive predictive value of 93% and a negative predictive value of 5.9%.
DSM-III-R, Diagnostic and Statistical Manual of Mental Disorders , Third Edition, Revised.
Though conceptually distinct from instruments designed to detect existing addictive disorders, measures whose purpose is to predict aberrant prescription opioid–related behavior in pain patients are closely related, with identification of similar risk factors. As a whole, this body of research is remarkably consistent in identifying the most significant risk factors for predicting prescription opioid misuse: current reports of misuse, past or current history of an addiction disorder to any substance (except perhaps for alcohol dependence in remission for several years), concurrent negative affective disorder (such as major depression or an anxiety disorder), previous or current history of sexual or physical abuse, family history of substance use disorders, and a history of illegal activities. Remarkably, ongoing pain levels have not been shown to be strong, consistent predictors of opioid misuse, albeit some misuse behavior may purely be a consequence of underdosing of opioids (pseudo-addiction).
Urine Toxicology Screening
Urine toxicology screens continue to be the most widely used and possibly the “gold standard” for detecting illicit substance use in chronic pain patients treated with opioids. Patients should be screened at baseline before starting opioids and then periodically throughout the course of treatment. However, the results of baseline screening should be interpreted with caution and not considered indicative of future aberrant behavior. Katz and Fanciullo found that 72% of patients with positive baseline screens (i.e., inappropriate results) did not have evidence of any aberrant behavior after initiation of treatment. Conversely, patients with an initial negative toxicology screen may later demonstrate behavior indicative of problematic drug use. Many types of urine toxicology screens and many testing technologies are available, so it is important to choose the type of screening that most closely and accurately identifies the substances of interest.
Opioid Therapy Agreements
As noted, it is important for clinicians to discuss their management plan regarding chronic opioid therapy with their patients before initiating treatment and on an ongoing basis during therapy. The management plan should include the goals of therapy, how opioids will be prescribed and taken, alternatives to opioid therapy, expectations for follow-up, monitoring, and use of concomitant therapies, as well as potential reasons for terminating opioid therapy, which may include failure to meet the therapeutic goals, serious side effects, or repeated ADRB.
Although evidence of the most effective methods to convey this management plan is lacking, written documentation through an opioid therapy agreement signed by both the patient and clinician may be an appealing tool for managing many of the potential difficulties related to chronic non–cancer-related opioid therapy. Despite the widespread use of therapy agreements and some evidence of their effectiveness, their efficacy has not yet been proved (i.e., compared with a control condition in a prospective study). Nevertheless, multiple opioid therapy treatment guidelines appropriately emphasize the benefits of such an agreement in all patients prescribed opioids for noncancer pain. They can be particularly helpful for patients at higher risk for opioid misuse, to reinforce expectations about the appropriate and safe use of opioids, and to convey the consequences of violating such terms. The contents of signed opioid agreements may vary, and there is still insufficient evidence to guide specific recommendations on which provisions to include. Some common provisions include
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Obtaining opioids from one prescriber
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Filling opioid prescriptions at one designated pharmacy
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Random urine drug screens
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Office visits at a specified minimum interval
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Use of pill counts
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Limited prescriptions (in weekly or biweekly instead of monthly amounts)
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Description of behavior that may lead to discontinuation of chronic opioid therapy
Although the opioid agreement may be helpful in some ways, it may not be entirely benign for either the patient or clinician. There is always the potential of carrying some degree of stigma or even the appearance of punishment with such agreement forms, particularly in those with a history of addiction. It may also inappropriately reassure clinicians that patients are completely adherent to the treatment plan, which then results in less stringent monitoring of opioid use and treatment efficacy. Opioid agreements are still considered binding contracts and thus carry with them an increased risk for liability should the clinician violate their terms or place patients at risk for reduced autonomy. Careful consideration should be given to restrictions placed on patients, such as limitations on driving or prohibiting pregnancy, since the literature is still inconclusive on these subjects.
Prescription Drug–Monitoring Programs
PDMPs are statewide electronic databases that collect data on controlled substances dispensed in the state. They are housed by specified statewide regulatory, administrative, or law enforcement agencies (most commonly state boards of pharmacy). Information is stored in a central database and can be accessed by authorized users, including prescribers, dispensers, law enforcement for drug investigations, licensing and regulatory boards, Medicaid programs, medical examiners, and research organizations. Their main goal is to identify and prevent drug abuse and diversion, as well as to facilitate the identification of, intervention in, and treatment of persons addicted to prescription drugs. The data collected can help provide information for public health initiatives about the use and abuse trends of different substances statewide, including prescription opioids. PDMPs also ensure patient privacy since law enforcement personnel cannot access patient-specific PDMP data unless an active investigation is ongoing and health care providers can access only the PDMP data relevant to their patients.
Several studies have shown that PDMPs are effective when fully used. A 2010 study found that when PDMP data were used in an ED, 41% of cases had altered prescribing after the clinician reviewed PDMP data: 61% of the patients received no or fewer opioid pain medications than had been originally planned by the physician before reviewing the PDMP data, and 39% received more opioid medication than previously planned because the physician was able to confirm that the patient did not have a recent history of controlled substance use. Another 2010 independent evaluation of Kentucky’s PDMP, KASPER, found that 90% of those surveyed believed that KASPER was effective in preventing drug abuse, diversion, and doctor shopping.