Drugs of misuse act at local cellular and membrane sites that are within a neurochemical system that is called the reward and withdrawal pathway (
Fig. 59.1).
28 This pathway is in the mesolimbic dopamine system, and it involves, among other structures, the ventral tegmental area, nucleus accumbens,
amygdala, and prefrontal cortex of the primitive brain. Addiction is a neurobiologic disease that causes disruption of these pathways. This disruption is mediated via receptor sites and neurotransmitters. Central to this reward and withdrawal pathway is the neurotransmitter dopamine, which has been shown to be relevant not only to drug reward but also to food, drink, sex, and social reward.
29,30 Disruption of this neurochemical pathway by drugs of abuse may lead to addiction. Drug withdrawal can intensify with repeated drug use and can persist during prolonged periods of drug abstinence, a symptom complex known as the protracted abstinence syndrome.
31 This sensitization of a neural process related to drug cravings or to environmental stimuli such as sights, smells, and sounds associated with drugs (referred to as cues) leads to the progressive increase in drug-seeking behavior that characterizes addiction. Such sensitization appears to increase the attractiveness of the drug taking and that of the drug-associated stimuli.
32
The health care professional must recognize addiction as a treatable brain disease
33,34; that is, a distinct medical condition that may or may not be associated with the patient’s pain syndrome. However, when these do coexist, the successful treatment of either will require addressing both problems. In fact, as a general principle, all pain doctors should be talented amateurs in the context of identifying and treating substance use disorders (D. L. Gourlay, personal communication, verbal, July 2017).
Opioids can cause physical dependence and, upon abrupt discontinuation, withdrawal as a result of upregulation of the cyclic adenosine monophosphate (cAMP) pathway at the locus coeruleus.
31 This is a normal physiologic response to this class of medications. It should be noted that most of the medications capable of producing physical dependence are not associated with the disease of addiction.
Tolerance is also a natural, expected physiologic response that can occur with exposure to certain classes of drugs, especially alcohol and opioids. The
key to this definition is that all other factors remain stable so that just the physiologic response to the drug can be evaluated.
17 In fact, tolerance is neither good nor bad. It occurs at different rates, to different effects in different people, over time. So, although there is relatively rapid tolerance development to the cognitive blunting effects of the opioid class of drug, tolerance to the constipating effects of opioids rarely occurs. Unappreciated disease progress that is associated with dose escalation is termed
pseudotolerance,
35 a term that was coined to describe the apparent loss of analgesic effect in cancer patients with unrecognized increases in tumor burden.
35 Pharmacodynamic tolerance involves adaptations that occur at both the site of the drug action (e.g., receptor, ion channel, as well as in related systems more distal to it). For example, pharmacodynamic tolerance to opioids is evident at both the level of the opioid receptor in the locus coeruleus (primary) and in the dopaminergic reward pathways afferent to the site of this discrete drug action (secondary).
32 Persons addicted to heroin and chronic pain patients taking opioids can both exhibit tolerance to the drug.
BINARY CONCEPT OF PAIN AND ADDICTION
In the past, the literature has suggested that pain conditions and addictive disorders might be dichotomous phenomena.
11,14, 36 It has been said that in the context of a “legitimate” pain diagnosis, which usually meant a condition that made sense to the assessing health care professional, the likelihood of there being an addictive disorder was so small as to not even merit investigation. Unfortunately, if the patient had an obvious substance use disorder, very real and treatable pain conditions were often ignored. With time, this thinking was tempered somewhat to suggest that in the absence of a current or past personal or family history of a substance use disorder, the risk of addiction was very low indeed.
14 This dichotomous approach to pain and addiction has not served patients, health care professionals, or society well.
In reality, there is nothing about a genuine pain condition that is protective against having a concurrent substance use disorder
3; however, untreated pain, as a stressor, should always be considered in the assessment of relapse risk.
28 Although there are some data in the animal literature to suggest that acute pain may blunt the euphoric reward of some drugs including opioids,
37,38 this concept has largely been discounted. Patients with a substance use disorder are often disproportionate consumers of health care resources, especially in the context of trauma.
39,40 The presence of a preexisting substance use
disorder is not mitigated by a concurrent pain problem; it is complicated by it.
Although there is no evidence in the literature to suggest that those patients without past histories or apparent increased risk of substance use disorders become addicted as a result of rational pharmacotherapy for the treatment of any medical condition, including chronic pain, there is little credible evidence to the contrary either. Perhaps more relevant questions to ask are whether rational pharmacotherapeutic management of acute or chronic pain can reactivate a previously dormant substance use disorder or express an as yet unidentified genetic predisposition
3 toward substance misuse or addiction. In the authors’ opinion, the answer to both questions very likely is “Yes.”
11
Risk, of course, varies with circumstance. For example, the prevalence of alcoholism in the hospitalized general medical population is estimated at 19% to 26%,
41 whereas in the trauma subset, the prevalence rises to 40% to 62%.
40 Regardless of what the actual risk is, it is clear that no one specific marker can reliably identify the at-risk pain patient, so careful boundary setting for all patients is strongly recommended.
14 However, boundary setting is not without potential risk. It is interesting to note that in some cases, aberrant behavior on the part of the patients may be driven, if not created by overly proscriptive rules and demands placed on them by their treatment provider/team.
Take, for example, the patient that is forced to provide urine drug samples on a twice-weekly basis. It might be considered “aberrant” if the patient appears unwilling to comply. In fact, many would consider even weekly urine drug testing (UDT) onerous and so the disruption in the patients’ life might well be considered unacceptable. If boundaries and limits are set excessively tight, even “normal” patients will be forced to step out of bounds. Not only is this excessive, but there is no evidence in the literature to suggest this pattern of testing is either clinically useful or medically necessary.
42
Not all aberrant behavior reflects drug misuse or addiction. Some individuals who do not meet the diagnostic criteria for addiction may also use medications and other drugs problematically. This group is sometimes referred to as “chemical copers.”
43 These individuals lack the skills commonly acquired during childhood and adolescence and tend to turn to external sources for support in dealing with life’s problems. Often, however, these patients suffer from complex, multidimensional problems that may only be partially responsive to even optimum pharmacotherapy in the absence of a biopsychosocial treatment plan. Unidimensional problems may respond to unidimensional pharmacologic solutions. Multidimensional problems however may transiently respond to pharmacologic interventions but rarely in a sustainable fashion.
11
It is only by aggressive investigation and rational pharmacotherapeutic management of the pain that this diagnosis can be made.
The diagnosis of addiction is often made prospectively over time.
11 When the patient’s behavior remains aberrant despite the appropriate management of the underlying painful condition with reasonably set limits, substance misuse or addiction should be considered. In contrast,
the diagnosis of pseudoaddiction is made retrospectively,
11 meaning that with appropriate management of pain, aberrant behavior is reduced or eliminated.
11,14 Boundary setting may include interval dispensing and contingency prescribing. Interval dispensing requires the patient to see other members of the health care team, such as a staff member of the prescriber or the pharmacist, on a more frequent basis than the actual prescriber. Thus, interval dispensing can be a simple and effective means to help patients keep from “borrowing (medications) from tomorrow to pay for today,” thereby reducing the risk of running out of medications early. With contingency prescribing, receiving the next prescription is contingent on something such as bringing bottles in for “pill counts” or mandatory attendance at all appointments.
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