Universal precautions to reduce stimulant misuse in treating adult ADHD
ABSTRACTIn the United States, stimulants remain the approved pharmacotherapy of choice for adults with attention-deficit/hyperactivity disorder (ADHD). Many patients respond to these drugs, but stimulants also have a significant potential for misuse. This article suggests the “universal precautions” approach to reducing these risks while promoting appropriate medication use.
KEY POINTS
- Untreated adult ADHD is associated with negative outcomes that include unemployment, arrests, divorce, and psychiatric comorbidities.
- Available ADHD guidelines suggest that children and adults who respond to pharmacotherapy should continue it for as long as it remains effective. In this context, there is increasing recognition of adult ADHD as a valid and treatable disorder.
- Following the guidelines of universal precautions in the diagnosis and treatment of adult ADHD can alleviate clinicians’ concerns when diagnosing and treating this disorder.
HOW SHOULD THESE RISK FACTORS AFFECT TREATMENT?
Although no formal scoring system exists to help clinicians risk-stratify these patients, the presence of multiple risk factors suggests the need for vigilance.14 Physicians should prescribe agents with less potential for abuse and monitor these patients more intensely.
Short-acting stimulant medications are the most likely to be abused, as phasic dopamine increase is more reinforcing than therapeutic dopamine release.24 Longer-acting stimulant medications are less likely to be abused, and they provide better symptom relief, as tonic dopamine release maintains a steady state and increases the therapeutic efficacy of these medications.25 For example, methylphenidate extended-release tablets have an osmotic oral controlled-release system and are less likely to be crushed for recreational inhalation.6,14
Lisdexamfetamine is a prodrug therapeutically inert until converted to d-amphetamine when lysine is cleaved from the molecule. This medication may be a good option for patients at high risk of misuse because it is tamper-resistant. However, it still may be subject to misuse for performance enhancement.26,27
The nonstimulant atomoxetine is also approved for ADHD, has no abuse potential, and may be particularly useful when anxiety, mood, and substance use disorders co-occur with ADHD.6 Rarely, atomoxetine can damage the liver, and liver function tests should be monitored if right upper quadrant pain develops.4,10
Other nonapproved agents such as bupropion and desipramine also have been used empirically and off-label for ADHD.4,10
Overall, treatment should be selected according to the risk of misuse of stimulant medication and the patient’s comorbidities.
INFORMED CONSENT
Informed consent may help patients appreciate the risks and benefits of the treatment options and develop realistic expectations about treatment.26 Patients are instructed to take their stimulant medications as prescribed and are informed of the risks of combining stimulants with other substances, particularly those that may interact with stimulants (eg, cocaine) and raise the risk of seizures and cardiovascular complications.
Stimulant medications lead to elevations in blood pressure and heart rate, although large-scale studies have shown no increase in the rate of serious cardiovascular events when these drugs are used appropriately.6 Less serious side effects associated with stimulant medications include insomnia, weight loss, decreased appetite, dry mouth, headache, and rarely, depression and anxiety.6
Patients need to be warned about diversion and abuse liability of stimulant medications, as well as alternative treatments.
The nonstimulant atomoxetine has no reinforcing properties but also raises the blood pressure and heart rate.6 As with stimulants, these elevations are generally minimal, time-limited, and of minor clinical significance.4,10 Frequent reasons to prescribe atomoxetine include poor tolerability of stimulants and a history of substance abuse. In addition, women with ADHD and high levels of emotional dysregulation or social anxiety appear to be particularly responsive to atomoxetine.6
Another consideration is cognitive behavioral therapy, which can augment the effects of pharmacotherapy.4 Cognitive behavioral therapy focuses on time management, prioritization, organization, problem-solving, motivation, and emotional regulation.4
Finally, patients also need to understand the possible consequences of nontreatment.5 Adults with untreated ADHD have high rates of academic and occupational difficulties, anti-social behaviors, and other forms of psychosocial adversity.4,5
Overall, this process should involve discussing risks and benefits of treatment options with the patient and promoting joint decision-making.
TREATMENT AGREEMENTS
Stimulant medications are classified by the US Drug Enforcement Administration as schedule II substances due to their abuse potential.20
It is important to inform patients of the addictive nature of the medication and to instruct them on how to store stimulants safely.27 Patients need to know that giving away or selling these medications is illegal.27
Treatment agreements establish rules for prescribing and are signed by the patient before initiating therapy.28,29 Patients are expected to attend all of their appointments, receive their prescriptions from one doctor, and obtain their medication from one pharmacy. These agreements may also require patients to submit to monitoring with random urine drug screens.29 Overall, they underscore the need for patients to follow a treatment plan in order to continue therapy with controlled substances.29
Manning27 recommends using agreements for high-risk college students prescribed stimulant medications. Red flags for misuse include signs of active substance use (eg, intoxication, a pattern of “lost” prescriptions, and doctor-shopping).27
The effectiveness in reducing risk of misuse in the adult ADHD population has not yet been investigated. Nonetheless, a method of communicating the seriousness of stimulant misuse to adult patients is essential to ADHD care.
STAYING ON TRACK
In the clinical setting, treatment response is measured not just by symptom reduction, but also by functional improvement. Thus, clinicians and patients must set functional goals whenever possible.27 Successful progress toward these goals justifies continuation of therapy, whereas lack of improvement signals the need to reconsider stimulant therapy.27
MONITORING AND DOCUMENTATION
Adults with ADHD present with varying levels of functional impairment and comorbidities, which may require different levels of monitoring.30 Not all patients with ADHD respond optimally to stimulant medications or tolerate them well.31,32 Hence, monitoring parameters for therapeutic change and adverse outcomes are important in that they guide the alteration or even discontinuation of pharmacotherapy.4,6,14
Documenting the decision-making process to continue stimulant medications under certain circumstances is also essential. Documentation should include discussion of goals and expectations, risks and benefits, and alternatives to stimulant use.
In adults, risk of stimulant medication misuse adds a new layer of complexity to monitoring.13,14 Adults may get multiple prescriptions from multiple providers, seek early refills, fill prescriptions at different pharmacies, or alter formulations. Many states track stimulant prescription use, and prescribers can use this information to determine if patients are refilling their prescriptions appropriately or obtaining stimulants from more than one provider.
Although these monitoring strategies are useful,6 it is prudent to structure the level of monitoring according to the patient’s risk of adverse events or medication misuse.14,27 Gourlay and Heit15 proposed the following “four-A” mnemonic for four domains to be explored at each visit in patients receiving pain medicine. This mnemonic can be applied to adult ADHD patients to more accurately monitor the patient throughout treatment.
THE ‘FOUR-A’ MNEMONIC
ADHD symptoms
Several ADHD scales can be used to track symptom changes over time.33 However, these self-report scales may be subject to positive illusory bias, a phenomenon observed in individuals with ADHD in which they tend to overrate their functioning,34 which may limit the accuracy of self-report scales.35
Activities of daily living
Since patients with ADHD tend to overrate their functioning in various aspects of living, collateral information should be gathered to corroborate patient self-reports whenever possible.
Adverse events
Blood pressure, heart rate, and weight should be assessed at baseline and monitored during stimulant treatment. Other symptoms to monitor include gastrointestinal distress, headache, aggression, depression, appetite, and sleeping habits.4,6 More intensive monitoring (eg, electrocardiography) may be indicated for those with hypertension and cardiovascular risk factors.
Aberrant behavior
Monitoring for misuse and diversion of stimulant medications is essential, as ADHD itself is a risk factor for addiction.20,21 Pill counts, prescription monitoring programs, urine drug screens, and collateral informants have all been proposed but not studied in monitoring for the misuse of stimulant medications.27 Before prescribing, it is prudent to check the prescription monitoring program, get a urine drug screen, and discuss any positive findings with the patient.36,37
Treatment agreements ensure that patients are aware of the consequences of misuse and allow the clinician to reference prior discussion when terminating treatment with stimulants.
LIVES CAN BE ENHANCED
ADHD is a common disorder that arises in childhood and can persist throughout life. Adults with untreated ADHD are at risk of severe impairments in various domains of functioning. Stimulant medications are an effective treatment but may be diverted into the street market. Using the universal-precautions model may reduce the risks of both nontreatment of ADHD and misuse of stimulants.
Accordingly, clinicians need to confirm the ADHD diagnosis, assess comorbidities, estimate risk of misuse, and provide informed consent prior to prescribing. Subsequent monitoring should involve the use of treatment agreements and evaluating treatment response, paying particular attention to ADHD symptom control but also to level of function, adverse effects, and aberrant behavior.
With these principles in mind, clinicians can address the risks of misuse and potentially enhance the lives of people who may have been suffering substantially due to lack of appropriate care.