Pharmacological interventions for adolescents and adults with ADHD: stimulant and nonstimulant medications and misuse of prescription stimulants

Abstract

Attention-deficit/hyperactivity disorder (ADHD) is a neurodevelopmental disorder characterized by symptoms of inattention, hyperactivity, and impulsivity that cause functional impairment. Recent research indicates that symptoms persist into adulthood in the majority of cases, with prevalence estimates of approximately 5% in the school age population and 2.5%–4% in the adult population. Although students with ADHD are at greater risk for academic underachievement and psychosocial problems, increasing numbers of students with ADHD are graduating from high school and pursuing higher education. Stimulant medications are considered the first line of pharmacotherapy for individuals with ADHD, including college students. Although preliminary evidence indicates that prescription stimulants are safe and effective for college students with ADHD when used as prescribed, very few controlled studies have been conducted concerning the efficacy of prescription stimulants with college students. In addition, misuse of prescription stimulants has become a serious problem on college campuses across the US and has been recently documented in other countries as well. The purpose of the present systematic review was to investigate the efficacy of prescription stimulants for adolescents and young adults with ADHD and the nonmedical use and misuse of prescription stimulants. Results revealed that both prostimulant and stimulant medications, including lisdexamfetamine dimesylate, methylphenidate, amphetamines, and mixed-amphetamine salts, are effective at reducing ADHD symptoms in adolescents and adults with ADHD. Findings also suggest that individuals with ADHD may have higher rates of stimulant misuse than individuals without the disorder, and characteristics such as sex, race, use of illicit drugs, and academic performance are associated with misuse of stimulant medications. Results also indicate that individuals both with and without ADHD are more likely to misuse short-acting agents than long-acting agents. These findings have implications for intervention, prevention, and future research.

Keywords:

• ADHD symptomatology
• pharmacotherapy
• nonmedical stimulant use
• lisdexamfetamine
• methylphenidate
• amphetamine

Introduction

Attention-deficit/hyperactivity disorder (ADHD) is a neurodevelopmental disorder characterized by symptoms of inattention, hyperactivity, and impulsivity that cause functional impairment.¹ Previously, ADHD was believed to be primarily a disorder of childhood that would be outgrown with the onset of puberty. Recent research, however, indicates that symptoms persist into adulthood in the majority of cases, with prevalence estimates of approximately 5% in the school age population and 2.5%–4% in the adult population.^1–4 Academic problems are prevalent among children and adolescents with ADHD and are associated with inattention and difficulty remaining seated, following directions, and completing assignments.⁵ In addition, children and adolescents with ADHD often demonstrate disruptive, defiant, and hostile behavior.^6,7 Given these academic and behavioral difficulties, children and adolescents with ADHD are more likely than their non-ADHD peers to receive lower grades, fall behind academically, receive special education services, repeat grades, and drop out of high school and are less likely to pursue college.^5,8 Research suggests, however, that the symptoms of ADHD are often manifested differently in adolescence compared with in childhood. For example, symptoms of hyperactivity tend to decrease in adolescence relative to childhood and instead may be manifested as symptoms of cognitive or internal restlessness.^9–11 Adolescents with ADHD, however, continue to demonstrate similar levels of impairment as younger children with ADHD, including academic underachievement and difficulties with peers and social relationships, as well as various high-risk behaviors, including reckless driving and sexual behavior and substance use.¹²

Despite these impairments, students with ADHD are increasingly graduating from high school and attending college.¹³ However, information is lacking concerning the exact prevalence of ADHD among college students, due to privacy protection for students with disabilities under the Americans with Disabilities Act of 1990 and because many college students who meet diagnostic criteria for ADHD may not have been diagnosed with the disorder.^14,15 Therefore, more information is sorely needed regarding the prevalence of the disorder in the college population and its impact on student functioning. Several investigations have examined the prevalence of ADHD and the functioning of college students with ADHD symptomatology, most of which have relied on student self-report. For example, Weyandt et al¹⁶ conducted the first study assessing ADHD symptomatology among college students and found that approximately 2.5%–8.7% of participants reported significant ADHD symptoms, depending on the criteria employed. More recent estimates are similar to those of Weyandt et al, indicating that approximately 2%–10% of college students have significant ADHD symptoms and that approximately 50% of students who receive disability services do so because of ADHD.^15,17–19

In terms of the academic and psychosocial functioning of college students with ADHD, Norwalk et al²⁰ found that students with ADHD had greater difficulty with college adjustment and poorer study habits and study skills than students without the disorder. Similarly, Shaw-Zirt et al²¹ found that college students with ADHD, matched with non-ADHD peers on age, sex, and grade point average (GPA) (a measure of academic performance), reported poorer academic, social, and emotional adjustment than non-ADHD participants. Other studies have revealed that college students with ADHD tend to have lower GPAs, higher rates of academic probation, and poorer test-taking strategies and are less likely to graduate from college.^2,22–24 Self-reported psychological distress also appears to be more common among college students with ADHD than among those without the disorder, including poorer self-esteem and increased levels of depression and anxiety.^21,25–27 Collectively, these findings indicate that students with ADHD and elevated ADHD symptomatology are beset by various challenges in the college environment. To improve the outcomes of college students with ADHD, proper identification of the disorder is crucial so that effective prevention and intervention strategies may be developed and implemented.

Medical and nonmedical use of prescription stimulants

Pharmacotherapy is the primary treatment option for children, adolescents, and adults with ADHD, including college students.^28,29 US Food and Drug Administration (FDA)-approved medications for ADHD include 1) stimulants such as methylphenidate (MPH) (eg, Ritalin [Novartis International AG, Basel, Switzerland], Concerta [Janssen Pharmaceuticals Inc., Titusville, NJ, USA]), dextroamphetamine (D-AMP) (eg, Adderall [Shire plc, Dublin, Ireland], Dexedrine [GlaxoSmithKline plc, London, UK]), and lisdexamfetamine dimesylate (LDX) (eg, Vyvanse [Shire Inc., Wayne, PA, USA]), a prostimulant; and 2) nonstimulants (eg, atomoxetine, [Strattera; Eli Lilly and Company, Indianapolis, IN, USA]).

Nonstimulants (eg, atomoxetine) have been demonstrated to be safe and effective for improving ADHD symptoms among children, adolescents, and adults.^30–33 Nonstimulants have been found to be effective for individuals who do not respond to stimulants and have also been recommended for treating patients with ADHD who have comorbid substance use disorder (SUD). Nonstimulants, unlike stimulants, primarily affect the norepinephrine neurotransmitter system rather than the dopaminergic system and consequently have a lower potential for abuse than stimulant medications. Stimulant medications, however, remain the first line of pharmacotherapy for individuals with ADHD.^28,29,32 An extensive body of literature attests that stimulant medication, when used as prescribed, is safe and efficacious for improving attention and decreasing hyperactivity and impulsivity symptoms.^34–42 Although individuals with ADHD may greatly benefit from prescription stimulant medication, given their abuse potential when not taken as prescribed, prescription stimulants have been classified as schedule II medications by the FDA. A schedule II classification indicates that although the medication has been approved for medical use, it has a high potential for abuse, which, in turn, may lead to physiological and/or psychological dependence.⁴³

Numerous studies have documented that the nonmedical use of prescription stimulants, defined here as the use of stimulant medication in the absence of a valid prescription and use of prescription stimulants other than as prescribed, is a growing problem on college campuses, and college students typically report that stimulant medication is easy to obtain on campus.^44–52 Indeed, large numbers of students claim to have engaged in the nonmedical use of prescription stimulants, which is reflected in lifetime prevalence rates of prescription stimulant misuse ranging from 5% to nearly 34% of students.^53,54 Researchers have speculated that this increase may, in part, be explained by increasing numbers of college students receiving stimulant medication treatment for ADHD who may be distributing their medication to their peers, who may, in turn, misuse it.^44,49 Due to the significant health risks associated with the nonmedical use of prescription stimulants, this behavior poses a serious public health issue.⁵⁵ Consequently, studies have attempted to elucidate the characteristics of prescription stimulant misuse as well as risk and protective factors associated with this behavior.

The most commonly reported and the most strongly endorsed reason for taking prescription stimulants nonmedically is to improve attention and alertness while studying, taking exams, and writing papers: ie, cognitive and academic enhancement.^{44,45,49,52,53} Research has also identified several risk factors for stimulant misuse, including demographic variables such as sex, ethnicity, and psychological risk factors, such as depressive symptomatology and symptoms of inattention. The identification of malleable predictors such as the academic and psychosocial functioning of students is particularly important for prevention and intervention strategies for prescription stimulant misuse.^56–58

Purpose of the present study

Given the positive association between psychological factors, ADHD symptoms, and the nonmedical use of prescription stimulants, and that college students report misusing stimulants primarily to enhance their cognitive and academic functioning, it is highly plausible that, by doing so, students are trying to compensate for the struggles they encounter in the college environment. In fact, some researchers have hypothesized that college students may be using prescription stimulants nonmedically as a coping strategy to treat ADHD symptoms: ie, to “self-medicate”.^49,57 Although preliminary evidence indicates that prescription stimulants are safe and effective for college students with ADHD when used as prescribed, very few controlled studies have been conducted on the efficacy of prescription stimulants for college student functioning specifically.³⁷ The question that arises, then, is whether the medical use of prescription stimulants leads to reductions in symptoms and improved academic and psychosocial outcomes. Further, is the medical use of prescription stimulants associated with increased nonmedical use of these medications? What is the scope of prescription stimulant misuse among college students? Are certain types of medications associated with greater potential for misuse than others? Answers to these questions will greatly inform both the treatment of ADHD among college students and prevention and intervention efforts aimed at reducing the nonmedical use of prescription stimulants on college campuses.

The present study attempted to answer these questions by conducting a systematic review of the literature concerning studies that investigated 1) the efficacy of prescription stimulants for adolescents and adults, including college students, with ADHD and 2) the nonmedical use and misuse of prescription stimulants.

Methods

Search and retrieval

A systematic literature review was conducted according to Okoli and Schabram’s⁵⁹ eight-step guide. Accordingly, all researchers were trained in the protocol for searching and identifying relevant articles. Although the first study to identify stimulant misuse was conducted in 2000 by Babcock and Byrne,⁴⁶ a substantial number of studies addressing stimulant misuse appeared in 2002. Therefore, we attempted to identify and retrieve all empirical studies published after 2002 that examined the efficacy of stimulants and nonstimulants and stimulant misuse with adolescents and adults. The search and retrieval process included a comprehensive search of the following bibliographic databases: PsycINFO, PsycARTICLES^®, MEDLINE, and ScienceDirect. Keywords and eligibility criteria were established separately for each subject. In order to identify and retrieve empirical studies that examined the efficacy of stimulants among adolescents and adults, the following keywords were used: “efficacy” + “stimulants”, “efficacy” + “Ritalin”, “efficacy” + “Adderall”, “efficacy” + “Concerta”, “ADHD” + “Ritalin”, “ADHD” + “Adderall”, and “ADHD” + “Concerta”. Keywords used to identify research examining the efficacy of nonstimulants and prostimulants among adolescents and adults included the following: “efficacy” + “nonstimulants”, “efficacy” + “Strattera”, “efficacy” + “Vyvanse”, and “efficacy” + “prostimulant”. Finally, keywords used to identify research examining stimulant misuse among adolescents and adults were: “prescription stimulant” + “misuse”, “prescription stimulant” + “illicit”, “methylphenidate” + “misuse”, “methylphenidate” + “illicit”, “prescription stimulants” + “nonmedical”, and “methylphenidate” + “nonmedical”.

Eligibility criteria

Studies for all search subjects were selected for review based on the following criteria.

1. The study was published in English.

2. The study was published no earlier than 2002.

3. The study included a minimum sample size of 20 subjects.

4. The study used an original dataset (meta-analyses and reviews were excluded).

5. The study was relational, experimental, or quasiexperimental.

6. The study could be conducted worldwide.

7. The sample included adolescents (ie, participants with a mean age of ≥12 years) and/or adults. Note that studies including both children and adolescents were included if the mean age of participants was ≥12 years. Studies that did not report the participants’ mean age and included samples with a majority of participants aged <12 years were excluded.

8. The sample included human subjects only and included no special groups except for persons with ADHD and learning disabilities.

9. The study used only FDA-approved medication for ADHD.

10. Eligibility criteria were established specifically for research examining the efficacy of stimulants, prostimulants, and nonstimulants.

11. The sample included a control group (guanfacine studies were excluded, as well as studies examining efficacy of nicotinic agonists).

Results

The search process resulted in identifying 2,103 sources, of which 76 met eligibility criteria. Specifically, nine studies examined the efficacy of LDX, 14 explored the efficacy of MPH, three assessed the efficacy of amphetamine (AMPH), three explored the efficacy of both MPH and AMPH in adolescents and adults, and 47 examined stimulant misuse among adolescents and adults. Although included in the initial search process, no studies examining the efficacy of nonstimulants met eligibility criteria for the present review.

Efficacy of prostimulants for adolescents and adults

As seen in Table 1, all of the included studies (n=9) demonstrated a significant improvement in the measured outcomes from LDX compared with placebo. Six of the nine included studies reported effect sizes, all of which (based on Cohen’s estimates of small, medium, and large) reported medium to large LDX-related effects for improvement in ADHD and related symptoms.^{35,37,60–64} Although the majority of studies examined LDX effects among adults, only one study examined its efficacy among a sample of adolescents. Specifically, Findling et al⁶⁵ reported that at varying doses (30, 50, and 70 mg/day), LDX was more effective at treating ADHD than placebo. Regarding adults with ADHD, improvements from LDX have been reported for quality of life, performance productivity, and executive function.^35,64,66 Large effects from LDX on improved executive function were also demonstrated in college students with and without ADHD.³⁷ Furthermore, LDX was associated with reduced ADHD symptoms compared with placebo in a sample of college students and two different samples of adults.^37,61,62 Although higher doses of LDX related to greater improvement in the reduction of ADHD symptoms in two studies, in one study differences between doses were not observed.^37,61,62 The maintenance of efficacy of LDX compared with placebo during a 2-week randomized withdrawal phase was also demonstrated to be effective in a sample of adults with ADHD.⁶⁷ Finally, findings suggest that LDX may be effective for treating individuals with comorbid ADHD and depression or SUD and in reducing ADHD symptoms.⁶³

Table 1 Studies investigating the efficacy of lisdexamfetamine dimesylate (LDX) for adolescents and adults (N=9)

Reference	Measures	Doses of LDX	N	Groups	Design	Conclusion	Effect sizes
^Citation61	Clinician-determined ADHD-RS total score	30, 50, or 70 mg/day	N=420	Adults with ADHD	Double-blind, placebo-controlled study	All three LDX doses were more effective than placebo in the treatment of ADHD, with improvement in ADHD symptoms observed within 1 week. No differences between doses were observed	d=0.73, 0.89, and 0.99 for 30, 50, and 70 mg doses, respectivelya
^Citation35	BRIEF-A scales (GEC, index, and clinical subscales)	30, 50, or 70 mg/day	N=161	Adults with ADHD and EF deficits aged 18–55 years	Randomized, double-blind, placebo-controlled study	Individually optimized LDX intake was associated with improvement in EF	d for GEC =0.74a
^Citation66	AIM-A (quality of life measure) and CGI-S/CGI-I	30–70 mg/day	N=142	Adults with ADHD aged ≥18 years	4-week, open-label, dose-optimization phase followed by a randomized, double-blind, multicenter, placebo-controlled, 2-way crossover phase	Individually optimized LDX intake associated with increased quality of life	Not reported
^Citation67	ADHD-RS-IV, CGI-S	30, 50, or 70 mg/day	N=116	Adults with ADHD aged 18–55 years	3-week open-label phase at a stable LDX dose, 6-week double-blind, randomized, withdrawal phase on treatment with LDX (same dose) or placebo	Individually optimized LDX dose intake demonstrated maintenance of efficacy compared with placebo during a 2-week randomized withdrawal phase	Not reported
^Citation37	Self-report rating scales of functioning and direct assessment of ADHD symptoms, verbal learning/memory, and adverse side effects	30, 50, or 70 mg/day	N=50	College students with and without ADHD aged ≥18 years	Double-blind, placebo-controlled, crossover study	LDX intake was associated with large reductions in ADHD symptoms and improved EF compared with placebo. Higher LDX doses associated with greater symptom reduction and EF improvement	Effect of LDX on ADHD symptoms: partial η^Citation2=0.30 (inattention/memory problems) and 0.41 (hyperactivity/restlessness) and EF (global EF): partial η^Citation2=0.26
^Citation62	ADHD-RS, CGI-I, and CGI-IS	30, 50, or 70 mg/day	N=420	Adults with ADHD aged 18–55 years	4-week, randomized, double-blind, placebo-controlled, parallel-group, forced-dose titration study	LDX more effective than placebo at reducing ADHD symptoms; higher doses related to greater improvement; response not affected by prior pharmacotherapy	d for effect size of LDX relative to placebo ranged from ≈0.9 to 2.0, with stronger effects for greater baseline symptom severity
^Citation65	ADHD-RS-IV, CGI-I, and YQOL-R	30, 50, or 70 mg/day	N=314	Adolescents with ADHD aged 13–17 years	4-week, forced-dose titration, double-blind study	LDX at all doses was more effective than placebo in treating ADHD symptoms, with a trend for greater rates of improvement with increasing doses	Not reported
^Citation63	ADHD-RS, CGI-I	30, 50, or 70 mg/day	N=53	Adults with ADHD aged 18–55 years	Randomized, double-blind, placebo-controlled, forced-dose titration study	LDX was effective at treating ADHD symptoms among individuals with and without comorbid depressive or substance use disorders. No dosage effects were reported	d for LDX efficacy for participants without a history of depression =0.58 (CI −0.37, 1.53) and with a history of depression =0.86 (CI 0.57, 1.14)
^Citation64	PERMP-A and PERMP-C and ADHD-RS-IV	30, 50, and 70 mg/day	N=103 (initial N=142)	Adults with ADHD aged 18–55 years	Open-label dose-optimization and randomized, placebo-controlled, double-blind, 2-way crossover phases	Medium to large effect sizes of performance-based measures of productivity, suggesting attention increased as a result of individually optimized doses of LDX	Overall least-squares mean model-based effect sizes for LDX effect on PERMP-A =0.9 and PERMP-C =0.8

Note:

a Article did not report exact type of effect size, but based on calculations we interpreted it as Cohen’s d.

Abbreviations: ADHD, attention-deficit/hyperactivity disorder; ADHD-RS, ADHD Rating Scale; ADHD-RS-IV, ADHD Rating Scale IV; AIM-A, ADHD Impact Module for Adults; BRIEF-A, Behavior Rating Inventory of Executive Function-Adults; CGI-I, Clinical Global Impression-Improvement; CGI-S, Clinical Global Impression-Severity; CI, confidence interval; d, Cohen’s d; EF, executive function; GEC, Global Exeuctive Composite; LDX, lisdexamfetamine dimesylate; PERMP-A, Permanent Product Measure of Performance-Attempted; PERMP-C, Permanent Product Measure of Performance-Correct; YQOL-R, Youth QOL-Research Version.

The most common side effects reported by participants in studies investigating the efficacy of LDX included a decreased appetite, weight loss, dry mouth, insomnia, nausea, diarrhea, dizziness, headache, nasal congestion, feeling jittery, and anxiety. Mild to moderate adverse treatment-related effects were generally reported by 5% or fewer treatment group participants and included insomnia, tachycardia, irritability, fatigue, increased blood pressure/hypertension, upper respiratory tract infections, anxiety, decreased libido, and dyspnea. No deaths were reported in any of the studies. The results of most LDX studies led to the conclusion that the drug has a safety profile consistent with previous studies and other long-acting stimulants.

Efficacy of MPH and AMPH for adolescents and adults

Although research examining the efficacy of LDX is in its early stages, numerous studies have examined the efficacy of MPH, AMPH, and mixed amphetamine salts (MAS). The included research studies examined the effects of these stimulants among samples of adolescents (n=5), one of which also included children, and adults (n=15) (see Table 2). The vast majority of studies (n=14) specifically examined the effects of some form of MPH, whereas three studies examined MAS, and the remaining studies (n=3) examined a combination of MPH and MAS or AMPH. Regardless of the medication examined, all of the included studies reported statistically significant positive effects for stimulant medication compared with placebo, and effect sizes ranging from small to large based on Cohen’s estimates of effect size.⁶⁰ A total of 14 out of 20 included studies reported effect sizes. Of the studies reporting effect sizes for positive effects from stimulant medication, most effect sizes ranged from medium to large, with two studies reporting small to medium effects.^40,68–77 One study reported effect sizes regarding the interaction effects of differences between sex and medication dose, with no significant interactions found. Effect sizes ranged from very small (partial η2 as low as 0.00) to small.⁷⁸

Table 2 Studies investigating the efficacy of methylphenidate (MPH) and/or amphetamine for adolescents and adults (N=20)

Reference	Measures	Doses of medication	Types of medication	N	Age group	Design	Conclusion	Effect sizes
^Citation34	Adult ADHD Investigator Symptom Report Scale	36, 54, 72, 90, or 108 mg/day	OROS-MPH	N=226	Adults with ADHD aged 18–65 years	Randomized, placebo-controlled, double-blind, parallel group, dose-escalation study	OROS-MPH at 36–108 mg/day was effective at decreasing ADHD symptoms	Not reported
^Citation68	Digit span tasks, Raven’s Progressive Matrices, TOVA, decision-making tasks	15 mg (10 mg or 20 mg if low/high body weight)	MPH	N=58	Adults aged ≥18 years; 32 with ADHD, 26 non-ADHD	Randomized, double-blind, placebo-controlled study	MPH intake associated with enhanced cognitive performance, nonspecific to ADHD	d=0.74 for backward version of digit span task for MPH and placebo conditions, d=0.53 for forward version of digit span task for MPH and placebo conditions
^Citation83	CGI-I, Adult ADHD Investigator System Report Scale	Up to 1.3 mg/kg/day	OROS-MPH	N=141	Adults, with ADHD aged 19–60 years	Double-blind, randomized, 6-week, placebo-controlled, parallel design	MPH was effective at reducing symptoms of inattention and hyperactivity/impulsivity relative to placebo	Not reported
^Citation79	Wender–Utah Rating Scale, Adult ADHD Problem Behaviors, Hamilton Anxiety Rating Scale, Beck Depression Inventory, Wechsler Adult Intelligence Scale, Conners’ Continuous Performance Test, stop signal computerized task	10 mg 3 times daily then 15 mg 3 times daily	MPH	N=30	Adults with ADHD aged ≥18 years	Double-blind, placebo-controlled, crossover trial	MPH effective at improving ADHD symptoms compared with placebo	Not reported
^Citation40	ADHD-RS-IV	40, 60, or 80 mg/day	MPH-LA	N=725	Adults with ADHD aged 18–60 years	40-week, double-blind, randomized, placebo-controlled study	MPH-LA at doses of 40–80 mg/day decreased ADHD symptoms compared with placebo at the end of the 9-week double-blind phase of the study	d of all MPH-LA three dose levels combined was 0.55 for DSM-IV ADHD-RS (0.55, 0.47, and 0.64 for MPH-LA 40, 60, and 80 mg, respectively) and was 0.39 for SDS total score (0.47, 0.25, and 0.43 for MPH-LA 40, 60, and 80 mg, respectively)
^Citation69	CGI-I, CGI-IS, and CAARS self-report and observer rated	Participants were titrated to optimal effect over 1–3 weeks followed by 2 weeks of treatment on a stable dose	MLR MPH	N=50	Adults with ADHD aged 18–60 years	Double-blind, placebo-controlled, crossover study	Daily MLR MPH intake resulted in significant decrease in ADHD symptoms compared with placebo	Effect size for global improvement =0.90 (95% CI 0.43–1.36), effect size for the CAARS-A ADHD Index =0.53 (95% CI 0.05–0.99)a
^Citation80	ADHD-RS, semistructured and structured diagnostic interviews for ADHD and other disorders	0.5–1.0 mg/kg/day	MPH	N=45	Adults with ADHD aged ≥18 years	Randomized, placebo-controlled, double-blind, crossover trial	MPH demonstrated to be effective at reducing ADHD symptoms compared with placebo	Not reported
^Citation70	CAARS	18, 36, or 72 mg/day	OROS-MPH	N=402	Adults with ADHD aged 18–63 years	Double-blind, randomized, placebo-controlled, parallel-group, fixed-dose trial at 51 sites	OROS-MPH intake resulted in decrease in ADHD symptoms compared with placebo. Larger doses were associated with greater symptom reduction	d for the 18, 36, and 72 mg PR MPH groups was 0.38, 0.43, and 0.62, respectivelyb
^Citation78	ADHD self-report and parent report ratings, objective measures of inattention and hyperactivity/impulsivity during driving performance and neuropsychological tasks	72 mg of OROS-MPH, 30 mg of se-AMPH-ER	OROS-MPH, se-AMPH-ER	N=35	Adolescents with ADHD aged 16–19 years	Randomized, double-blind, placebo-controlled, crossover study	Efficacy of extended-release stimulants for treating ADHD symptoms found to be equivalent for males and females	Not reported
^Citation72	Structured diagnostic interview for DSM-IV (SCID-I and Kiddie SADS-E)	1.1 mg/kg/day	MPH	N=146	Adults with ADHD aged 19–60 years	Double-blind, randomized, placebo-controlled study	MPH was associated with reductions in ADHD symptoms compared with placebo	d=1.41 for the difference between MPH and placebob
^Citation73	ADHD-RS, CGI-I	10, 20, 30, and 40 mg/day	MAS-ER; Adderall XR	N=287	Adolescents with ADHD aged 13–17 years	4-week, randomized, multicenter, double-blind, placebo-controlled, parallel-group, forced-dose titration study	MAS-ER treatment for 4 weeks was associated with significant improvements in ADHD symptoms compared with placebo	d=0.78 for differences in ADHD symptomatology between MAS-ER and placebo groups
^Citation74	ADHD-RS, CGI-I	20, 30, or 40 mg/day	d-MPH-ER	N=184	Adults with ADHD aged 18–60 years	Multicenter, randomized, fixed-dose, double-blind, placebo-controlled	Higher doses of d-MPH-ER were associated with increased improvement in ADHD symptoms compared with placebo	d=0.53 for 20 mg, 0.49 for 30 mg, and 0.83 for 40 mg of d-MPH-ER
^Citation81	ADHD-RS-IV, CGI-I, Brown Attention Deficit Disorder Scale, and AIM-A	Starting dose 12.5 mg	Triple-bead MAS	N=272	Adults with ADHD aged 18–55 years	7-week, randomized, double-blind, multicenter, placebo-controlled, parallel-group, dose-optimization study	MAS was more effective in treating adult ADHD symptoms and improving executive functioning and QOL than placebo	24.5 versus placebo 5.7; P<0.0001, least-squares mean difference, 18.8 for performance and daily functioning subscale of AIM-A QOL between triple-bead MAS and placebo
^Citation75	ADHD-RS-IV, CGI-I and CGI-S, parent completed Weiss Functional Impairment Scale	10, 20, 25–30 mg/day	Long-acting d-MPH-ER and ER-MAS	N=56	Children and adolescents with ADHD aged 9–17 years, mean age 11.7 years	8-week, double-blind, crossover study comparing d-MPH-ER and MAS-ER	d-MPH-ER and MAS-ER were associated with significant reductions in ADHD symptoms. Improvement was associated with larger doses rather than type of medication	r^2= 0.59 and 0.46, respectively, for dose-related decreases in total and hyperactive symptom scores that did not differ by stimulant. r^2=0.11 for decreases of inattention symptoms that did not differ by stimulant
^Citation71	WRAADDS, ADHD Diagnostic Checklist, CAARS, CGI, and SDS	Two daily individually body weight-adjusted doses up to 1 mg/kg per day	MPH-ER	N=162	Adults with ADHD aged ≥18 years	Double-blind, randomized, placebo-controlled study with parallel-group design conducted at 10 sites	MPH-ER was more effective than placebo at treating ADHD symptoms in adults, based on both self- and investigator ratings	d=0.59 for differences between MPH-ER vs placebo. d=0.68 was reported for attention difficulties. Effects were also reported for hyperactivity d=0.51 and hyperactivity/impulsivity d=0.46
^Citation76	WRAADDS	10–60 mg/day	MPH-ER	N=249	Adults with ADHD aged ≥18 years	Multicenter, double-blind, randomized, placebo-controlled, 24-week study with parallel-group design	MPH-ER treatment in low to moderate doses was effective at reducing ADHD symptoms; effectiveness sustained at a 24-week follow-up	d=0.39 for overall ADHD symptoms. Significant treatment effects in favor of MPH-ER were found: inattention (d=0.41), hyperactivity (0.30), hot temper (0.33), affective lability (0.19), emotional overreactivity (0.45), disorganization (0.31), impulsivity (0.27)
^Citation77	WRAADDS, 6-item Emotional Lability Scale from the CAARS:S:L, Symptom Checklist-90-R	Medication was titrated twice/day for first 5 weeks by use of a flexible dose schedule to a maximum dose of 60 mg/day, starting with 10 mg/day. Minimum maintenance dose after 5 weeks was 20 mg/day	MPH-ER	N=363	Adults with ADHD aged ≥18 years	Randomized, multicenter, 24-week, double-blind, placebo-controlled study	MPH-ER was associated with improved emotional symptoms as well as obsessive–compulsive symptoms and problems with self-concept	d=0.37 for low MPH-ER treatment of inattention, hyperactivity, and impulsivity. Effects for the ITT and PP populations =0.30 and 0.46, respectively, for obsessive–compulsive symptomatology and 0.29 and 0.40 for self-concept
^Citation82	ADHD-RS and CAARS (short self-report)	20, 40, or 60 mg/day	MAS-ER	N=255	Adults with ADHD aged ≥18 years	Randomized, placebo-controlled trial	MAS-ER was effective at reducing ADHD symptoms, with effects lasting for up to 12 hours at a time. Symptom reduction was greatest for highest dose for those with severe symptoms	d for MAS-ER =0.8b
^Citation84	Investigator, parent, and adolescent assessments of ADHD-RS	18, 36, 54, or 72 mg/day	OROS-MPH	N=177	Adolescents with ADHD aged 13–18 years	Multisite study; 1-week washout phase, an open-label dose titration phase lasting up to 4 weeks, a 2-week double-blind phase consisting of a randomized comparison of an OROS-MPH vs placebo, and 8-week open-label follow-up safety phase of OROS-MPH	OROS-MPH (individually titrated) was found to significantly reduce ADHD symptoms among adolescents compared with placebo	Not reported
^Citation85	Go/no-go task measuring inhibition and the Delayed Matching-to-Sample task (nonexecutive visual memory)	72 mg OROS-MPH, 30 mg Adderall XR	OROS-MPH or se-AMPH-ER (Adderall XR)	N=35	Adolescents with ADHD aged 16–19 years	Randomized, double-blind, placebo-controlled study	Intake of both OROS-MPH and AMPH-ER was associated with improved neuropsychological functioning compared with placebo	Not reported

Notes:

a Article did not report exact type of effect size or calculations;

b article did not report exact type of effect size, but based on calculations we interpreted it as Cohen’s d.

Abbreviations: ADHD, attention-deficit/hyperactivity disorder; ADHD-RS, ADHD Rating Scale; ADHD-RS-IV, ADHD Rating Scale IV; AIM-A, ADHD Impact Module for Adults; CAARS, Conners’ Adult Attention Deficit Disorder Scale; CAARS:S:L, Conners’ Adult ADHD Rating Scale: Self-report: Long; CGI-I, Clinical Global Impression-Improvement; CGI-S, Clinical Global Impression-Severity; CI, confidence interval; d, Cohen’s d; d-MPH-ER, dexmethylphenidate extended release; DSM-IV, Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition; OROS, osmotic release oral system; MAS, mixed amphetamine salts; MAS-ER, mixed amphetamine salts extended release; MLR, multilayer release; MPH, methylphenidate; MPD-ER, methylphenidate extended release; MPH-LA, methylphenidate long acting; QOL, quality of life; SADS-E, Schedule for Affective Disorders and Schizophrenia - Epidemiologic version; SDS, Sheehan Disability Scale; SCID-I, Structural Clinical Interview for DSM-IV; se-AMPH-ER, extended-release amphetamine salts; TOVA, test of variables of attention; WRAADDS, Wender–Reimherr Adult Attention Deficit Disorder Scale; XR, extended release.

Studies assessing the effects of MPH, dextroamphetamine extended release (d-MPH-ER), MPH long-acting or extended release (MPH-ER), multilayer-release MPH, and MAS, including triple-bead MAS and MAS extended release (MAS-ER), have demonstrated reductions in ADHD symptoms among adult samples.^{34,40,69–72,74–76,79–82} For example, Biederman et al⁸³ reported that adults with ADHD taking osmotic release oral system (OROS)-MPH, compared with those taking a placebo, demonstrated reduced symptoms of inattention and hyperactivity/impulsivity specifically. Adolescents taking MAS-ER and MPH-ER have also been shown to demonstrate reduced ADHD symptoms.^73,84

Regarding the effective dose for improvements in ADHD symptoms, doses of MPH-ER of 36–108 mg/day and 40–80 mg/day have been shown to be effective.^34,40 Similarly, two studies reported that higher doses of MPH-ER and d-MPH-ER were more effective than lower doses at reducing ADHD symptoms among adults with ADHD.^70,74 Among adolescents, higher doses, compared with lower doses, of d-MPH-ER and MAS-ER have also been shown to relate to improvement of ADHD symptoms.⁷⁵ Rösler et al,⁷⁶ however, reported that even at low to moderate doses (10–60 mg/day), MPH-ER was effective at reducing ADHD symptoms and that these effects were sustained during a 24-week follow-up.

In addition to ADHD symptoms, studies have shown that MPH and MPH-ER may improve cognition and emotional symptoms, and triple-bead MAS may enhance executive functions and quality of life among adults.^68,77,81 For example, Rösler et al⁷⁷ reported on a multicenter 24-week study and found that among a sample of adults with ADHD, taking MPH-ER was associated with improvement in emotional symptoms, obsessive–compulsive symptoms, and problems with self-concept. Among adolescents, one study reported that within a sample of 35 adolescents, those taking either OROS-MPH or amphetamine extended release (AMPH-ER) (Adderall XR) demonstrated improved neuropsychological functioning compared with those taking placebo.⁸⁵ Finally, MPH-ER and AMPH-ER have been demonstrated to be equally effective at improving symptoms among male and female adolescents with ADHD.⁷⁸

Regarding side effects in studies investigating the efficacy of D-AMP and MPH, participants most commonly reported decreased appetite, weight loss, headache, insomnia, abdominal pain, dizziness, nervousness, emotional lability, and dry mouth. Approximately half of the studies (n=12) found that a majority of participants reported at least one side effect; however, mild to moderate adverse treatment-related effects were generally reported by ≤5% treatment group participants and included decreased weight, insomnia, tachycardia, palpitation, irritability, fatigue, increased blood pressure/hypertension, and anxiety. No deaths were reported in any of the studies. The results of most stimulant studies led to the conclusion that the drug has a safety profile consistent with previous research.⁸⁶

Stimulant misuse among adolescents and adults

The efficacy of prescription stimulants among adolescents and adults with ADHD has been well documented, but the effects of these medications among populations without ADHD are unclear. Despite a lack of empirical evidence of stimulant effectiveness in individuals without ADHD, numerous studies have documented the misuse of prescription stimulants among college students without the disorder. Indeed, the present review retrieved more research studies pertaining to stimulant misuse (n=47) than the combined number of included studies assessing the efficacy of LDX, MPH, AMP, and MAS combined (see Table 3). The primary foci of the retrieved studies examining stimulant misuse varied. For example, some studies reported on prevalence rate estimates, others examined characteristics of individuals most susceptible to stimulant misuse, and others reported primarily on student opinions, such as ethical implications of stimulant misuse. Most of the studies, however, reported on some combination of these factors. Therefore, a systematic assessment and inclusion of effect sizes was beyond the scope of the present article.

Table 3 Illicit stimulant use and misuse by adolescents and adults (n=47)

Reference	Measures	Stimulant description	N	Conclusion	Participants	Prevalence (lifetime if not otherwise indicated)
^Citation94	Monitoring the Future survey	Adderall	N=21,137	High-contact sports may influence male students to misuse stimulants as performance enhancers either on or off the playing field	Adolescents aged 13–17 years
^Citation128	Self-report ratings scales of substance use, stimulant use, and ADHD symptoms, Sensation Seeking Scale, Frost Multi-Dimensional Perfectionism Scale	Prescription stimulants	N=1,153	Nonmedical and medical misusers had a higher prevalence of using and combining other substances, as well as greater reports of side effects compared with appropriate users	Undergraduates aged 18–25 years
^Citation47	Internal Restlessness Scale, Depression Anxiety Stress Scales-21, Stimulant Survey Questionnaire	Adderall, Ritalin	N=1,033	Students who were members of fraternities and sororities reported higher rates of misuse compared with nonmembers	Undergraduates aged ≥18 years; fraternities and sorority members	19.8%
^Citation100	Self-report rating scales of weight loss behaviors, motivations for weight loss, stress-related eating, self-esteem, and eating disorder symptoms	Adderall, Ritalin	N=705	College students may be misusing stimulants for weight loss, which may be related to other problematic weight loss strategies	Undergraduates	11.7% (misuse to lose weight)
^Citation93	National Survey on Drug Use and Health	Adderall, Ritalin, Dexedrine, MPH, dextroamphetamine	N=443,041	Misuse of stimulants appears to be adopted by individuals already engaged in broader patterns of drug abuse and nonmedical use	Adolescents and adults aged ≤12 years	3.4%
^Citation117	Stimulant Survey Questionnaire, Perceived Stress Scale, Sensation Seeking Scale, National College Health Assessment	Ritalin, Concerta, Metadate, Adderall, Dexedrine	N=165	Students with ADHD reported higher rates of both prescription stimulant use and misuse compared with students without ADHD	Undergraduates aged ≤18 years; ADHD	11.5% occasionally misuse; 1.4% frequently misuse
^Citation44	Brief Symptom Inventory, Internal Restlessness Scale, Sensation Seeking Scale, Stimulant Survey Questionnaire	Ritalin, Concerta, Metadate, Adderall, Dexedrine	N=390	College students who reported misusing had higher levels of internal restlessness and psychological distress compared with those who did not report misuse. No significant difference was found between sex and stimulant misuse	Undergraduates aged ≥18 years	7.5% (past month)
^Citation89	Structured face-to-face interview, self-report rating scale of ADHD symptoms	MPH	N=66	Misuse of MPH was associated with other illicit substance use and diversion among a sample of adults with prescriptions for stimulant medication	Adults aged ≥18 years	29%
^Citation102	Drug Abuse Screening Test, self-report ratings of nonmedical use of prescription stimulants, past year other drug use, routes of administration	Ritalin, Dexedrine, Adderall, Concerta, MPH	N=3,639	College students who reported misusing prescription stimulants were more likely to report using other substances compared with nonmisusers. Sex not significantly associated with misuse	Undergraduates	8.5% (lifetime); 6.0% (past year)
^Citation129	National Survey on Drug Use and Health	Adderall, Ritalin, Dexedrine, Cylert, DextroStat, Concerta, MPH, dextroamphetamine	N=114,241	Past-year prescription stimulant misuse was more prevalent among persons aged 12–25 years and among whites. Prevalence in large metropolitan areas was lower than, or similar to, that in less populated areas. About 13% of past-year stimulant misusers met the survey criteria for dependence or abuse	Adolescents and adults aged ≤12 years	1.4% (past year)
^Citation118	Structured face-to-face interview	MPH	N=100	College students who reported misusing MPH were more likely to report using other substances compared with nonmisusers	College students
^Citation92	Self-report ratings of prescribed stimulant use, diversion of prescribed stimulants, illicit use of prescribed stimulants, heavy episodic drinking, monthly alcohol use, monthly cigarette use, annual marijuana use, annual ecstasy use	Ritalin, Dexedrine, Adderall	N=1,536	Students who reported prescription stimulant misuse reported significantly higher rates of alcohol and other drug use. Prescription stimulant misuse was more prevalent among students with no plans for college	Adolescents aged 10–17 years	4.5%
^Citation84	Schedule for Affective Disorders and Schizophrenia for School-Age Children-Epidemiologic Version, Structured Clinical Interview for DSM-IV, self-report questionnaire about stimulant medication misuse and diversion	Stimulants	N=98 (ADHD n=55; no ADHD n=43)	Although the majority of participants with ADHD used their medications appropriately, these participants misused and diverted (11%) their prescription medications at higher rates than participants without ADHD in a sample of adults taking prescribed medications. All of the participants with ADHD who diverted their medication and 83% of those who misused their medications were comorbid for conduct disorder or substance use disorder. Immediate-release stimulants (MPH and mixed amphetamine salts) were the most common medications. Participants with ADHD reported misusing/diverting; however, extended release was not as prevalent in the included sample	Adolescents and adults; ADHD	22% (participants with ADHD diagnosis)
^Citation130	Pittsburgh Sleep Quality Index	Ritalin, Adderall, Dexedrine, DextroStat, Provigil, Nuvigil, MPH, mixed-salt amphetamines, dextroamphetamine, modafinil	N=492	College students who reported nonmedical use of prescription stimulants reported worse subjective and overall sleep quality, as well as more sleep disturbance compared with nonusers	Undergraduates aged ≥18 years	14.4%
^Citation111	Questions about ADHD treatment and misuse and diversion of prescribed ADHD medication, side effects reported by PCPs, the Adult ADHD Self-Report Scale, and the Sheehan Disability Scale	ADHD medication	N=115	<1% of physicians suspected adults of diversion and 1.9% of adults reported diversion of stimulant medication. There was a high level of agreement between adult patients’ report and level of PCP distrust regarding use of taking a higher dose of ADHD drug than prescribed (79.7%) and use of ADHD drug combined with illegal substances (90.5%)	Adults; ADHD
^Citation108	Self-report questionnaire with mostly closed-ended, multiple-choice questions about student misuse of prescriptions drugs, motivation for nonmedical use, deceptive practices, frequency of use, consequences of nonmedical use, peer group nonmedical use, and an ethics-probing vignette	Adderall, Focalin, Dexedrine, Desoxyn, Ritalin, Methylin, Metadate, Concerta, Provigil	N=372	The majority of misusers endorsed taking prescription stimulants to enhance alertness or energy (65.9%) or improve academic performance (56.7%). More than half (55.8%) of the students perceived stimulant misuse to be academically dishonest and more than half (59.9%) believed that it offers an unfair academic advantage	Medical, pharmacy, and respiratory therapy undergraduate and graduate students	11.3%
^Citation119	Student Life Survey; Adult Symptom Rating Scale; Cut Down, Annoyed, Guilty, Eye-opener instrument; Drug Abuse Screening Test Short Form	Ritalin, Dexedrine, Adderall, Concerta, MPH	N=1,738	College students who reported misusing prescription stimulants were more likely to report cigarette smoking, binge drinking, and illicit use of cocaine	Undergraduates aged ≥18 years; past-year prescribed stimulant users	40% (past year)
^Citation97	Self-report survey that included questions about smoking status, illicit drug use, and misuse of prescription stimulant medications	Adderall, Adderall XR, Ritalin, Ritalin LA, Concerta, Focalin, Focalin XR, other	N=545 (ADHD n=486)	The most common specific medications were Adderall, Adderall XR, and Ritalin. Short-acting agents were the most commonly abused substances, indicating that the rate of delivery may influence the abuse potential of stimulants (immediate release may have more potential for abuse than extended release)	Adolescents and adults aged ≥13 years; ADHD	14.3%
^Citation109	Questionnaire of students’ experiences, perceptions of stimulant medication use at their institution, and use of stimulant medication for nonmedical reasons	Adderall, Ritalin, MPH	N=243	70% of dental and dental hygiene students reported nonmedical use of prescription stimulants to improve attention and/or concentration. The most commonly reported stimulant medication used nonmedically was Adderall (77%). 87% of the students obtained the medication through friends, and 90% began using the drug in college	Adults aged ≥18 years; dental and dental hygiene students	12.4%
^Citation112	Student Life Survey, self-report ratings of medically prescribed use of stimulant medication, illicit use of prescription stimulants, diversion of prescription stimulants, obtaining prescription stimulants, binge drinking, monthly alcohol use, annual marijuana use	Ritalin, Dexedrine, Adderall, Concerta	N=9,161	Risk factors for illicit use of prescription stimulants include being male, white, a member of a social fraternity or sorority, Jewish religious affiliation, and having a lower GPA	Undergraduates aged ≥18 years	8.1% and 5.4% (past year)
^Citation57	Adult ADHD Self-Report Scale, face-to-face interview, self-administered questionnaires	Adderall, Ritalin, Concerta	N=470	ADHD symptoms, particularly inattention, were associated with being a nonmedical user of prescription stimulants	Undergraduates aged ≥18 years
^Citation99	Self-report questionnaire about nonmedical use of prescription stimulants and illicit use of stimulants	Methylphendate, amphetamines	N=1,547 (1,035 pre and 512 university)	Males and students with poor grades reported higher lifetime prevalence rates than females and students with good grades among the preuniversity students. Friends and relatives were the main sources for prescription stimulants and the mean age for first time was 16.6 years and 23.3 years for preuniversity and university students, respectively	Preuniversity students aged 18–21 years, undergraduates aged 20–48 years	1.29%, 0.26% (past year), and 0.06% (past month)
^Citation49	Center for Epidemiologic Studies Depression Scale, self-report ratings of nonmedical ADHD medication use, motivations for nonmedical ADHD medication use, perceived effects of nonmedical ADHD medication use, possible adverse consequences of nonmedical ADHD medication use, ADHD symptoms, nonmedical use of other medications, alcohol, tobacco, and drug use	ADHD medication	N=3,407	The most frequently reported motive of nonmedical use of ADHD medication was to enhance the ability to study. Students perceived nonmedical use to be beneficial despite frequent reports of side effects	Undergraduates	8.9% (since beginning college) and 5.6% (past 6 months)
^Citation48	Stimulant Medication Use Questionnaire	Ritalin, Concerta, Metadate, Methylin, Dexedrine, Adderall, Desoxyn, Cyclert	N=333	Compared with nonillicit users, illicit users reported more motives to use, less concern with ethics and safety of use, and greater perception of use as socially acceptable	Undergraduates	20%
^Citation103	Question survey	Adderall, Adderall XR, Concerta, Stratera, Ritalin, Dexedrine	N=1,550	College students who illicitly used prescription stimulants were more likely to use other drugs	College students aged ≥18 years	43% (participants without ADHD diagnosis)
^Citation91	National Survey of Drug Use and Health	Ritalin, Cylert, Adderall, Concerta	N=17,709	Adolescents who utilize mental health treatment and engage in marijuana use and other illegal drugs have significantly increased risk for past-year nonmedical prescription stimulant use	Adolescents aged 12–17 years	1.7% (past year)
^Citation113	Student Life Survey, self-report ratings of medically prescribed use of stimulant medication, illicit use of prescription stimulants, diversion of prescription stimulants, obtaining prescription stimulants	Ritalin, Dexedrine, Adderall, Concerta	N=9,161	The most frequently reported motives of illicit use of prescription stimulants were helping with concentration, increase alertness, and providing a high. Male students (9.3%) reported significantly higher lifetime rates than did females (7.2%). Lifetime rates were higher for white (9.5%) and Hispanic (8.9%) students than for African American (2.7%), Asian (4.9%), or other racial student groups (5.8%)	Undergraduate aged ≥18 years	8.1% and 5.4% (past year)
^Citation131	ADHD Rating Scale, Massachusetts General Hospital Liking Scale	OROS-MPH	N=558	In a sample of adolescents and adults with nicotine substance use disorder, adults rated OROS-MPH as more effective in treating ADHD, whereas adolescents reported feeling more depressed when taking OROS-MPH. Compared with adults, adolescents were more likely to report having lost pills, the number of pills lost, and the number of pills not returned	Adolescents aged ≥18 years; substance abuse disorder; smokers
^Citation110	Stimulant Medication Use Questionnaire	Ritalin, Adderall, Cylert, Dexedrine, Concerta	N=1,025 (ADHD n=486)	Motives of misuse or abuse of stimulant medication included improving attention, partying, and improving grades. Nearly all (96%) respondents who misused or abused and specified a stimulant indicated that Ritalin was their stimulant medication of choice, followed by Adderall (2%)	Undergraduate and graduate aged ≥17 years, ADHD	16.2%
^Citation96	Adolescent Drug and Alcohol Diagnosis	Adderall, Dexedrine, MPH, dextroamphetamine	N=450	Of adolescents in a substance abuse treatment center who reported nomedically using MPH or dextroamphetamine, 88% reported nonmedical use of MPH. Abusers were less likely to be attending school and increased likelihood of having a concurrent eating disorder	Adolescents aged 12–18 years; substance abuse disorder	23%
^Citation52	Recreational Stimulant Use Survey	MPH, amphetamine salts	N=448	No statistically significant differences were found for sex or ethnicity in prevalence of stimulant misuse. 8% of students reported selling or giving away their prescription medication, 63% reported knowing someone who diverted their medication, and 67% reported knowing someone who had taken medication recreationally	Undergraduates aged ≥18 years	18%
^Citation95	Structured face-to-face interview	MPH, dextroamphetamine	N=162	In a sample of adolescents in an addiction treatment setting, patients with a diagnosis of ADHD more likely to have a lifetime history of stimulant abuse than those with no ADHD diagnosis	Adolescents aged 13–20 years; substance abuse disorder; ADHD
^Citation105	Self-report questionnaire including demographic questions, MPH information-related questions, questions about frequency of MPH use, and questions about perceptions of MPH rise in use	MPH	N=310	Iranian medical students reported relatively low levels of knowledge about MPH; however, increased time at university was associated with increased knowledge of MPH. Men demonstrated higher rates of MPH use than women and medical students with lower GPA were more likely to use MPH illegally than those with higher GPAs. Increased concentration was cited as the most common reason for MPH use	Adults aged 18–28 years; medical students	8.7%, 6.5% (past year), and 1% (past month)
^Citation104	Prescription Stimulant Expectancy Questionnaire, Sensation Seeking Scale, self-report rating scale of symptoms of ADHD	Adderall, Ritalin	N=42	Among a sample of students with prescriptions for stimulants, of those who reported misusing, 62.8% reported taking a higher dose than prescribed. Compared with nonmisusers, misusers of prescription stimulants were more likely to use a greater number of illicit substances, and reported higher hyperactivity symptoms and sensation seeking	Undergraduate; ADHD	45.2%
^Citation54	Question survey, face-to-face interview	Adderall	N=1,811	Most illegal users reported using ADHD stimulants primarily in periods of high academic stress and found them to reduce fatigue while increasing cognition and memory	College students	34% (participants with no prescription for ADHD medication)
^Citation56	Face-to-face interview	Prescription stimulants	N=1,253	Among students across 4 years of college, frequency of past-year nonmedical use of prescription stimulants was stable over time, averaging 11.3 days (SD =15.3) in year 2, 12.1 days (SD =20.8) in year 3, and 13.8 days (SD=24.2) in year 4. The main motive for nonmedical use of prescription stimulants was studying. Nonmedical use of prescription stimulants was associated with lower GPA and alcohol/cannabis disorders	College students aged 17–19 years	13.3% at year 1 and 31% by year 4
^Citation88	Computer-assisted personal interview, audio computer-assisted self-interview	Adderall, Ritalin, MPH	N=68,736	Adults (aged 26–34 years) and whites reported having misused stimulants more than other age and racial groups. Ritalin and other methylphenidates were misused at higher rates than Adderall	Adolescents and adults aged ≥12 years	7.1%
^Citation116	Self-report questionnaire, UPPS-P Impulsive Behavior, Alcohol Use Disorders Identification Test	Prescription stimulants	N=206	Nonmedical use of prescription stimulants was associated with increases in lack of premeditation, sensation seeking, positive expectancies, and positive evaluations	Undergraduates aged 18–24 years
^Citation106	Question survey of ADHD diagnosis, treatment history and nonmedical use of prescription stimulants	Methylphendate, amphetamine salts	N=388	Medical students appear to be a relatively high-risk population for nonmedical prescription stimulant use	Adults; medical students	10.1%
^Citation58	Patient Health Questionnaire, self-report ratings of nonmedical use of prescription stimulants, routes of administration	Ritalin, Dexedrine, Adderall, Concerta, MPH	N=3,639	Of the participants who reported nonmedical use of prescription stimulants, 39.2% used on 1–2 occasions, 31.6% used on 3–5 occasions, 11.3% used on 6–9 occasions, and 17.9% used on ≥10 occasions. Respondents who misuse frequently (51.4%) or nonorally (47.7%) had the highest rates of depressed mood in the past month	Undergraduates aged 18–25 years	6% (past year)
^Citation90	Question survey	Adderall, Ritalin, Dexedrine, MPH, dextroamphetamine, mixed-salts amphetamines	N=307	Fraternity members who reported nonmedical use of prescription stimulants were significantly higher among upper classmen, those living off-campus, and those who regularly smoked marijuana	College students; fraternity members	55%
^Citation114	National Survey on Drug Use and Health	Ritalin, MPH	N=23,645	Nonmedical prescription stimulant use was associated with psychological distress, sensation seeking, binge drinking, and college enrolment	Adults aged 18–25 years
^Citation98	Standard self-report measures of substance use	Adderall, Concerta, Ritalin, Dexedrine	N=4,572	White students (11.3%) reported significantly higher rates of lifetime stimulant misuse than African American (3.0%) or Hispanic (5.6%) students. The odds of substance use behaviors were greater among nonmedical stimulant users compared with medical users or individuals who indicated never using stimulant medication	High school seniors	9.5%
^Citation115	Self-report survey addressing stress, wellness, and coping, questions about psychostimulant use, and wastewater samples collected for 72-hour periods at 1-hour intervals at three time points from four residence halls comprising 476 undergraduate students	Adderall, Ritalin, or other ADHD medication	N=627; 468; 400 (first week of classes, midterms, finals, respectively)	Self-report of psychostimulant use and psychostimulant use measured via campus wastewater samples were significantly increased during periods of stress (midterms) compared with the first week of school	Undergraduate students	11.7% (Adderall), 8.5% (Ritalin), 5% (both)
^Citation107	Web-based survey about cognitive enhancement drug use	Amphetamines, other psychostimulants	N=1,115	11% of students reported using prescription psychostimulants during medical school. First experiences were most commonly reported in college (57%) and in medical school (22%). Psychostimulant use was associated with being male and other drug use. Although half of the sample perceived using psychostimulants for academic performance enhancement to be a problem, 21% did not perceive it to be a problem. The majority (95%) of students reporting using psychostimulants believed that academic standing could be improved by taking psychostimulants	Adults aged 20–49 years; medical students	18%
^Citation53	Web-based survey	Ritalin, Concerta, Metadate, MPH	N=2,087	College students reported using MPH nonmedically for recreational reasons as well as to improve academic performance. 53% of the nonmedical users were male. Nearly 74% of nonmedical users were white	College students aged 18–24 years	5.3%
^Citation87	Web-based survey	Prescription stimulants, ADHD medications	N=4,297	Of participants aged 18–25 years, 4.3% reported nonmedical use of ADHD medication compared with 1.3% among those aged 26–49 years. Friends and family members were the most reported source of ADHD medication for respondents who did not have a prescription. The most frequently reported motive of illicit use of prescription stimulants was productivity (40%), followed by staying awake (23%)	Adults aged 18–49 years	7.1% and 2% (past year)

Abbreviations: ADHD, attention-deficit/hyperactivity disorder; DSM-IV, Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition; GPA, grade point average; LA, long acting; MPH, methylphenidate; OROS, osmotic release oral system; PCP, primary care physician; SD, standard deviation; UPPS-P, urgency, premeditation, perseverance, sensation seeking, and positive urgency; XR, extended release.

The studies reviewed indicate that prescription stimulant misuse is a growing problem across adolescent and adult populations. Estimates of lifetime prevalence range from 7.1% to 29% among adults, 5.3% to 55% among college students, and 1.7% to 4.5% among adolescents.^53,87–92 Although estimates of stimulant misuse prevalence appear to be relatively low among general adolescent samples, estimates of stimulant misuse among adolescents using other substances (23%–31%) and among adolescents and adults receiving treatment for ADHD (14%) are much higher.^91–97 Estimates of lifetime stimulant misuse also appear to increase as adolescents reach higher grade levels. For example, among high school seniors, McCabe and West⁹⁸ reported that nearly 10% admitted to using prescription stimulants nonmedically at least once. Similarly, lifetime prevalence estimates in college have been shown to grow as students reach their final years of school. Garnier-Dykstra et al⁵⁶ reported that although only 13.3% of first year students reported stimulant misuse, by their fourth year 31% reported misuse.

In addition to college level, lifetime estimates of stimulant misuse may vary according to several other variables. For example, prevalence of stimulant misuse specifically for cognitive enhancement was estimated to be <2% in a sample of preuniversity (students preparing to attend university) and university students in Germany, but prevalence estimates of stimulant misuse for the purpose of weight loss has been reported to be nearly 12%.^99,100 Studies assessing stimulant misuse among general samples of college students have reported rates between approximately 8% and 34%.^54,101,102 Much higher estimates of stimulant misuse have been reported among samples of college students with ADHD (43%) or with prescriptions for stimulant medication (45.2%). The highest estimates of prevalence of stimulant misuse among college students (55%), however, have been reported among a sample of fraternity members.^90,103,104

Among medical students, lifetime prevalence estimates for engaging in prescription stimulant misuse have ranged between 9%–10% and 18%.^105–107 Moderate lifetime prevalence estimates of stimulant misuse have also been reported among undergraduate and graduate health care students (11%), dental and dental hygiene students (12.4%), and general samples including both undergraduate and graduate students (16.2%–17.5%).^50,108–110

Compared with adolescents and college students, very few studies have addressed prevalence estimates of stimulant misuse among adults aged ≥18 years outside of the university setting. Novak et al⁸⁷ reported that 2% of the 4,297 adults sampled indicated that they had engaged in nonmedical use of ADHD medications in the past year and 7.1% in their lifetime. Pilkinton and Cannatella⁸⁸ reported similar rates (7.1%) for lifetime prevalence estimates among a sample of both adolescents and adults. However, estimates of stimulant misuse prevalence among adults with prescriptions for stimulant medications have yielded much higher rates (29%), similar to adolescent populations.⁸⁹ Finally, Lensing et al¹¹¹ explored physician and adult patient agreement regarding prescription stimulant misuse and diversion and found that <1% of physicians suspected their patients of diversion and <2% of the adults themselves reported diversion of prescription stimulants, yielding a high level of agreement between the two.

Studies examining characteristics of students engaging in stimulant misuse have yielded relatively consistent findings regarding sex and race/ethnicity. Although multiple studies reported that male students have indicated higher rates of lifetime stimulant misuse than female students in university settings, several studies have also failed to find differences between males and females among college students and high school senior students.^{44,52,98,99,101,105,107,110,112} These conflicting findings may be due to differences in measurement. For example, although Franke et al⁹⁹ reported sex differences in lifetime prevalence of stimulant misuse for cognitive enhancement, the researchers did not find differences across males and females in past year or past month stimulant misuse. On the other hand, the vast majority of studies examining racial and ethnic differences related to stimulant misuse have reported that young adults, college students, and adults who are white are more likely to misuse stimulants than students of other races and ethnicities.^{49,53,88,91,98,99,101,113} Only one study reported that there were no differences in ethnicity regarding prevalence of stimulant misuse; however, <12% (n=37) of the study’s sample included students of color, limiting statistical power and thus conclusions regarding differences in prevalence among ethnic differences.⁵²

Interestingly, studies examining characteristics of adolescents who partake in nonmedical stimulant use indicate that students without plans to attend college have been shown to report a higher prevalence of stimulant misuse than those who plan to attend college, and adolescents who report prescription stimulant misuse may be less likely to attend school.^94,96 However, college students appear to be particularly vulnerable to stimulant misuse, and members of fraternities and sororities have reported higher rates of misuse than students unaffiliated with Greek organizations.^47,101,114 One of the reviewed studies found that college students who are upper classmen or live off-campus may be more likely to engage in nonmedical stimulant use.⁹⁰ Additional correlates of stimulant misuse among college students have included affiliation with a Jewish religion, perceiving stimulant use as normative, and engaging in problematic weight loss strategies.^100,101,115 Weight loss, however, may not be unique to college students, as adolescent prescription stimulant misusers have been found to be more likely to have an eating disorder than students who did not misuse stimulants.⁹⁶ Finally, all types of students (adolescents, adults, and medical) performing worse academically appear to be more likely to engage in nonmedical prescription stimulant use.^{56,99,101,105} Indeed, this review found that the most commonly reported reasons university students take prescription stimulants are related to academics, and studies suggest that during periods of high academic stress, college students may be more likely to use prescription stimulants, as indicated by self-report measures and by measurements of stimulant levels in campus wastewater samples.^{49,54,56,105,108,110,113,115}

It is not surprising, then, that procrastination and difficulty with time management have also been shown to relate to stimulant misuse among college students.¹¹⁵ Further, stimulant misuse among college students has been shown to relate to higher levels of hyperactivity, sensation seeking, depression, internal restlessness, and psychological distress and lower levels of premeditation.^{44,58,104,114,116} ADHD diagnoses and symptoms may also relate to stimulant misuse. Adolescents, college students, and adults diagnosed with ADHD have reported higher levels of prescription stimulant misuse than students without ADHD, and ADHD symptoms have been shown to correlate with nonmedical use of prescription stimulants.^57,84,95,117 It is important to note, however, that studies suggest that the vast majority of individuals with ADHD do not misuse or divert their stimulant medications.⁸⁴

The studies included in the present review also indicate that in addition to ADHD, diagnoses of conduct disorder and SUD are associated with increased nonmedical prescription stimulant use and diversion in adolescents and adults.⁸⁴ Illicit drug use among adolescent and university students is also associated with misuse of prescription stimulants.^{52,56,90,91,93,98,101,103,104,107,115,118,119}

Several studies in the current review assessed student perspectives on prescription stimulant misuse, and findings revealed that students’ opinions on the ethical implications of taking illicit prescription stimulant medications to enhance academic outcomes are mixed. For example, Bossaer et al¹⁰⁸ reported that health care students were split between considering stimulant misuse to be academically dishonest and proffering unfair academic advantages. Similarly, half of the medical students sampled by Emanuel et al¹⁰⁷ perceived stimulant misuse to be a problem, but 20% did not. Students who report engaging in stimulant misuse, however, may feel less conflicted regarding ethical implications. For example, Judson and Langdon⁴⁸ reported that compared with nonillicit users, illicit users demonstrated fewer concerns regarding the safety and ethics of using stimulant medication.

Whether or not students consider their decision to engage in stimulant misuse to be ethical, students misusing stimulants appear to expect positive outcomes.^107,116 Indeed, students who have reported taking stimulant medications illicitly have endorsed feeling a reduction in fatigue and improvement in cognition and memory after taking prescription stimulants.⁵⁴ The present findings also indicate that students who misuse tend to perceive the benefits as outweighing the risks, despite the fact that little is known about the physiological and cognitive effects of prescription stimulant medications among populations without ADHD.⁴⁹ Two of the reviewed studies suggest that individuals misusing stimulants may be more likely to take short-acting agents than long-acting agents. Wilens et al⁸⁴ and Bright,⁹⁷ for example, reported that adolescents and adults were more likely to misuse short-acting agents than long-acting agents, suggesting that immediate-release agents have more potential for abuse. Results were mixed regarding the most commonly misused fast-acting stimulant, with Ritalin (MPH) more likely to be misused than Adderall among adults, but nearly 12% of college students reported misusing Adderall compared with 8.5% misusing Ritalin.^88,115

Discussion

Effectiveness of ADHD treatment options

Studies included in this review revealed that the medical use of prescription stimulants is efficacious in reducing ADHD symptoms and may improve cognitive and psychosocial outcomes in individuals diagnosed with ADHD. Specifically, research investigating LDX in comparison with placebo consistently found LDX efficacious across 30, 50, and 70 mg/day. Two studies, however, found that higher doses related to greater improvements in overall functioning.^37,62 Most notably, the present findings support that LDX is effective for reducing ADHD symptomatology across different ages.^37,61,62 Among adults with ADHD, LDX was also found to positively affect executive functions, quality of life, and performance productivity.^35,64,66 Additionally, LDX has been found to be effective in reducing ADHD symptoms with individuals with comorbid depression and SUD.⁶³ Although these results are encouraging, it is important to note that most studies did report negative side effects from LDX, such as decreased appetite, weight loss, and nasal congestion. More severe side effects, however, including tachycardia, increased blood pressure/hypertension, and anxiety, were reported by <5% of the included study samples, and no individuals died while participating in these studies.

Similar to those investigating LDX, studies examining the efficacy of MPH and D-AMP consistently found such treatment options to be associated with fewer ADHD symptoms compared with placebo. These positive effects were found among long-acting and short-acting stimulant medications, and one study reported similar effects for both males and females.⁷⁸ Although higher doses generally proved to be more effective at reducing ADHD symptoms, low to moderate doses of stimulants may also be effective at reducing ADHD symptomatology.^70,74,76 Such treatment options examined in this review were associated with enhanced cognitive performance, executive functioning, and quality of life and fewer emotional symptoms.^68,77,81 Although MPH and D-AMP have proved to be efficacious in treating ADHD symptomatology, it is important to consider their side effects that are similar to LDX: decreased appetite, weight loss, headache, insomnia, abdominal pain, dizziness, nervousness, emotional lability, and dry mouth. Although rare, more severe side effects of these medications have included psychosis, seizures, and cardiac events such as tachycardia, hypertension, myocardial infarction, and sudden death.¹²⁰

Overall, however, these results are consistent with the child literature indicating that prostimulant and stimulant medications, when used as prescribed, are a safe and efficacious treatment option for improving attention and decreasing hyperactivity and impulsivity symptoms.^{23,34–38,40–42} What remains less clear, however, is whether these medications affect academic and work-related outcomes of adolescents and adults without ADHD. Although one study reported improvements in measured cognition from MPH and another found that students who misuse stimulant medication perceive positive academic effects,^54,68 none of the studies included in the present review examined changes in quality of work or student grade or productivity after taking stimulant medications. Given that cognitive enhancement-related reasons are considered the primary motivation for college students misusing prescription stimulant medications, future research examining the effects of prescription stimulants on direct measures of academic success (eg, studying and concentration, grade performance, quality of writing, and reading comprehension) is warranted.

An additional area that warrants attention concerns the efficacy of nonstimulant medication for the reduction of ADHD symptoms and any potential effects for cognitive enhancement. The present review was unable to identify any studies examining nonstimulant efficacy among adults and adolescents meeting the required eligibility criteria. Given the lower abuse potential associated with nonstimulant medication, use of these medications among populations more susceptible to diversion and misuse may be prudent.³² Such a recommendation, however, is contingent on a demonstration of the efficacy of nonstimulants among adolescent and adult populations most at risk for stimulant abuse.³²

Finally, although prescription stimulant medication is considered the front line of pharmacotherapy for ADHD treatment in adolescents and adults, these drugs have significant diversion and misuse potential.⁴³ In fact, the present review revealed that the medical use of prescription stimulants is associated with increased stimulant misuse among students with ADHD, with one study reporting misuse rates of 62.8% among participants with a valid prescription.¹⁰⁴

Stimulant misuse

Results from the present review indicate that a significant percentage of adolescents and adults are engaging in nonmedical stimulant misuse, which is consistent with previous research examining college students specifically.⁴⁵ Results revealed lifetime prevalence rates of stimulant misuse ranging from 1.7% to 55%, with reports varying across the population being examined.^90,91 A limitation of this body of literature is the dearth of studies investigating the prevalence of prescription stimulant misuse among college students outside of the US, which impedes cross-cultural comparisons regarding prescription stimulant misuse.

Similar to previous studies examining the nonmedical use of stimulants, the present review revealed that estimates vary according to numerous variables. For example, one trend that has emerged is that as individuals reach higher grade levels, they misuse at greater rates.^56,98 Although increased exposure to prescription stimulants may be one reason students report higher prevalence rates of stimulants as they increase in age, these findings suggest that prescription stimulants may also be misused more frequently as coursework becomes more challenging and academic success becomes more difficult to obtain. Indeed, as indicated in this review, academic performance has been reported as the primary motive for this behavior. A critical finding, however, is that prescription stimulant misuse has been found to be negatively associated with academic performance.^44,90,101 For example, Arria et al¹²¹ reported that college freshmen who used prescription stimulants nonmedically had poorer study skills (eg, skipped classes more often and spent less time studying and more time socializing) and poorer academic performance (GPA) in high school and college than students who did not endorse stimulant misuse.⁵¹

Despite the negative relationship between academic performance and stimulant misuse, most students who endorse the nonmedical use of stimulants perceive them as effective and helpful for enhancing their academic performance.⁴⁹ For example, Weyandt et al⁴⁴ found that >20% of students in their sample agreed or strongly agreed that the occasional nonmedical use of prescription stimulants is harmless. Additionally, stimulant misusers may be less concerned about the safety and ethical implications of stimulant misuse compared with students who do not misuse stimulants.⁴⁸ Findings suggest, however, that general student populations are conflicted about the ethical implications of stimulant misuse.

Although individuals without ADHD have endorsed positive effects from misusing stimulant medication, to date only one study has explored the effects of Adderall on college students without ADHD, and this study, in general, did not find enhancement of cognitive abilities, despite the students’ impression that it was improving their performance.¹²² Similar performance-enhancing impressions have been made of MPH, and have led to the popularity of its use among adolescents and college students with and without ADHD.¹²³ In addition, the present review suggests that adolescents and adults are more likely to misuse short-acting or immediate-release agents compared with long-acting agents.^84,97 Consistent with previous studies, the present review suggests that students who are white, affiliated with a fraternity or sorority, engaging in other illicit drugs, and male, are more likely to misuse prescription stimulants.^{47,49,56,57,84,89,92,94,96,101,102,113,118,124} Although some of the studies reported no sex differences, recently Weyandt et al⁴⁵ reported on the effect sizes of sex differences in studies examining stimulant misuse. Cohen’s d effects ranged from 0.88 to 5.38, suggesting that males are misusing at greater rates than females.^109,110,125

Implications

Pharmacotherapy is the principal choice of treatment for ADHD among children, adolescents, college students, and adults.^28,29 Because stimulants are the most frequently prescribed drug for college students with ADHD, and most college students with ADHD take prescription stimulants, more double-blind, placebo-controlled studies examining the effectiveness of these medications in college students are warranted.²² It is important to note, however, that there is recent evidence that prostimulants may also be effective at improving symptoms in individuals with ADHD.²⁸

The present review provides evidence that college students with ADHD and those with a stimulant prescription are taking part in greater levels of stimulant misuse compared with those without the disorder.^103,104 Although individuals with ADHD may greatly benefit from stimulant medication, these prescription medications have significant abuse potential when they are not used as prescribed.⁴³ All prescription stimulants that are used to treat ADHD are controlled substances; however, abuse liability varies based on the delivery system in which the medication activates.¹²⁶ For example, Svetlov et al¹²³ reported that although MPH and AMPH have similar psychopharmacological effects, they do have different neurochemical mechanisms of action. Such differences are essential to consider, as MPH appears to have less rewarding abilities, lowering its chances of dependence, especially when taken as prescribed. A second example includes the requirement of enzymatic hydrolysis for LDX before its therapeutic effects are achieved, which results in a slow increase of D-AMP levels, potentially lowering its use for diversion or misuse.^37,127 Indeed, recent research has examined the effects of LDX in a group of stimulant abusers who did not have ADHD, and found that intravenous doses of LDX had greater abuse-related disliking compared with placebo.¹²⁷ Specifically, Jasinski and Krishnan¹²⁷ administered 100 mg of LDX and 40 mg of D-AMP to individuals, also reporting that intravenous doses of D-AMP have significantly more abuse-related liking effects compared with placebo. Additionally, because of its chemical properties, LDX cannot be ground or dissolved into a short-acting stimulant, which has been the stimulant of choice for stimulant misusers. Given the demonstrated effects of LDX on improving ADHD symptomology, as well as executive function, and its demonstrated greater abuse-related disliking, LDX may be the ADHD medication of choice for college students with ADHD who are at risk for stimulant misuse.^37,127 LDX may also be a good choice for prescribers working with the college student population to help prevent stimulant diversion among valid prescription holders and misuse among college students without ADHD. Results of this review also suggest that health care providers should inform their patients of the health and legal risks associated with the misuse of prescription medications, and monitor the use of these medications on a frequent basis. Lastly, health care providers involved in prescribing ADHD-related medications should be thoroughly trained in the proper assessment, diagnosis, and treatment of ADHD to ensure diagnostic accuracy and treatment effectiveness.

In addition to educating prescribers about the rates of misuse and diversion, as well as the variables associated with stimulant misuse, it is critical that prevention and intervention efforts be made amongst health care providers and educators at the middle school, high school, and higher education levels. Further efforts should target particularly higher-risk college populations such as fraternities and sororities. Information regarding the potential side effects of stimulant medications taken at varying doses and by different methods (eg, snorting or injecting), in addition to side effects resulting from the ingestion of medication as prescribed, should be made available to students in particular. Students should also be informed of the dangers of coingestion of prescription stimulants with other substances (eg, alcohol and cocaine), and particular emphasis should be placed on maintaining security of their medication (eg, lockboxes). Students who are misusing prescription stimulants without medical guidance are placing themselves at health and psychological risk, in addition to legal consequences for buying, selling, and diverting their medications.¹²⁰

The inclusion of a psychoeducational component that focuses on inaccurate perceptions of safety surrounding nonmedical prescription stimulant use would be beneficial to intervention as well. Students who are at risk for stimulant misuse with academic problems can be provided with various support, such as tutoring and structured environments for studying and work completion. This additional support may encourage a school culture of clear expectations, educational support, and effective study habits, rather than competitiveness. For individuals who have been misusing stimulants or are inclined to misuse, it is imperative to discuss the motivating factors and determine any possibly undiscovered psychological, social, and/or emotional problems related to misuse or the desire to misuse. By pinpointing and addressing the core cause of stimulant use, students can be provided with the resources that will directly provide them with benefits and alternative methods to meet their specific needs. Thus, students should be educated about the potential side effects and risks associated with prescription stimulant misuse, as well as encouraged to access campus resources for academic and psychological support.^45,47

Conclusion

Results from the present review support that both stimulant and prostimulant medications (including LDX, MPH, AMPH, and MAS), when used as prescribed, are safe and effective options for reducing ADHD symptoms in adolescents and adults with ADHD. Preliminary studies also suggest that prescription stimulants may improve psychosocial outcomes (eg, quality of life, self-concept, and obsessive– compulsive symptoms) for those with ADHD. Research explicitly examining effects of prescription stimulants on academic and cognitive functioning in students without ADHD is sorely limited, yet the current review revealed that alarmingly high percentages of adolescents and adults are engaging in nonmedical prescription stimulant use primarily for cognitive enhancement. Results of the present review also revealed a higher rate of prescription stimulant misuse among individuals with ADHD compared with individuals without the disorder, and that short-acting agents are more likely to be misused than long-acting agents. These findings emphasize the need for additional research concerning the misuse of prescription stimulants and have direct implications for prevention and intervention efforts to reduce prescription stimulant misuse among adolescents and young adults.

Acknowledgments

Research reported in this publication was supported by the National Center for Research Resources of the National Institutes of Health under Award Number G20RR030883. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Disclosure

The authors report no conflicts of interest in this work.