Cochrane for Clinicians
Putting Evidence into Practice
Amphetamines for Attention-Deficit/Hyperactivity Disorder in Adults
Am Fam Physician. 2012 Sep 1;86(5):413-415.
A 36-year-old man who is enrolled in a master's degree program presents to your office stating that he is having difficulty focusing and concentrating on class material, and is afraid he will not be able to graduate. He reports a history of attention-deficit/hyperactivity disorder (ADHD) that was successfully treated with amphetamines in middle and high school. You wonder if this patient would benefit from amphetamines as an adult.
Are amphetamines effective for the treatment of adult ADHD?
Amphetamines improve ADHD symptom severity but, when compared with placebo, they are associated with increased discontinuation rates because of adverse effects. There does not appear to be a difference among dosages or between the immediate- and sustained-release formulations.1 (Strength of Recommendation: A, based on consistent, good-quality, patient-oriented evidence.)
Background: Attention-deficit/hyperactivity disorder (ADHD) is a childhood-onset disorder that can persist into adulthood. Amphetamines are used to treat adult ADHD, but uncertainties persist about their efficacy and safety.
Objectives: To examine the efficacy and safety of amphetamines for adults with ADHD, as well as the influence of dose, drug type, and release formulation type.
Search Strategy: The authors searched CENTRAL, PubMed, EMBASE, CINAHL, PsycINFO, ClinicalTrials.gov, UK Clinical Trials Gateway, and also references obtained from articles and experts in the field. The authors conducted the electronic searches on February 25, 2010.
Selection Criteria: Randomized controlled trials comparing the efficacy of amphetamine derivatives against placebo or an active intervention.
Data Collection and Analysis: Two authors extracted data from each of the included studies. The authors used the standardized mean difference (SMD) and the risk ratio (RR) to assess continuous and dichotomous outcomes, respectively. They conducted a stratified analysis to determine the influence of moderating variables. They assessed the trials for risk of bias and drew a funnel plot to investigate the possibility of publication bias.
Main Results: The authors included seven studies, which enrolled 1,091 participants. All studies were placebo-controlled and three included an active comparator: guanfacine, modafinil, and paroxetine. Most studies had short-term follow-up, with a mean study length of 8.1 weeks. Amphetamines improved ADHD symptom severity (SMD = –0.72; 95% confidence interval [CI], –0.87 to –0.57) but did not improve retention in treatment overall and were associated with an increased drop-out rate due to adverse events (RR = 3.03; 95% CI, 1.52 to 6.05). The three amphetamine derivatives investigated (dextroamphetamine, lisdexamphetamine, and mixed amphetamine salts) were all efficacious for reducing ADHD symptoms, but mixed amphetamine salts also increased retention in treatment. Different doses did not appear to be associated with differences in efficacy. The authors investigated immediate- and sustained-release formulations but found no differences between them on any outcome. When amphetamines were compared with other drug interventions, no differences were found. The authors did not find any study to be at low risk of bias overall, mainly because amphetamines have powerful subjective effects that may reveal the assigned treatment.
Authors' Conclusions: Amphetamines improved short-term ADHD symptom severity. Mixed amphetamine salts also increased retention in treatment. Amphetamines were associated with higher attrition due to adverse events. The short study length and the restrictive inclusion criteria limit the external validity of these findings. Furthermore, the possibility that the results of the included studies were biased was high, which could have led to an overestimation of amphetamine efficacy.
These summaries have been derived from Cochrane reviews published in the Cochrane Database of Systematic Reviews in the Cochrane Library. Their content has, as far as possible, been checked with the authors of the original reviews, but the summaries should not be regarded as an official product of the Cochrane Collaboration; minor editing changes have been made to the text (http://www.cochrane.org).
ADHD is a neurodevelopmental disorder that typically begins in childhood and often persists into adulthood. Adults may demonstrate both hyperactivity and inattention. Symptoms of inattention, such as difficulty sustaining attention, dislike of tasks requiring attention, and easy distractibility, are more common than hyperactive symptoms in adults with ADHD.2 The disorder affects an estimated 4.4 percent of adults in the United States,3 and has been associated with unemployment, divorce, depression, post-traumatic stress disorder, and substance abuse.4 Treatment has been associated with higher employment rates5 and reduced substance abuse.6 Some pharmacotherapies, notably bupropion (Wellbutrin), target ADHD and comorbid mood and anxiety disorders.7
This Cochrane review focused on the use of amphetamines (dextroamphetamine, lisdexamfetamine [Vyvanse], and mixed amphetamine salts) in seven trials with a total of 1,091 patients and a mean study length of 8.1 weeks.1 Amphetamines improved ADHD symptom severity when compared with placebo in five out of six studies; when results were pooled, the standardized mean difference with treatment was –0.72 (95% confidence interval [CI], –0.87 to –0.57). In the four studies that incorporated a Clinical Global Impression–Improvement scale, more patients taking amphetamines achieved a score of “very much improved” or “improved” than did those taking placebo (pooled risk ratio [RR] = 2.30; 95% CI, 1.84 to 2.87). In the six studies that evaluated treatment retention, amphetamines were not associated with improved retention (pooled RR = 1.06; 95% CI, 0.96 to 1.18); on the other hand, in two of four studies, amphetamines were associated with an increase in drop-out rates secondary to adverse effects (pooled RR = 3.03; 95% CI, 1.52 to 6.05).
Common adverse effects of amphetamine use included dry mouth, decreased appetite, insomnia, and headache, as well as an increase in heart rate and blood pressure.8–10 Because of the effect amphetamines had on cardiovascular parameters, caution should be exercised in patients with, or at high risk of, circulatory disease. Mixed amphetamine salts alone were associated with fewer treatment withdrawals in one of three studies; in the other two studies, there was a trend toward treatment retention (pooled RR = 1.19; 95% CI, 1.06 to 1.35).1
Most clinicians use the Diagnostic and Statistical Manual of Mental Disorders, 4th ed., text revision (DSM-IV–TR) criteria to diagnose ADHD in adults. However, the DSM-IV–TR criteria focus on childhood findings, which may not be present or may be attenuated in adults. Instead of reporting typical inattention and hyperactivity, adult patients may, through aging and maturation, report developmentally attenuated symptoms such as organizational problems, mood lability, and difficulties with home and social functioning. As a result, clinicians should take a thorough psychosocial history, look intently for clues to the diagnosis in the patients' early childhood recollections, and screen for DSM-IV–TR criteria that may have been diminished by normal adult maturation (e.g., eliciting a history of internal restlessness as opposed to external fidgeting).11
Amphetamines are one of several pharmaceutical options for adults with ADHD. The U.K. National Institute for Health and Clinical Excellence (NICE) Clinical Practice Guideline recommends methylphenidate (Ritalin; a nonamphetamine stimulant)—in conjunction with a comprehensive mental health, educational, and occupational treatment program—as first-line therapy for ADHD in adults. NICE also recommends that other stimulant medications, including amphetamines, be used if there are intolerable adverse effects or if there is a lack of effectiveness.12 The American Psychiatric Association and American Academy of Child and Adolescent Psychiatry ADHD Parents Medication Guide, although targeting children, echoes the NICE guidelines in listing methylphenidate, alone or in combination with behavioral therapy, first among pharmaceutical treatments for ADHD.13
1. Castells X, Ramos-Quiroga JA, Bosch R, Nogueira M, Casas M. Amphetamines for attention deficit hyperactivity disorder (ADHD) in adults. Cochrane Database Syst Rev. 2011(6):CD007813.
2. Kessler RC, Green JG, Adler LA, et al. Structure and diagnosis of adult attention-deficit/hyperactivity disorder: analysis of expanded symptom criteria from the Adult ADHD Clinical Diagnostic Scale. Arch Gen Psychiatry. 2010;67(11):1168–1178.
3. Polanczyk G, de Lima MS, Horta BL, Biederman J, Rohde LA. The worldwide prevalence of ADHD: a systematic review and metaregression analysis. Am J Psychiatry. 2007;164(6):942–948.
4. Kessler RC, Adler L, Barkley R, et al. The prevalence and correlates of adult ADHD in the United States: results from the National Comorbidity Survey Replication. Am J Psychiatry. 2006;163(4):716–723.
5. Halmøy A, Fasmer OB, Gillberg C, Haavik J. Occupational outcome in adult ADHD: impact of symptom profile, comorbid psychiatric problems, and treatment: a cross-sectional study of 414 clinically diagnosed adult ADHD patients. J Atten Disord. 2009;13(2):175–187.
6. Wilens TE. Impact of ADHD and its treatment on substance abuse in adults. J Clin Psychiatry. 2004;65 (suppl 3):38–45.
7. Verbeeck W, Tuinier S, Bekkering GE. Antidepressants in the treatment of adult attention-deficit hyperactivity disorder: a systematic review. Adv Ther. 2009;26(2):170–184.
8. Adler LA, Goodman DW, Kollins SH, et al.; 303 Study Group. Double-blind, placebo-controlled study of the efficacy and safety of lisdexamfetamine dimesylate in adults with attention-deficit/hyperactivity disorder. J Clin Psychiatry. 2008;69(9):1364–1373.
9. Spencer TJ, Adler LA, Weisler RH, Youcha SH. Triple-bead mixed amphetamine salts (SPD465), a novel, enhanced extended-release amphetamine formulation for the treatment of adults with ADHD: a randomized, double-blind, multicenter, placebo-controlled study. J Clin Psychiatry. 2008;69(9):1437–1448.
10. Weisler RH, Biederman J, Spencer TJ, et al. Mixed amphetamine salts extended-release in the treatment of adult ADHD: a randomized, controlled trial. CNS Spectr. 2006;11(8):625–639.
11. Haavik J, Halmøy A, Lundervold AJ, Fasmer OB. Clinical assessment and diagnosis of adults with attention-deficit/hyperactivity disorder. Expert Rev Neurother. 2010;10(10):1569–1580.
12. National Collaborating Centre for Mental Health Attention deficit hyperactivity disorder: diagnosis and management of ADHD in children, young people and adults. NICE clinical guideline 72. London, United Kingdom: National Institute for Health and Clinical Excellence (NICE); 2008. http://www.nice.org.uk/CG72. Accessed March 27, 2012.
13. American Psychiatric Association. ADHD Parents Medication Guide. http://www.psych.org/Share/Parents-Med-Guide/Medication-Guides/ParentsMedGuide-ADHD-English.aspx. Accessed October 12, 2011.
The Cochrane Abstract is a summary of a review from the Cochrane Library. It is accompanied by an interpretation that will help clinicians put evidence into practice. Drs. Saguil and Sheridan present a clinical scenario and question based on the Cochrane Abstract, followed by an evidence-based answer and a critique of the review. The practice recommendations in this activity are available at http://summaries.cochrane.org/CD007813.
The series coordinator for AFP is Kenneth W. Lin, MD, Department of Family Medicine, Georgetown University School of Medicine, Washington, DC.
A collection of Cochrane for Clinicians published in AFP is available at http://www.aafp.org/afp/cochrane.
Copyright © 2012 by the American Academy of Family Physicians.
This content is owned by the AAFP. A person viewing it online may make one printout of the material and may use that printout only for his or her personal, non-commercial reference. This material may not otherwise be downloaded, copied, printed, stored, transmitted or reproduced in any medium, whether now known or later invented, except as authorized in writing by the AAFP. Contact firstname.lastname@example.org for copyright questions and/or permission requests.
Want to use this article elsewhere? Get Permissions