TY - JOUR
T1 - Efficacy of a mixed amphetamine salts compound in adults with attention-deficit/hyperactivity disorder
AU - Spencer, Thomas
AU - Biederman, Joseph
AU - Wilens, Timothy
AU - Faraone, Stephen
AU - Prince, Jefferson
AU - Gerard, Kristine
AU - Doyle, Robert
AU - Parekh, Asha
AU - Kagan, Jake
AU - Bearman, Sarah Kate
PY - 2001
Y1 - 2001
N2 - Background: We report on a controlled trial of a mixed amphetamine salts compound (Adderall, dextroamphetamine sulfate, dextro-, levoamphetamine sulfate, dextroamphetamine aspartate, levoamphetamine aspartate, and dextroamphetamine saccharate) in the treatment of adult attention-deficit/hyperactivity disorder (ADHD). Methods: This was a 7-week, randomized, double-blind, placebo-controlled, crossover study of Adderall in 27 well-characterized adults satisfying full DSM-IV criteria for ADHD of childhood onset and persistent symptoms into adulthood. Medication was titrated up to 30 mg twice a day. Outcome measures included the ADHD Rating Scale and the Clinical Global Impression Score. Comorbid psychiatric disorders were assessed to test for potential effects on treatment outcome. Results: Treatment with Adderall at an average oral dose of 54 mg (administered in 2 daily doses) was effective and well tolerated. Drug-specific improvement in ADHD symptoms was highly significant overall (42% decrease on the ADHD Rating Scale, P<.001), and sufficiently robust to be detectable in a parallel groups comparison restricted to the first 3 weeks of the protocol (P<.001). The percentage of subjects who improved (reduction in the ADHD rating scale of ≥30%) was significantly higher with Adderall treatment than with a placebo (70% vs 7%; P=.001). Conclusions: Adderall was effective and well tolerated in the short-term treatment of adults with ADHD. More work is needed to evaluate the long-term effects of Adderall, or other amphetamine compounds, in the treatment of adults with ADHD.
AB - Background: We report on a controlled trial of a mixed amphetamine salts compound (Adderall, dextroamphetamine sulfate, dextro-, levoamphetamine sulfate, dextroamphetamine aspartate, levoamphetamine aspartate, and dextroamphetamine saccharate) in the treatment of adult attention-deficit/hyperactivity disorder (ADHD). Methods: This was a 7-week, randomized, double-blind, placebo-controlled, crossover study of Adderall in 27 well-characterized adults satisfying full DSM-IV criteria for ADHD of childhood onset and persistent symptoms into adulthood. Medication was titrated up to 30 mg twice a day. Outcome measures included the ADHD Rating Scale and the Clinical Global Impression Score. Comorbid psychiatric disorders were assessed to test for potential effects on treatment outcome. Results: Treatment with Adderall at an average oral dose of 54 mg (administered in 2 daily doses) was effective and well tolerated. Drug-specific improvement in ADHD symptoms was highly significant overall (42% decrease on the ADHD Rating Scale, P<.001), and sufficiently robust to be detectable in a parallel groups comparison restricted to the first 3 weeks of the protocol (P<.001). The percentage of subjects who improved (reduction in the ADHD rating scale of ≥30%) was significantly higher with Adderall treatment than with a placebo (70% vs 7%; P=.001). Conclusions: Adderall was effective and well tolerated in the short-term treatment of adults with ADHD. More work is needed to evaluate the long-term effects of Adderall, or other amphetamine compounds, in the treatment of adults with ADHD.
UR - http://www.scopus.com/inward/record.url?scp=0034888151&partnerID=8YFLogxK
U2 - 10.1001/archpsyc.58.8.775
DO - 10.1001/archpsyc.58.8.775
M3 - Article
C2 - 11483144
AN - SCOPUS:0034888151
SN - 0003-990X
VL - 58
SP - 775
EP - 782
JO - Archives of General Psychiatry
JF - Archives of General Psychiatry
IS - 8
ER -