A pilot study of lis-dexamfetamine dimesylate (LDX/SPD489) to facilitate smoking cessation in nicotine-dependent adults with ADHD
- PMID: 22508760
- PMCID: PMC3421044
- DOI: 10.1177/1087054712440320
A pilot study of lis-dexamfetamine dimesylate (LDX/SPD489) to facilitate smoking cessation in nicotine-dependent adults with ADHD
Abstract
Objective: The goal of this study was to assess the efficacy and tolerability of lis-dexamfetamine dimesylate (LDX) as an adjunct to nicotine replacement therapy in adult smokers with ADHD who were undergoing a quit attempt.
Methods: Thirty-two regular adult smokers with ADHD were randomized to receive LDX (n = 17) or placebo (n = 15) in addition to nicotine patch concurrent with a quit attempt.
Results: There were no differences between smokers assigned to LDX versus placebo in any smoking outcomes. Participants treated with LDX demonstrated significant reductions in self-reported and clinician-rated ADHD symptoms. LDX was well tolerated in smokers attempting to quit.
Discussion: In general, LDX does not facilitate smoking cessation in adults with ADHD more than does placebo, though both groups significantly reduced smoking. LDX demonstrated efficacy for reducing ADHD symptoms in adult smokers engaging in a quit attempt.
Keywords: adult ADHD; lis-dexamfetamine dimesylate; smoking.
Conflict of interest statement
The authors declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: During the period of the study, the following disclosures are noted. Dr. Kollins received research support and/or consulting fees fro, Shire Pharmaceuticals, Otsuka Pharmaceuticals, Addrenex Pharmaceuticals, Pfizer Inc., and NIDA/NIH. Dr. McClernon received research support from Philip Morris USA and NIDA/NIH. The other authors have nothing to disclose.
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