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  • A randomized trial of concurrent smoking-cessation and substance use disorder treatment in stimulant-dependent smokers.

A randomized trial of concurrent smoking-cessation and substance use disorder treatment in stimulant-dependent smokers.

The Journal of clinical psychiatry (2013-12-19)
Theresa M Winhusen, Gregory S Brigham, Frankie Kropp, Robert Lindblad, John G Gardin, Pat Penn, Candace Hodgkins, Thomas M Kelly, Antoine Douaihy, Michael McCann, Lee D Love, Eliot DeGravelles, Ken Bachrach, Susan C Sonne, Bob Hiott, Louise Haynes, Gaurav Sharma, Daniel F Lewis, Paul VanVeldhuisen, Jeff Theobald, Udi Ghitza
ABSTRACT

To evaluate the impact of concurrent treatments for substance use disorder and nicotine-dependence for stimulant-dependent patients. A randomized, 10-week trial with follow-up at 3 and 6 months after smoking quit date conducted at 12 substance use disorder treatment programs between February 2010 and July 2012. Adults meeting DSM-IV-TR criteria for cocaine and/or methamphetamine dependence and interested in quitting smoking were randomized to treatment as usual (n = 271) or treatment as usual with smoking-cessation treatment (n = 267). All participants received treatment as usual for substance use disorder treatment. Participants assigned to treatment as usual with concurrent smoking-cessation treatment received weekly individual smoking cessation counseling and extended-release bupropion (300 mg/d) during weeks 1-10. During post-quit treatment (weeks 4-10), participants assigned to treatment as usual with smoking-cessation treatment received a nicotine inhaler and contingency management for smoking abstinence. Weekly proportion of stimulant-abstinent participants during the treatment phase, as assessed by urine drug screens and self-report, was the primary outcome. Secondary measures included other substance/nicotine use outcomes and treatment attendance. There were no significant treatment effects on stimulant-use outcomes, as measured by the primary outcome and stimulant-free days, on drug-abstinence, or on attendance. Participants assigned to treatment as usual with smoking-cessation treatment, relative to those assigned to treatment as usual, had significantly better outcomes for drug-free days at 6-month follow-up (χ(2)(1) = 4.09, P <.05), with a decrease in drug-free days from baseline of -1.3% in treatment as usual with smoking-cessation treatment and of -7.6% in treatment as usual. Participants receiving treatment as usual with smoking-cessation treatment, relative to those receiving treatment as usual, had significantly better outcomes on smoking point-prevalence abstinence (25.5% vs 2.2%; χ(2)(1) = 44.69, P < .001; OR =18.2). These results suggest that providing smoking-cessation treatment to illicit stimulant-dependent patients in outpatient substance use disorder treatment will not worsen, and may enhance, abstinence from nonnicotine substance use. ClinicalTrials.gov identifier: NCT01077024.

MATERIALS
Product Number
Brand
Product Description

USP
Bupropion hydrochloride, United States Pharmacopeia (USP) Reference Standard
Sigma-Aldrich
Bupropion hydrochloride, ≥98% (HPLC), solid
Supelco
Bupropion hydrochloride solution, 1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®