A Contingency-Management Intervention to Promote Initial Smoking Cessation Among Opioid-Maintained Patients

被引:61
|
作者
Dunn, Kelly E. [4 ]
Sigmon, Stacey C. [1 ,2 ]
Reimann, Edward F. [1 ]
Badger, Gary J. [3 ]
Heil, Sarah H. [1 ,2 ]
Higgins, Stephen T. [1 ,2 ]
机构
[1] Univ Vermont, Dept Psychiat, Burlington, VT 05401 USA
[2] Univ Vermont, Dept Psychol, Burlington, VT 05401 USA
[3] Univ Vermont, Dept Med Biostat, Burlington, VT 05401 USA
[4] Johns Hopkins Univ, Sch Med, Dept Psychiat, Baltimore, MD 21218 USA
关键词
contingency management; smoking cessation; methadone; buprenorphine; bupropion; VOUCHER-BASED INCENTIVES; SUSTAINED-RELEASE BUPROPION; RECEPTOR PARTIAL AGONIST; CIGARETTE-SMOKING; NICOTINE DEPENDENCE; SUBSTANCE-ABUSE; TOBACCO USE; METHADONE; ABSTINENCE; REINFORCEMENT;
D O I
10.1037/a0018649
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Prevalence of cigarette smoking among opioid-maintained patients is more than threefold that of the general population and associated with increased morbidity and mortality. Relatively few studies have evaluated smoking interventions in this population. The purpose of the present study was to examine the efficacy of contingency management for promoting initial smoking abstinence. Forty methadone- or buprenorphine-maintained cigarette smokers were randomly assigned to a contingent (n = 20) or noncontingent (n = 20) experimental group and visited the clinic for 14 consecutive days. Contingent participants received vouchers based on breath carbon monoxide levels during Study Days 1 to 5 and urinary cotinine levels during Days 6 to 14. Voucher earnings began at $9.00 and increased by $1.50 with each subsequent negative sample for maximum possible of $362.50. Noncontingent participants earned vouchers independent of smoking status. Although not a primary focus, participants who were interested and medically eligible could also receive bupropion (Zyban). Contingent participants achieved significantly more initial smoking abstinence, as evidenced by a greater percentage of smoking-negative samples (55% vs. 17%) and longer duration of continuous abstinence (7.7 vs. 2.4 days) during the 2 week quit attempt than noncontingent participants, respectively. Bupropion did not significantly influence abstinence outcomes. Results from this randomized clinical trial support the efficacy of contingency management interventions in promoting initial smoking abstinence in this challenging population.
引用
收藏
页码:37 / 50
页数:14
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