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Bupropion and Naltrexone for Smoking Cessation: A Double-Blind Randomized Placebo-Controlled Clinical Trial

机译:安非他酮和纳曲酮用于戒烟的双盲随机安慰剂对照临床试验

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摘要

Combination of non-nicotine pharmacotherapies has been under-examined for cigarette smoking cessation. A randomized, double-blind, parallel-group double-dummy study evaluated two medications, bupropion (BUP) and naltrexone (NTX), in treatment-seeking cigarette smokers (N = 121) over a 7-week treatment intervention with 6-month follow-up. Smokers were randomized to either BUP (300 mg/day) + Placebo (PBO) or BUP (300 mg/day) + NTX (50 mg/day). The primary outcome was biochemically-verified (saliva cotinine, carbon monoxide) 7-day, point-prevalence abstinence. BUP+NTX was associated with significantly higher point-prevalence abstinence rates after 7-weeks of treatment (BUP+NTX, 54.1%; BUP+PBO, 33.3%), p = 0.0210, but not at 6-month follow-up (BUP+NTX, 27.9%; BUP+PBO, 15.0%), p = 0.09. Continuous abstinence rates did not differ, p = 0.0740 (BUP+NTX, 26.2%; BUP+PBO, 13.3%). Those receiving BUP+NTX reported reduced nicotine withdrawal, p = 0.0364. The BUP+NTX combination was associated with elevated rates of some side effects, but with no significant difference in retention between the groups.
机译:对于戒烟,非尼古丁药物治疗的组合已被检查不足。一项随机,双盲,平行组双模拟研究评估了寻求治疗的吸烟者(N = 121)中的安非他酮(BUP)和纳曲酮(NTX)这两种药物,历时7周,治疗6个月。跟进。吸烟者随机分为BUP(300 mg /天)+安慰剂(PBO)或BUP(300 mg /天)+ NTX(50 mg /天)。主要结局是经过7天生化检查(唾液可替宁,一氧化碳),点流行戒断。 BUP + NTX与治疗7周后的更高的点流行率(BUP + NTX,54.1%; BUP + PBO,33.3%)相关,p = 0.0210,但在6个月的随访中没有+ NTX,27.9%; BUP + PBO,15.0%),p = 0.09。持续戒酒率没有差异,p = 0.0740(BUP + NTX,26.2%; BUP + PBO,13.3%)。那些接受BUP + NTX治疗的患者报告尼古丁戒断减少,p = 0.0364。 BUP + NTX组合与某些副作用发生率升高相关,但两组之间的保留率无显着差异。

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