首页> 外文期刊>Journal of clinical psychopharmacology >A double-blind placebo-controlled trial of bupropion sustained-release for smoking cessation in schizophrenia.
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A double-blind placebo-controlled trial of bupropion sustained-release for smoking cessation in schizophrenia.

机译:安非他酮缓释用于精神分裂症戒烟的双盲安慰剂对照试验。

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摘要

The objective of this study was to examine the efficacy of bupropion for smoking cessation in patients with schizophrenia. Adults with schizophrenia who smoked more than 10 cigarettes per day and wished to try to quit smoking were recruited from community mental health centers, enrolled in a 12-week group cognitive behavioral therapy intervention, and randomly assigned to receive either bupropion sustained-release 300 mg/d or identical placebo. Fifty-three adults, 25 on bupropion and 28 on placebo, were randomized, completed at least 1 postbaseline assessment and were included in the analysis. The primary outcome measures were 7-day point prevalence abstinence in the week after the quit date (week 4) and at the end of the intervention (week 12). Subjects in the bupropion group were significantly more likely to be abstinent for the week after the quit date (36% [9/25] vs. 7% [2/28], P = 0.016) and at end of the intervention (16% [4/25] vs. 0%, P = 0.043). Subjects in the bupropion group also had a higher rate of 4-week continuous abstinence (weeks 8-12) (16% [4/25] vs. 0%, P = 0.043) and a longer duration of abstinence (4.2 [3.2] weeks vs. 1.8 [0.96] weeks, t = 2.30, P = 0.037). The effect of bupropion did not persist after discontinuation of treatment. Subjects in the bupropion group had no worsening of clinical symptoms and had a trend toward improvement in depressive and negative symptoms. We conclude that bupropion does not worsen clinical symptoms of schizophrenia and is modestly effective for smoking cessation in patients with schizophrenia. The relapse rate is high after treatment discontinuation.
机译:这项研究的目的是检查安非他酮对精神分裂症患者戒烟的功效。从社区精神卫生中心招募了每天抽烟超过10支并希望戒烟的精神分裂症成年人,参加了为期12周的集体认知行为疗法干预,并随机分配接受安非他酮缓释300 mg / d或相同的安慰剂。将53名成人(安非他酮治疗组25名,安慰剂治疗组28名)随机分组,至少完成1次基线后评估,并将其纳入分析。主要结局指标为戒烟日期后第一周(第4周)和干预结束时(第12周)的7天戒断率。安非他酮组的受试者戒断后一周内禁欲的可能性明显更高(36%[9/25] vs. 7%[2/28],P = 0.016)和干预结束时(16%) [4/25] vs. 0%,P = 0.043)。安非他酮组的受试者连续4周禁欲的发生率较高(第8-12周)(16%[4/25] vs. 0%,P = 0.043),禁欲持续时间较长(4.2 [3.2]周vs. 1.8 [0.96]周,t = 2.30,P = 0.037)。在停止治疗后安非他酮的作用没有持续。安非他酮组的受试者临床症状无恶化,抑郁和阴性症状均有改善的趋势。我们得出的结论是,安非他酮不会使精神分裂症的临床症状恶化,并且对于精神分裂症患者的戒烟是适度有效的。停药后复发率很高。

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