Gourlay S G, Stead L F, Benowitz N L
16 Manning Street, Queens Park, Australia, NSW 2022.
Cochrane Database Syst Rev. 2004;2004(3):CD000058. doi: 10.1002/14651858.CD000058.pub2.
Clonidine was originally used to lower blood pressure. It acts on the central nervous system and may reduce withdrawal symptoms in various addictive behaviours, including tobacco use.
The aim of this review is to determine clonidine's effectiveness in helping smokers to quit.
We searched the Cochrane Tobacco Addiction Group trials register for trials of clonidine. Date of the most recent search: May 2004.
We considered randomized trials of clonidine versus placebo with a smoking cessation endpoint assessed at least 12 weeks following the end of treatment.
We extracted data in duplicate on the type of subjects, the dose and duration of clonidine therapy, the outcome measures, method of randomization, and completeness of follow up. The main outcome measure was abstinence from smoking after at least 12 weeks follow up in patients smoking at baseline. We used the most rigorous definition of abstinence for each trial, and biochemically validated rates if available. Where appropriate, we performed meta-analysis using a fixed effect model.
Six trials met the inclusion criteria. There were three trials of oral, and three of transdermal clonidine. Some form of behavioural counselling was offered to all participants in five of the six trials. There was a statistically significant effect of clonidine in one of these trials. The pooled odds ratio for success with clonidine versus placebo was 1.89 (95% confidence interval 1.30 to 2.74). There was a high incidence of dose-dependent side-effects, particularly dry mouth and sedation.
REVIEWERS' CONCLUSIONS: Based on a small number of trials, in which there are potential sources of bias, clonidine is effective in promoting smoking cessation. Prominent side-effects limit the usefulness of clonidine for smoking cessation.
可乐定最初用于降低血压。它作用于中枢神经系统,可能减轻包括烟草使用在内的各种成瘾行为的戒断症状。
本综述的目的是确定可乐定在帮助吸烟者戒烟方面的有效性。
我们检索了Cochrane烟草成瘾小组试验注册库中有关可乐定的试验。最近一次检索日期:2004年5月。
我们纳入了可乐定与安慰剂对照的随机试验,治疗结束后至少12周评估戒烟终点。
我们对受试者类型、可乐定治疗的剂量和疗程、结局指标、随机化方法以及随访完整性进行了双人数据提取。主要结局指标是基线吸烟的患者在至少12周随访后戒烟。我们对每个试验采用最严格的戒烟定义,如有可用则采用生化验证率。在适当情况下,我们使用固定效应模型进行荟萃分析。
六项试验符合纳入标准。三项为口服可乐定试验,三项为透皮可乐定试验。六项试验中的五项为所有参与者提供了某种形式的行为咨询。其中一项试验中可乐定有统计学显著效果。可乐定与安慰剂相比成功的合并比值比为1.89(95%置信区间1.30至2.74)。剂量依赖性副作用发生率高,尤其是口干和镇静。
基于少数存在潜在偏倚来源的试验,可乐定在促进戒烟方面有效。显著的副作用限制了可乐定用于戒烟的效用。