Hajek P, Stead L F
Department of Human Science and Medical Ethics, St Bartholomew's and the Royal London School of Medicine and Dentistry, Turner Street, London, UK, E1 2AD.
Cochrane Database Syst Rev. 2004;2001(3):CD000546. doi: 10.1002/14651858.CD000546.pub2.
Aversion therapy pairs the pleasurable stimulus of smoking a cigarette with some unpleasant stimulus. The objective is to extinguish the urge to smoke.
This review has two aims: First, to determine the efficacy of rapid smoking and other aversive methods in helping smokers to stop smoking; Second, to determine whether there is a dose-response effect on smoking cessation at different levels of aversive stimulation.
We searched the Cochrane Tobacco Addiction Group trials register for studies which evaluated any technique of aversive smoking.
Randomized trials which compared aversion treatments with 'inactive' procedures or which compared aversion treatments of different intensity for smoking cessation. Trials must have reported follow up of least six months from beginning of treatment.
We extracted data in duplicate on the study population, the type of aversion treatment, the outcome measure, method of randomization and completeness of follow up. The outcome measure was abstinence from smoking at maximum follow up, using the strictest measure reported by the authors. Subjects lost to follow up were regarded as smokers. Where appropriate, we performed meta-analysis using a fixed effect model.
Twenty-five trials met the inclusion criteria. Twelve included rapid smoking and nine used other aversion methods. Ten trials included two or more conditions allowing assessment of a dose-response to aversive stimulation. The odds ratio (OR) for abstinence following rapid smoking compared to control was 1.98 (95% confidence intervals (CI): 1.36 to 2.90). Several factors suggest that this finding should be interpreted cautiously. A funnel plot of included studies was asymmetric, due to the relative absence of small studies with negative results. Most trials had a number of serious methodological problems likely to lead to spurious positive results. The only trial using biochemical validation of all self reported cessation gave a non-significant result. Other aversion methods were not shown to be effective (odds ratio 1.15, 95% confidence interval 0.73 to 1.82). There was a borderline dose-response to the level of aversive stimulation (OR 1.66, 95% CI: 1.00 to 2.78).
REVIEWERS' CONCLUSIONS: The existing studies provide insufficient evidence to determine the efficacy of rapid smoking, or whether there is a dose-response to aversive stimulation. Milder versions of aversive smoking seem to lack specific efficacy. Rapid smoking is an unproven method with sufficient indications of promise to warrant evaluation using modern rigorous methodology.
厌恶疗法将吸烟带来的愉悦刺激与某种不愉快刺激配对。目的是消除吸烟冲动。
本综述有两个目标:第一,确定快速吸烟及其他厌恶方法在帮助吸烟者戒烟方面的疗效;第二,确定在不同程度的厌恶刺激下,戒烟是否存在剂量反应效应。
我们检索了Cochrane烟草成瘾小组试验注册库,以查找评估任何厌恶吸烟技术的研究。
将厌恶疗法与“无活性”程序进行比较,或比较不同强度厌恶疗法对戒烟效果的随机试验。试验必须报告从治疗开始至少六个月的随访情况。
我们对研究人群、厌恶治疗类型、结局指标、随机化方法和随访完整性进行了双人数据提取。结局指标是在最长随访期时戒烟情况,采用作者报告的最严格标准。失访受试者视为吸烟者。在适当情况下,我们使用固定效应模型进行荟萃分析。
25项试验符合纳入标准。12项试验采用快速吸烟法,9项试验采用其他厌恶方法。10项试验包含两种或更多条件,可用于评估对厌恶刺激的剂量反应。与对照组相比,快速吸烟后戒烟的比值比(OR)为1.98(95%置信区间(CI):1.36至2.90)。有几个因素表明,这一结果应谨慎解读。纳入研究的漏斗图不对称,因为相对缺乏结果为阴性的小型研究。大多数试验存在一些严重的方法学问题,可能导致虚假的阳性结果。唯一一项对所有自我报告戒烟情况进行生化验证的试验结果无统计学意义。其他厌恶方法未显示有效(比值比1.15,95%置信区间0.73至1.82)。对厌恶刺激水平存在临界剂量反应(OR 1.66,95% CI:1.00至2.78)。
现有研究提供的证据不足,无法确定快速吸烟的疗效,也无法确定是否存在对厌恶刺激的剂量反应。较温和的厌恶吸烟方法似乎缺乏特异性疗效。快速吸烟是一种未经证实的方法,但有足够迹象表明有前景,值得使用现代严格方法进行评估。