Tsoi Daniel T, Porwal Mamta, Webster Angela C
Nottinghamshire Healthcare NHS Trust, Nottingham, UK.
Cochrane Database Syst Rev. 2013 Feb 28;2013(2):CD007253. doi: 10.1002/14651858.CD007253.pub3.
Individuals with schizophrenia smoke more heavily than the general population and this contributes to their higher morbidity and mortality from smoking-related illnesses. It remains unclear what interventions can help them to quit or to reduce smoking.
To evaluate the benefits and harms of different treatments for nicotine dependence in schizophrenia.
We searched electronic databases including MEDLINE, EMBASE and PsycINFO from inception to October 2012, and the Cochrane Tobacco Addiction Group Specialized Register in November 2012.
We included randomised trials for smoking cessation or reduction, comparing any pharmacological or non-pharmacological intervention with placebo or with another therapeutic control in adult smokers with schizophrenia or schizoaffective disorder.
Two reviewers independently assessed the eligibility and quality of trials, as well as extracted data. Outcome measures included smoking abstinence, reduction in the amount smoked and any change in mental state. We extracted abstinence and reduction data at the end of treatment and at least six months after the intervention. We used the most rigorous definition of abstinence or reduction and biochemically validated data where available. We noted any reported adverse events. Where appropriate, we pooled data using a random-effects model.
We included 34 trials (16 trials of cessation; nine trials of reduction; one trial of relapse prevention; eight trials that reported smoking outcomes for interventions aimed at other purposes). Seven trials compared bupropion with placebo; meta-analysis showed that cessation rates after bupropion were significantly higher than placebo at the end of treatment (seven trials, N = 340; risk ratio [RR] 3.03; 95% confidence interval [CI] 1.69 to 5.42) and after six months (five trials, N = 214, RR 2.78; 95% CI 1.02 to 7.58). There were no significant differences in positive, negative and depressive symptoms between bupropion and placebo groups. There were no reports of major adverse events such as seizures with bupropion.Smoking cessation rates after varenicline were significantly higher than placebo, at the end of treatment (2 trials, N = 137; RR 4.74, 95% CI 1.34 to 16.71). Only one trial reported follow-up at six months and the CIs were too wide to provide evidence of a sustained effect (one trial, N = 128, RR 5.06, 95% CI 0.67 to 38.24). There were no significant differences in psychiatric symptoms between the varenicline and placebo groups. Nevertheless, there were reports of suicidal ideation and behaviours from two people on varenicline.Two studies reported that contingent reinforcement (CR) with money may increase smoking abstinence rates and reduce the level of smoking in patients with schizophrenia. However, it is uncertain whether these benefits can be maintained in the longer term. There was no evidence of benefit for the few trials of other pharmacological therapies (including nicotine replacement therapy (NRT)) and psychosocial interventions in helping smokers with schizophrenia to quit or reduce smoking.
AUTHORS' CONCLUSIONS: Bupropion increases smoking abstinence rates in smokers with schizophrenia, without jeopardizing their mental state. Varenicline may also improve smoking cessation rates in schizophrenia, but its possible psychiatric adverse effects cannot be ruled out. CR may help this group of patients to quit and reduce smoking in the short term. We failed to find convincing evidence that other interventions have a beneficial effect on smoking in schizophrenia.
精神分裂症患者吸烟比普通人群更为严重,这导致他们因吸烟相关疾病而出现更高的发病率和死亡率。目前尚不清楚哪些干预措施可以帮助他们戒烟或减少吸烟。
评估针对精神分裂症患者尼古丁依赖的不同治疗方法的益处和危害。
我们检索了电子数据库,包括自数据库建立至2012年10月的MEDLINE、EMBASE和PsycINFO,以及2012年11月的Cochrane烟草成瘾小组专业注册库。
我们纳入了关于戒烟或减少吸烟的随机试验,比较了任何药物或非药物干预与安慰剂或与精神分裂症或分裂情感性障碍成年吸烟者的另一种治疗对照。
两名评价员独立评估试验的合格性和质量,并提取数据。结局指标包括戒烟、吸烟量减少以及精神状态的任何变化。我们在治疗结束时以及干预后至少六个月提取戒烟和减少吸烟的数据。我们采用最严格的戒烟或减少吸烟定义,并在可行时采用经生化验证的数据。我们记录了所有报告的不良事件。在适当情况下,我们使用随机效应模型合并数据。
我们纳入了34项试验(16项戒烟试验;9项减少吸烟试验;1项预防复发试验;8项报告了针对其他目的干预措施的吸烟结局试验)。7项试验比较了安非他酮与安慰剂;荟萃分析表明,在治疗结束时(7项试验,N = 340;风险比[RR] 3.03;95%置信区间[CI] 1.69至5.42)以及六个月后(5项试验,N = 214,RR 2.78;95% CI 1.02至7.58),安非他酮治疗后的戒烟率显著高于安慰剂。安非他酮组与安慰剂组在阳性、阴性和抑郁症状方面无显著差异。没有关于安非他酮引起癫痫等重大不良事件的报告。在治疗结束时,伐尼克兰治疗后的戒烟率显著高于安慰剂(2项试验,N = 137;RR 4.74,95% CI 1.34至16.71)。只有1项试验报告了六个月的随访情况,其置信区间过宽,无法提供持续效果的证据(1项试验,N = 128,RR 5.06,95% CI 0.67至38.24)。伐尼克兰组与安慰剂组在精神症状方面无显著差异。然而,有两名服用伐尼克兰的患者报告了自杀意念和行为。两项研究报告称,金钱奖励强化(CR)可能会提高精神分裂症患者的戒烟率并降低吸烟水平。然而,这些益处能否长期维持尚不确定。对于其他药物治疗(包括尼古丁替代疗法(NRT))和心理社会干预的少数试验,没有证据表明它们有助于精神分裂症吸烟者戒烟或减少吸烟。
安非他酮可提高精神分裂症吸烟者的戒烟率,且不危及他们的精神状态。伐尼克兰也可能提高精神分裂症患者的戒烟率,但不能排除其可能的精神方面不良反应。金钱奖励强化可能有助于这组患者在短期内戒烟和减少吸烟。我们未能找到令人信服的证据表明其他干预措施对精神分裂症患者的吸烟有有益影响。