Rathbone John, Variend Hannele, Mehta Hetal
Cochrane Schizophrenia Group, University of Nottingham, Duncan MacMillan House, Portchester Road, Nottingham, UK, NG3 6AA.
Cochrane Database Syst Rev. 2008 Jul 16(3):CD004837. doi: 10.1002/14651858.CD004837.pub2.
Many people with schizophrenia use cannabis and its effects on the illness are unclear.
To evaluate the effects of cannabis use on people with schizophrenia and schizophrenia-like illnesses.
We searched the Cochrane Schizophrenia Group Trials Register (April 2007) which is based on regular searches of BIOSIS, CENTRAL, CINAHL, EMBASE, MEDLINE and PsycINFO.
We included all randomised trials involving cannabinoids and people with schizophrenia or schizophrenia-like illnesses.
We extracted data independently. For dichotomous data we calculated relative risks (RR) and their 95% confidence intervals (CI) on an intention-to-treat basis, based on a fixed effects model. We calculated the numbers needed to treat/harm (NNT/NNH). For continuous data, we calculated weighted mean differences (WMD) again based on a fixed effects model.
We identified one randomised trial. No significant differences were found between the Cannabis and Psychosis Therapy (CAP) intervention group and the Psychoeducaton (PE) intervention for use of cannabis at three months assessment (n=47, RR 1.04 CI 0.6 to 1.7). BPRS-extended scale scores at three months assessment (n=47, WMD -3.60 CI -12.8 to 5.6) and nine months assessment (n=47, WMD 0.80 CI -7.5 to 9.1) were non-significant between CAP and PE. We found no significant improvement in social functioning in the CAP group compared with PE (at 3 months, n=47, WMD -0.80 CI -10 to 8.4) and (at 9 months, n=47, WMD -4.70 CI -14.5 to 5.1).
AUTHORS' CONCLUSIONS: At present, there is insufficient evidence to support or refute the use of cannabis/cannabinoid compounds for people suffering with schizophrenia. This review highlights the need for well designed, conducted and reported clinical trials to address the potential effects of cannabis based compounds for people with schizophrenia.
许多精神分裂症患者使用大麻,但其对病情的影响尚不清楚。
评估使用大麻对精神分裂症患者及类精神分裂症疾病患者的影响。
我们检索了Cochrane精神分裂症研究组试验注册库(2007年4月),该注册库基于对BIOSIS、CENTRAL、CINAHL、EMBASE、MEDLINE和PsycINFO的定期检索。
我们纳入了所有涉及大麻素与精神分裂症患者或类精神分裂症疾病患者的随机试验。
我们独立提取数据。对于二分数据,我们基于意向性分析,采用固定效应模型计算相对风险(RR)及其95%置信区间(CI)。我们计算了治疗所需人数/伤害所需人数(NNT/NNH)。对于连续数据,我们同样基于固定效应模型计算加权平均差(WMD)。
我们识别出一项随机试验。在三个月评估时,大麻与精神病治疗(CAP)干预组和心理教育(PE)干预组在大麻使用方面未发现显著差异(n = 47,RR 1.04,CI 0.6至1.7)。在三个月评估时(n = 47,WMD -3.60,CI -12.8至5.6)和九个月评估时(n = 47,WMD 0.80,CI -7.5至9.1),CAP组和PE组在BPRS扩展量表评分上无显著差异。与PE组相比,我们发现CAP组在社会功能方面没有显著改善(三个月时,n = 47,WMD -0.80,CI -10至8.4)以及(九个月时,n = 47,WMD -4.70,CI -14.5至5.)。
目前,没有足够的证据支持或反驳精神分裂症患者使用大麻/大麻素化合物。本综述强调需要进行设计良好、实施规范且报告完整的临床试验,以研究大麻类化合物对精神分裂症患者的潜在影响。