Chakrabarti A, Bagnall A, Chue P, Fenton M, Palaniswamy V, Wong W, Xia J
Malham House, Hyde Terrace, Leeds, UK.
Cochrane Database Syst Rev. 2007 Oct 17;2007(4):CD001943. doi: 10.1002/14651858.CD001943.pub2.
Some authors have suggested that loxapine is more effective than typical antipsychotics in reducing the negative symptoms of schizophrenia, that extrapyramidal adverse effects are not usually seen at clinically effective antipsychotic doses and that it should therefore be classed as atypical.
To determine the effects of loxapine compared with placebo, typical and other atypical antipsychotic drugs for schizophrenia and related psychoses.
For this 2007 update, we searched the Cochrane Schizophrenia Group's Register (January 2007).
We included all randomised controlled clinical trials relevant to the care of schizophrenia that compared loxapine to other treatments.
We independently inspected abstracts ordered papers, re-inspected and quality assessed these. 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 numbers needed to treat/harm (NNT/NNH) where appropriate. For continuous data, we calculated weighted mean differences (WMD) again based on a fixed effects model.
We were able to include 41 studies in this review. Compared with placebo, loxapine has an antipsychotic effect (Global effect - not improved at six weeks: n=78, 2 RCTs, RR 0.30 CI 0.1 to 0.6 NNT 3 CI 3 to 5). It is as effective as typical drugs in the short term (4 -12 weeks) (Global effect: n=580, 13 RCTs, RR 0.86 CI 0.7 to 1.1; mental state: n=915, 6 RCTs, RR 0.89 CI 0.8 to 1.1). Very limited heterogeneous data suggest that, given intramuscularly (IM), loxapine may be at least as sedating as IM haloperidol and thiothixene. Loxapine is also as effective as atypicals (risperidone, quetiapine) (n=468, 6 RCTs, RR mental state not improved 1.07 CI 0.8 to 1.5). Adverse effect profile is similar to typicals but loxapine may cause more extrapyramidal adverse effects when compared with atypicals (n=340, 4 RCTs, RR 2.18 CI 1.6 to 3.1).
AUTHORS' CONCLUSIONS: Loxapine is an antipsychotic which is not clearly distinct from typical or atypical drugs in terms of its effects on global or mental state. Loxapines profile of adverse effects is similar to that of the older generation of antipsychotic drugs.
一些作者认为洛沙平在减轻精神分裂症阴性症状方面比传统抗精神病药物更有效,在临床有效的抗精神病药物剂量下通常不会出现锥体外系不良反应,因此应归类为非典型抗精神病药物。
确定洛沙平与安慰剂、传统及其他非典型抗精神病药物相比,对精神分裂症及相关精神病的疗效。
为进行2007年的更新,我们检索了Cochrane精神分裂症研究组注册库(2007年1月)。
我们纳入了所有与精神分裂症治疗相关的随机对照临床试验,这些试验比较了洛沙平与其他治疗方法。
我们独立检查了订购论文的摘要,再次检查并进行质量评估。对于二分数据,我们基于固定效应模型在意向性分析的基础上计算相对风险(RR)及其95%置信区间(CI)。在适当的情况下,我们计算了治疗所需人数/伤害所需人数(NNT/NNH)。对于连续性数据,我们同样基于固定效应模型计算加权平均差(WMD)。
我们能够在本综述中纳入41项研究。与安慰剂相比,洛沙平具有抗精神病作用(整体疗效 - 六周时未改善:n = 78,2项随机对照试验,RR 0.30,CI 0.1至0.6,NNT 3,CI 3至5)。在短期(4 - 12周)内,它与传统药物一样有效(整体疗效:n = 580,13项随机对照试验,RR 0.86 CI 0.7至1.1;精神状态:n = 915,6项随机对照试验,RR 0.89 CI 0.8至1.1)。非常有限的异质性数据表明,肌肉注射洛沙平的镇静作用可能至少与肌肉注射氟哌啶醇和硫利达嗪一样强。洛沙平与非典型药物(利培酮、喹硫平)同样有效(n = 468,6项随机对照试验;精神状态未改善的RR为1.07,CI 0.8至1.5)。不良反应谱与传统药物相似,但与非典型药物相比,洛沙平可能导致更多的锥体外系不良反应(n = 340,4项随机对照试验,RR 2.18 CI 1.6至3.1)。
就对整体或精神状态的影响而言,洛沙平作为一种抗精神病药物,与传统或非典型药物并无明显区别。洛沙平的不良反应谱与 older generation of antipsychotic drugs(此处原文有误,推测应为“老一代抗精神病药物”)相似。