Department of Psychiatry and Psychotherapy, Technical University Munich, Ismaninger Straße 22, 81675 Munich, Germany.
Eur Neuropsychopharmacol. 2013 Sep;23(9):1023-33. doi: 10.1016/j.euroneuro.2013.03.001. Epub 2013 Apr 17.
Applying various psychopharmacological combination and augmentation strategies in schizophrenia is common clinical practice. This meta-analysis evaluated the efficacy of benzodiazepines added to antipsychotics. The Cochrane Schizophrenia Group trial register (until February 2011) and PubMed/Medline (until July 2012) were searched for randomized controlled trials (RCTs) with a minimum duration of one week that compared benzodiazepine augmentation of antipsychotics with a control group receiving antipsychotic monotherapy in schizophrenia and schizophrenia-like psychoses. Study selection and data extraction were conducted independently by at least two authors. The primary outcome was response to treatment. Secondary outcomes were positive and negative schizophrenic symptoms, anxiety symptoms, and dropouts due to any reason, inefficacy of treatment, and adverse events. Pooled risk ratios (RRs) with the 95% confidence intervals (CIs) were calculated using a random-effects model, with number-needed-to-treat/harm (NNT/H) calculations where appropriate. Overall, 16 relevant RCTs with 1045 participants were identified. Benzodiazepine augmentation was not associated with statistically significantly more responders (N=6; n=511; RR 0.97, 95% CI 0.77-1.22). Adjunctive benzodiazepines were well accepted and tolerated according to dropout-rates and adverse effects apart from dizziness (N=3; n=190; RR 2.58, 95% CI 1.08-6.15) and somnolence (N=2; n=118; RR 3.30, 95% CI 1.04-10.40). There is no evidence for antipsychotic efficacy of additional benzodiazepine medication in schizophrenia. Therefore, benzodiazepines should be considered primarily for desired ultra short-term sedation of acutely agitated patients but not for augmentation of antipsychotics in the medium- and long-term pharmacotherapy of schizophrenia and related disorders.
在精神分裂症中应用各种精神药理学的联合和增强策略是常见的临床实践。本荟萃分析评估了苯二氮䓬类药物联合抗精神病药物的疗效。对 Cochrane 精神分裂症组试验注册库(截至 2011 年 2 月)和 PubMed/Medline(截至 2012 年 7 月)进行检索,纳入比较苯二氮䓬类药物增强抗精神病药物与接受抗精神病药物单药治疗的精神分裂症和类似精神分裂症的精神障碍患者的随机对照试验(RCT),疗程至少 1 周。至少由两位作者独立进行研究选择和数据提取。主要结局是治疗反应。次要结局是阳性和阴性精神分裂症症状、焦虑症状、任何原因导致的脱落、治疗无效和不良事件。采用随机效应模型计算合并风险比(RR)及其 95%置信区间(CI),并适当计算需要治疗的人数/危害(NNT/H)。总体上,纳入了 16 项包含 1045 名参与者的相关 RCT。苯二氮䓬类药物增强治疗与应答者的数量无统计学显著差异(N=6;n=511;RR 0.97,95%CI 0.77-1.22)。根据脱落率和不良反应(除头晕外,N=3;n=190;RR 2.58,95%CI 1.08-6.15)和嗜睡(N=2;n=118;RR 3.30,95%CI 1.04-10.40),苯二氮䓬类药物辅助治疗具有良好的可接受性和耐受性。精神分裂症中,没有证据表明额外的苯二氮䓬类药物治疗具有抗精神病作用。因此,苯二氮䓬类药物主要应考虑用于急性激越患者的短期镇静,但不应用于精神分裂症和相关障碍的中、长期药物治疗中的抗精神病药物增强。