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Efficacy and tolerability of topiramate-augmentation therapy for schizophrenia: a systematic review and meta-analysis of randomized controlled trials

机译:托吡酯增强疗法治疗精神分裂症的疗效和耐受性:随机对照试验的系统评价和荟萃分析

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摘要

This study aimed to perform a comprehensive meta-analysis of topiramate-augmentation therapy in patients with schizophrenia receiving antipsychotic agents. Data published up to June 20, 2016 were obtained from the PubMed, PsycINFO, and Cochrane Library databases. Twelve randomized controlled trials comparing topiramate to placebo or antipsychotic only were included (n=676 patients). The primary outcome was change in overall symptoms. Relative risk (RR) and standardized mean difference (SMD), along with 95% confidence intervals, were calculated using random effects model for each outcome. Topiramate-augmentation therapy was superior to the control for decreasing overall symptoms (SMD −0.55, 95% confidence interval −0.86 to −0.24; P=0.001; I2=55%, eight comparisons, n=380), positive symptoms (SMD −0.4), negative symptoms (SMD −0.47), and Positive and Negative Syndrome Scale general subscale scores (SMD −0.67). Furthermore, topiramate-augmentation therapy decreased weight (SMD −0.69) and body mass index (SMD −0.95) compared with the control. Topiramate was similar to the control with respect to discontinuation due to all causes (RR 1.19), inefficacy (RR 1.71), and adverse events (RR 1.09). Topiramate was associated with higher incidence of paresthesia (RR 2.67) and attention difficulty (RR 8.97) compared with the control. Our results seemed to suggest that topiramate-augmentation therapy improves the psychopathology of schizophrenia with good tolerability and has the additional advantage of weight maintenance. However, because there were some limitations (numbers of studies and patients included in the meta-analysis were small, some studies used completer analysis, Chinese studies were included in the meta-analysis, and studies that had a risk of bias were included in the meta-analysis) in this study, we cannot apply the results of this study in daily clinical practice.
机译:这项研究旨在对接受抗精神病药的精神分裂症患者进行托吡酯增强疗法进行全面的荟萃分析。截至2016年6月20日发布的数据来自PubMed,PsycINFO和Cochrane图书馆数据库。包括十二项随机对照试验,仅比较托吡酯与安慰剂或抗精神病药(n = 676例)。主要结果是总体症状的改变。使用随机效应模型针对每个结局计算相对风险(RR)和标准化平均差异(SMD),以及95%的置信区间。托吡酯增强疗法在减轻总体症状方面优于对照组(SMD -0.55,95%置信区间-0.86至-0.24; P = 0.001; I 2 = 55%,八次比较,n = 380),阳性症状(SMD -0.4),阴性症状(SMD -0.47)和阳性和阴性综合症量表的总体子量表得分(SMD -0.67)。此外,与对照组相比,托吡酯增强疗法可减轻体重(SMD -0.69)和体重指数(SMD -0.95)。由于所有原因(RR 1.19),无效(RR 1.71)和不良事件(RR 1.09)停药,托吡酯与对照组相似。与对照组相比,托吡酯与感觉异常的发生率高(RR 2.67)和注意困难(RR 8.97)相关。我们的结果似乎表明托吡酯增强疗法可改善精神分裂症的心理病理学,并具有良好的耐受性,并具有维持体重的其他优势。但是,由于存在一定的局限性(荟萃分析中的研究数量和患者人数很少,一些研究使用了更完整的分析,荟萃分析中包括了中文研究,而有偏倚风险的研究也包括在内。荟萃分析),我们不能将这项研究的结果应用于日常临床实践中。

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