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Efficacy and safety of aripiprazole augmentation of clozapine in schizophrenia: A systematic review and meta-analysis of randomized-controlled trials

机译:阿立哌唑增强氯氮平在精神分裂症中的疗效和安全性:随机对照试验的系统评价和荟萃分析

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Limited options are available for clozapine-resistant schizophrenia and intolerable side effects of clozapine. We conducted a systematic review of randomized-controlled trials (RU's) to determine the efficacy and safety of aripiprazole augmentation of clozapine for schizophrenia. Electronic databases searched included PubMed, Scopus, Cochrane Central Register of Controlled Trials, Cumulative Index to Nursing and Allied Health Literature (CINAHL), and Web of Science. This review synthesized the data of four short-term (8-24 weeks), placebo-controlled trials (N = 347). The overall relative risk (RR, 95% confidence interval) of discontinuation rates was not significantly different between groups (RR = 1.41, 95% CI = 0.78 to 2.56). The pooled standardized mean differences (SMDs, 95% CIs) (Z-test; number of study; I-2-index) suggested trends of aripiprazole augmentation benefits on overall psychotic [-0.40 (-0.87 to 0.07) (n = 3; Z = 1.68, p = 0.09; I-2 = 68%)], positive [-1.05 (-2.39 to 029) (n = 3; Z = 1.54, p = 0.12; I-2 = 94%)], and negative [-0.36 (-0.77 to 0.05) (n = 3; Z = 1.74, p = 0.08; I-2 = 54%)] symptoms. Despite of no benefit on three cardiometabolic indices (i.e., fasting plasma glucose, triglyceride, and high-density lipoprotein), aripiprazole augmentation was superior for weight change with a mean difference (95% CI) of -1.36 kg (-2.35 to -0.36) (n = 3; Z = 2.67, p = 0.008; I-2 = 39%) and LDL-cholesterol with a mean difference of -11.06 mg/dL (-18.25 to -3.87) (n = 3; Z = 3.02, p = 0.003; I-2 = 31%). Aripiprazole augmentation was not correlated with headache and insomnia but significantly associated with agitation/akathesia (RR = 7.59, 95% CI = 1.43 to 40.18) (n = 3; Z = 238, p = 0.02; I-2 = 0%) and anxiety (RR = 2.70, 95% CI = 1.02 to 7.15) (n = 1; Z = 2.00, p = 0.05). The limited short-term data suggested that aripiprazole augmentation of clozapine can minimize the cardiometabolic risk, causes agitation/akathesia, and may be effective in attenuating psychotic symptoms. (C) 2015 Elsevier Ltd. All rights reserved.
机译:对于氯氮平耐药的精神分裂症和氯氮平无法耐受的副作用,提供的选择有限。我们对随机对照试验(RU's)进行了系统评价,以确定阿立哌唑增强氯氮平治疗精神分裂症的疗效和安全性。搜索的电子数据库包括PubMed,Scopus,Cochrane对照试验中央注册系统,护理和相关健康文献累积索引(CINAHL)和Web of Science。该评价综合了四个短期(8-24周)安慰剂对照试验(N = 347)的数据。各组间断率的总体相对风险(RR,95%置信区间)无显着差异(RR = 1.41,95%CI = 0.78至2.56)。汇总的标准化平均差异(SMD,95%CI)(Z检验;研究数量; I-2-指数)表明,阿立哌唑增加获益对整体精神病患者的趋势[-0.40(-0.87至0.07)(n = 3; n = 3; n = 3。 Z = 1.68,p = 0.09; I-2 = 68%)],正[-1.05(-2.39至029)(n = 3; Z = 1.54,p = 0.12; I-2 = 94%)],和阴性[-0.36(-0.77至0.05)(n = 3; Z = 1.74,p = 0.08; I-2 = 54%)]症状。尽管对三种心脏代谢指数(即空腹血糖,甘油三酸酯和高密度脂蛋白)无益处,但阿立哌唑增加的体重改变效果更好,平均差异(95%CI)为-1.36 kg(-2.35至-0.36 )(n = 3; Z = 2.67,p = 0.008; I-2 = 39%)和LDL-胆固醇的平均差为-11.06 mg / dL(-18.25至-3.87)(n = 3; Z = 3.02 ,p = 0.003; I-2 = 31%。阿立哌唑的增加与头痛和失眠无关,但与躁动/感觉异常显着相关(RR = 7.59,95%CI = 1.43至40.18)(n = 3; Z = 238,p = 0.02; I-2 = 0%)和焦虑(RR = 2.70,95%CI = 1.02至7.15)(n = 1; Z = 2.00,p = 0.05)。有限的短期数据表明,阿立哌唑增加氯氮平可以最大程度地降低心脏代谢风险,引起躁动/麻醉,并可能有效减轻精神病症状。 (C)2015 Elsevier Ltd.保留所有权利。

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