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首页> 外文期刊>American journal of psychiatry >Atypical antipsychotic augmentation in major depressive disorder: a meta-analysis of placebo-controlled randomized trials.
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Atypical antipsychotic augmentation in major depressive disorder: a meta-analysis of placebo-controlled randomized trials.

机译:主要抑郁症患者的非典型抗精神病药物增加:安慰剂对照随机试验的荟萃分析。

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OBJECTIVE: The authors sought to determine by meta-analysis the efficacy and tolerability of adjunctive atypical antipsychotic agents in major depressive disorder. METHOD: Searches were conducted of MEDLINE/PubMed (1966 to January 2009), the Cochrane database, abstracts of major psychiatric meetings since 2000, and online trial registries. Manufacturers of atypical antipsychotic agents without online registries were contacted. Trials selected were acute-phase, parallel-group, double-blind controlled trials with random assignment to adjunctive atypical antipsychotic or placebo. Patients had nonpsychotic unipolar major depressive disorder that was resistant to prior antidepressant treatment. Response, remission, and discontinuation rates were either reported or obtained. Data were extracted by one author and checked by the second. Data included study design, number of patients, patient characteristics, methods of establishing treatment resistance, drug doses, duration of the adjunctive trial, depression scale used, response and remission rates, and discontinuation rates for any reason or for adverse events. RESULTS: Sixteen trials with 3,480 patients were pooled using a fixed-effects meta-analysis. Adjunctive atypical antipsychotics were significantly more effective than placebo (response: odds ratio=1.69, 95% CI=1.46-1.95, z=7.00, N=16, p<0.00001; remission: odds ratio=2.00, 95% CI=1.69-2.37, z=8.03, N=16, p<0.00001). Mean odds ratios did not differ among the atypical agents and were not affected by trial duration or method of establishing treatment resistance. Discontinuation rates for adverse events were higher for atypical agents than for placebo (odds ratio=3.91, 95% CI=2.68-5.72, z=7.05, N=15, p<0.00001). CONCLUSIONS: Atypical antipsychotics are effective augmentation agents in major depressive disorder but are associated with an increased risk of discontinuation due to adverse events.
机译:目的:作者试图通过荟萃分析确定辅助性非典型抗精神病药在重度抑郁症中的疗效和耐受性。方法:对MEDLINE / PubMed(1966年至2009年1月),Cochrane数据库,自2000年以来的主要精神病学会议摘要以及在线试验注册进行了搜索。与没有在线注册的非典型抗精神病药制造商联系。选择的试验为急性期,平行组,双盲对照试验,随机分配给辅助性非典型抗精神病药或安慰剂。患者患有非精神病性单相重度抑郁症,对先前的抗抑郁药治疗有抵抗力。报告或获得反应,缓解和停药率。数据由一位作者提取,然后由第二位作者检查。数据包括研究设计,患者人数,患者特征,建立治疗耐药性的方法,药物剂量,辅助试验的持续时间,所用的抑郁量表,反应和缓解率以及因任何原因或不良事件导致的停药率。结果:采用固定效应荟萃分析汇总了16项针对3480例患者的试验。辅助性非典型抗精神病药的疗效显着高于安慰剂(反应:优势比= 1.69,95%CI = 1.46-1.95,z = 7.00,N = 16,p <0.00001;缓解:优势比= 2.00,95%CI = 1.69- 2.37,z = 8.03,N = 16,p <0.00001)。非典型药物之间的平均优势比没有差异,并且不受试验持续时间或建立抗药性的方法的影响。非典型药物不良事件的中止率高于安慰剂(赔率= 3.91,95%CI = 2.68-5.72,z = 7.05,N = 15,p <0.00001)。结论:非典型抗精神病药是重度抑郁症的有效增强剂,但与不良事件引起的停药风险增加有关。

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