Efficacy and safety of atypical antipsychotic drug treatment for dementia: a systematic review and meta-analysis.

IF 7.6 1区 医学 Q1 CLINICAL NEUROLOGY Alzheimer's Research & Therapy Pub Date : 2015-04-20 eCollection Date: 2015-01-01 DOI:10.1186/s13195-015-0102-9
Lin Tan, Lan Tan, Hui-Fu Wang, Jun Wang, Chen-Chen Tan, Meng-Shan Tan, Xiang-Fei Meng, Chong Wang, Jin-Tai Yu
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引用次数: 39

Abstract

Introduction: A wide variety of atypical antipsychotic drugs (risperidone, olanzapine, quetiapine, aripiprazole, ziprasidone and clozapine) are widely used in the management of neuropsychiatric symptoms, which are commonly seen in dementia, but results from randomised controlled trials (RCTs) on the efficacy and safety of these agents are conflicting. We aimed to quantify the efficacy and safety of atypical antipsychotic drugs on neuropsychiatric symptoms in dementia patients.

Methods: PubMed, EMBASE, the Cochrane Controlled Trials Register and the Cochrane Database of Systematic Reviews for reports published before August 2014 were searched for eligible randomized controlled trials of atypical antipsychotic drugs therapy in patients with psychotic symptoms of dementia. Two reviewers independently assessed the quality of the trials and extracted information.

Results: Overall, 23 relevant RCTs with 5,819 participants were identified. This meta-analysis demonstrated a significant efficacy of atypical antipsychotics on psychiatric symptoms and cognitive functions compared to placebo. In the meta-analysis, the weighted mean differences (WMDs) in change scores for psychiatric symptoms were in favor of aripiprazole (-4.4, 95% confidence interval (CI) - 7.04 to -1.77) and risperidone (-1.48, 95% CI -2.35 to -0.61) compared to placebo. In cognitive effects, WMDs in change scores for the Clinical Global Impression-Change (CGI-C) were in favor of aripiprazole, risperidone, olanzapine and quetiapine which ranged from a -0.30 points mean difference (95% CI:-0.59 to -0.01) in the aripiprazole trials to -0.43 (95% CI:-0.62 to -0.25) in the risperidone group. Patients receiving atypical antipsychotics showed no difference in risk for injuries or falls (P > 0.05), significantly higher risks (P < 0.05) for somnolence, urinary tract infection, edema and abnormal gait. However, there was no significant evidence for death reported.

Conclusion: Aripiprazole and risperidone are able to improve psychiatric symptoms and slow decline in cognition function at average 12 weeks in patients with neuropsychiatric symptoms of dementia. However, high adverse events may offset the efficacy of atypical antipsychotics in dementia.

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非典型抗精神病药物治疗痴呆的疗效和安全性:一项系统回顾和荟萃分析。
各种非典型抗精神病药物(利培酮、奥氮平、喹硫平、阿立哌唑、齐拉西酮和氯氮平)被广泛用于治疗神经精神症状,这些症状常见于痴呆,但随机对照试验(RCTs)关于这些药物的疗效和安全性的结果是相互矛盾的。我们旨在量化非典型抗精神病药物对痴呆患者神经精神症状的疗效和安全性。方法:检索PubMed、EMBASE、Cochrane对照试验注册库(Cochrane Controlled Trials Register)和Cochrane系统评价数据库(Cochrane Database of Systematic Reviews)中2014年8月前发表的报告,寻找符合条件的非典型抗精神病药物治疗精神病性痴呆症状患者的随机对照试验。两名审稿人独立评估试验的质量并提取信息。结果:共纳入23项相关随机对照试验,共纳入5819名受试者。这项荟萃分析表明,与安慰剂相比,非典型抗精神病药物对精神症状和认知功能有显著的疗效。在荟萃分析中,与安慰剂相比,精神症状变化评分的加权平均差异(wmd)有利于阿立哌唑(-4.4,95%可信区间(CI) - 7.04至-1.77)和利培酮(-1.48,95% CI -2.35至-0.61)。在认知效果方面,临床总体印象变化(CGI-C)评分的WMDs有利于阿立哌唑、利培酮、奥氮平和喹硫平,阿立哌唑组的平均差异为-0.30分(95% CI:-0.59至-0.01),而利培酮组的平均差异为-0.43分(95% CI:-0.62至-0.25)。结论:阿立哌唑和利培酮可改善痴呆神经精神症状患者平均12周的精神症状,减缓认知功能下降。然而,高不良事件可能抵消非典型抗精神病药物对痴呆的疗效。
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来源期刊
Alzheimer's Research & Therapy
Alzheimer's Research & Therapy 医学-神经病学
CiteScore
13.10
自引率
3.30%
发文量
172
审稿时长
>12 weeks
期刊介绍: Alzheimer's Research & Therapy is an international peer-reviewed journal that focuses on translational research into Alzheimer's disease and other neurodegenerative diseases. It publishes open-access basic research, clinical trials, drug discovery and development studies, and epidemiologic studies. The journal also includes reviews, viewpoints, commentaries, debates, and reports. All articles published in Alzheimer's Research & Therapy are included in several reputable databases such as CAS, Current contents, DOAJ, Embase, Journal Citation Reports/Science Edition, MEDLINE, PubMed, PubMed Central, Science Citation Index Expanded (Web of Science) and Scopus.
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