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认知增强剂治疗阿尔茨海默病的疗效:系统评价和网络荟萃分析方案。

Efficacy of cognitive enhancers for Alzheimer's disease: protocol for a systematic review and network meta-analysis.

机构信息

Li Ka Shing Knowledge Institute, St, Michael's Hospital, 209 Victoria Street, East Building, Toronto, ON, M5B 1T8, Canada.

出版信息

Syst Rev. 2012 Jun 28;1:31. doi: 10.1186/2046-4053-1-31.

Abstract

BACKGROUND

Approximately 35 million people world-wide have Alzheimer's disease and this is projected to nearly double by 2030. Cognitive enhancers, including cholinesterase inhibitors (for example, donepezil, galantamine and rivastigmine) and memantine (N-methyl-D-aspartic acid (NMDA) receptor antagonist) have been approved for the treatment of Alzheimer's disease in many countries. Our objective is to evaluate the comparative effectiveness, safety, and cost of cognitive enhancers for Alzheimer's disease through a systematic review.

METHODS/DESIGN: Studies examining the efficacy, safety, and cost of cognitive enhancers compared to placebo, supportive care, and other cognitive enhancers for Alzheimer's patients will be included. The primary outcome is cognition and secondary outcomes include function, behavior, quality of life, safety, and cost. Experimental studies (randomized controlled trials, quasi-randomized controlled trials, controlled clinical trials), quasi-experimental studies (controlled before-after, interrupted time series), and observational studies (cohort, case-control studies) will be eligible for inclusion. Inclusion will not be limited by publication status, time period or language of dissemination.We will search electronic databases (for example, MEDLINE, Cochrane Central Register of Controlled Trials, EMBASE, CINAHL, Ageline) from inception onwards. The electronic database search will be supplemented by searching for grey literature (for example, conference proceedings, searches in Google and relevant organization websites). Two reviewers will independently screen the studies for inclusion using the eligibility criteria established a priori and independently extract data. Risk of bias will be assessed using the Cochrane Risk of Bias tool for experimental and quasi-experimental studies and the Newcastle Ottawa Scale for observational studies. If deemed appropriate, meta-analysis and network (that is, indirect comparisons) meta-analysis will be conducted.

DISCUSSION

Our systematic review will inform the decision of healthcare providers, policy-makers, Alzheimer's patients and family members about the use of cognitive enhancers, by improving their understanding of the costs, benefits and harms that are associated with these agents. PROSPERO REGISTRY NUMBER: CRD42012001948.

摘要

背景

全球约有 3500 万人患有阿尔茨海默病,预计到 2030 年这一数字将翻一番。在许多国家,认知增强剂,包括胆碱酯酶抑制剂(例如多奈哌齐、加兰他敏和利伐斯的明)和盐酸美金刚(N-甲基-D-天冬氨酸(NMDA)受体拮抗剂)已被批准用于治疗阿尔茨海默病。我们的目标是通过系统评价评估认知增强剂治疗阿尔茨海默病的有效性、安全性和成本。

方法/设计:将纳入研究比较了认知增强剂与安慰剂、支持性护理和其他用于治疗阿尔茨海默病患者的认知增强剂的疗效、安全性和成本。主要结局是认知,次要结局包括功能、行为、生活质量、安全性和成本。实验研究(随机对照试验、准随机对照试验、对照临床试验)、准实验研究(对照前后、间断时间序列)和观察性研究(队列、病例对照研究)将有资格纳入。纳入将不受出版状态、时间段或传播语言的限制。我们将从成立之初开始搜索电子数据库(例如,MEDLINE、Cochrane 对照试验中心注册库、EMBASE、CINAHL、Ageline)。电子数据库搜索将通过搜索灰色文献(例如会议记录、在 Google 中的搜索和相关组织网站)进行补充。两名审查员将使用事先确定的纳入标准独立筛选研究,并独立提取数据。将使用 Cochrane 实验和准实验研究偏倚风险工具以及 Newcastle-Ottawa 量表对观察性研究进行偏倚风险评估。如果认为合适,将进行荟萃分析和网络(即间接比较)荟萃分析。

讨论

我们的系统评价将通过提高医疗保健提供者、政策制定者、阿尔茨海默病患者及其家属对这些药物的成本、益处和危害的理解,为他们使用认知增强剂提供信息。PROSPERO 注册号:CRD42012001948。

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