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阿尔茨海默病激越随机临床试验中使用的方法学文献综述。

A Literature Review of Methodologies Used in Randomized Clinical Trials of Agitation in Alzheimer's Disease.

机构信息

Sanjay Dubé, Avanir Pharmaceuticals, Inc., 30 Enterprise, Aliso Viejo, CA 92656, Tel: 949-389-6700, Fax: 949-643-6800, Email:

出版信息

J Prev Alzheimers Dis. 2018;5(2):120-133. doi: 10.14283/jpad.2018.17.

Abstract

Agitation is a common and burdensome symptom associated with Alzheimer's disease (AD). This is a narrative literature review of the designs and methods used in randomized clinical trials of agitation in patients with AD; sources range from published, to completed but not published, to ongoing studies in the past 10 years. Selection for review included blinded, randomized trials conducted to assess the effect of a pharmacological intervention for which agitation in patients with AD was among the prespecified end points. Key criteria for exclusion included open-label studies, trials of dementia not specific to AD, or mixed populations of AD and unspecified dementia. A search of PubMed and clinicaltrials.gov databases identified 36 trials for which agitation was among the prespecified end points: 18 were published trials and 18 were completed but not published or ongoing. There was significant heterogeneity among AD studies in terms of diagnostic criteria, assessment of severity of disease and agitation, sample size and powering assumptions, treatment duration, patient age and cognitive status, and outcomes measurements. Few studies used a mitigation strategy for placebo response. Accumulating evidence suggests that it is important to consider the following in trial design: thresholds for baseline severity of agitation and AD; use of prespecified accepted criteria to define agitation; and use of standardized, validated tools to measure treatment effects during a trial. Adoption of these design strategies might help improve signal detection and bring us closer to identifying the most appropriate, effective, and safe treatments for agitation in patients with AD.

摘要

激越症是阿尔茨海默病(AD)患者常见且令人痛苦的症状。本文对 10 年来 AD 患者激越症随机临床试验的设计和方法进行了叙述性文献回顾;资料来源包括已发表的、已完成但未发表的和正在进行的研究。纳入综述的标准为:旨在评估药物干预效果的盲法随机试验,且激越症为预先设定的终点之一。排除标准包括开放性研究、非 AD 特异性痴呆试验或 AD 和未特指痴呆混合人群研究。对 PubMed 和 clinicaltrials.gov 数据库的检索共确定了 36 项激越症为预先设定终点的试验:其中 18 项为已发表的试验,18 项为已完成但未发表或正在进行的试验。在 AD 研究中,诊断标准、疾病严重程度和激越症评估、样本量和效能假设、治疗持续时间、患者年龄和认知状态以及结局测量等方面存在显著异质性。很少有研究采用安慰剂反应缓解策略。越来越多的证据表明,在试验设计中需要考虑以下几点:激越症和 AD 基线严重程度的阈值;使用预先规定的公认标准来定义激越症;以及在试验期间使用标准化、经过验证的工具来测量治疗效果。采用这些设计策略可能有助于提高信号检测能力,并使我们更接近确定 AD 患者激越症最合适、最有效和最安全的治疗方法。

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