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首页> 外文期刊>Dementia and Geriatric Cognitive Disorders Extra >A 24-Week, Randomized, Controlled Study to Evaluate the Tolerability, Safety and Efficacy of 2 Different Titration Schemes of the Rivastigmine Patch in Japanese Patients with Mild to Moderate Alzheimer's Disease
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A 24-Week, Randomized, Controlled Study to Evaluate the Tolerability, Safety and Efficacy of 2 Different Titration Schemes of the Rivastigmine Patch in Japanese Patients with Mild to Moderate Alzheimer's Disease

机译:为评估轻度至中度阿尔茨海默氏病日本患者2种不同滴定方案的Rivastigmine贴剂的耐受性,安全性和有效性,进行的24周随机对照研究

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Aim: To investigate whether 1-step titration of the rivastigmine patch (initiated at 5 cm2 and titrated to 10 cm2 after 4 weeks) is well tolerated in Japanese patients with Alzheimer's disease (AD) as compared to 3-step titration (initiated at 2.5 cm2 and titrated by 2.5 cm2 every 4 weeks to 10 cm2). Methods: A 24-week, multicenter, randomized, double-blind study was conducted in Japan between July 2012 and May 2014. Patients with mild to moderate AD aged 50-85 years were randomized 1:1 to 1-step or 3-step titration of the rivastigmine once-daily patch. The primary endpoint was the proportion of patients with adverse events leading to discontinuation. Results: Of 216 patients randomized, 215 (1-step, n = 107; 3-step, n = 108) were included in the safety analysis. The primary endpoint outcome was 15.0% in the 1-step group and 18.5% in the 3-step group. The observed treatment difference was ?3.6% (95% confidence interval: ?17.0, 9.6), falling within the prespecified acceptance range. Conclusion: The tolerability of two different titration schemes was similar in Japanese patients with AD.
机译:目的:研究在日本人群中,对rivastigmine贴剂的1步滴定(从5 cm 2 开始并在4周后滴定至10 cm 2 )是否耐受良好与3步滴定法相比(始于2.5 cm 2 ,每4周以2.5 cm 2 滴定至10 cm 2 ) sup>)。方法:2012年7月至2014年5月在日本进行了为期24周,多中心,随机,双盲的研究。年龄在50-85岁的轻度至中度AD患者被随机分为1:1至1步或3步每日一次贴剂卡巴拉汀的滴定。主要终点是发生不良事件导致停药的患者比例。结果:在随机分配的216例患者中,安全性分析包括215例(1步,n = 107; 3步,n = 108)。 1步组的主要终点结果为15.0%,3步组的主要终点结果为18.5%。观察到的治疗差异为3.6%(95%置信区间:17.0、9.6),处于预定的接受范围内。结论:两种不同的滴定方案对日本AD患者的耐受性相似。

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