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首页> 外文期刊>Neuropsychiatric Disease and Treatment >Effectiveness and tolerability of transdermal rivastigmine in the treatment of Alzheimer’s disease in daily practice
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Effectiveness and tolerability of transdermal rivastigmine in the treatment of Alzheimer’s disease in daily practice

机译:日常实践中,经皮卡巴拉汀治疗阿兹海默氏病的有效性和耐受性

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Background: Oral cholinesterase inhibitors at doses efficacious for the treatment of Alzheimer’s disease (AD) are often prematurely discontinued due to gastrointestinal side effects. In controlled clinical trials, transdermal rivastigmine demonstrated less such effects at similar efficacy. The current study aimed to verify the validity of this data in daily practice.Methods: This was a prospective, multicenter, observational study on transdermal rivastigmine in Germany. Eligible patients were those with AD who had not yet been treated with rivastigmine. Outcome measures were changes in clock-drawing test, Mini-Mental State Examination (MMSE), Caregiver Burden Scale, Clinical Global Impression (CGI), physicians’ assessments of tolerability, and the incidence of adverse events (AEs) over 4 months of treatment.Results: In 257 centers 1113 patients were enrolled; 614 women and 499 men, mean age 76.5 years. In 58% of patients AD was treated for the first time and in 42% therapy was switched to transdermal rivastigmine, mostly due to lack of tolerability (13.6%) or effectiveness (26.9%). After 4 months, 67.4% of patients were on the target dose of 9.5 mg/day and 21.8% were still on 4.6 mg/day. MMSE significantly improved in patients with and without pretreatment (ΔMMSE, 0.9 ± 3.4 and 0.8 ± 3.4, respectively, both P < 0.001); the CGI score improved in 60.9% and 61.3% of patients, respectively. Overall 11.7% of patients had AEs, mainly affecting the skin or the gastrointestinal tract; in 1.1% of cases AEs were serious; 14.7% of patients discontinued therapy, 6.0% due to AEs. With rivastigmine treatment the percentage of patients taking psychotropic comedication decreased, particularly in first-time treated rivastigmine patients (from 27.1% to 22.6%; P < 0.001).Conclusion: Results were in line with data from controlled clinical trials. Switching from any other oral acetylcholinesterase inhibitor to transdermal rivastigmine may improve cognition.
机译:背景:由于胃肠道副作用,通常会过早停用口服胆碱酯酶抑制剂,以有效治疗阿尔茨海默氏病(AD)。在对照的临床试验中,经皮卡巴拉汀证明具有相似疗效的这种作用较少。目前的研究旨在验证该数据在日常实践中的有效性。方法:这是德国对透皮卡巴拉汀的一项前瞻性,多中心,观察性研究。合格的患者是尚未接受卡巴拉汀治疗的AD患者。结果指标包括抽签测试,小精神状态检查(MMSE),照顾者负担量表,临床总体印象(CGI),医生对耐受性的评估以及治疗4个月内不良事件(AEs)的发生率的变化结果:在257个中心中,有1113例患者入选;女性614位,男性499位,平均年龄76.5岁。在58%的患者中,AD是首次接受治疗,在42%的患者中,治疗方法转为使用卡巴拉汀经皮,主要是由于缺乏耐受性(13.6%)或有效性(26.9%)。 4个月后,有67.4%的患者使用9.5 mg /天的目标剂量,而21.8%的患者仍在4.6 mg /天的目标剂量下。接受和不接受预处理的患者的MMSE均显着改善(ΔMMSE分别为0.9±3.4和0.8±3.4,均P <0.001); CGI评分分别提高了60.9%和61.3%的患者。总体上,有11.7%的患者患有AE,主要影响皮肤或胃肠道。在1.1%的案例中,不良事件是严重的; 14.7%的患者中止治疗,其中6.0%由于AEs。使用rivastigmine治疗后,服用精神药物的患者比例有所下降,特别是在首次接受治疗的rivastigmine患者中(从27.1%降至22.6%; P <0.001)。结论:结果与对照临床试验的数据一致。从任何其他口服乙酰胆碱酯酶抑制剂换成透皮利凡斯的明可改善认知。

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