...
首页> 外文期刊>The Lancet >Donepezil in patients with severe Alzheimer's disease: double-blind, parallel-group, placebo-controlled study.
【24h】

Donepezil in patients with severe Alzheimer's disease: double-blind, parallel-group, placebo-controlled study.

机译:多奈哌齐用于重度阿尔茨海默氏病患者:双盲,平行组,安慰剂对照研究。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: The cholinesterase inhibitor donepezil is used to treat mild-to-moderate Alzheimer's disease. Its efficacy in severe dementia has not been assessed and is controversial. Our aim was to ascertain the effectiveness of donepezil in patients with severe Alzheimer's disease, by focusing primarily on cognition and activities of daily living. METHODS: We did a 6-month, double-blind, parallel-group, placebo-controlled study in 248 patients with severe Alzheimer's disease (mini mental state examination score 1-10) who were living in assisted care nursing homes ran by trained staff in Sweden. We assigned patients oral donepezil (5 mg per day for 30 days then up to 10 mg per day thereafter, n=128) or matched placebo (n=120). Our primary endpoints were change from baseline to month 6 in the severe impairment battery (SIB) and modified Alzheimer's Disease Cooperative Study activities of daily living inventory for severe Alzheimer's disease (ADCS-ADL-severe). We analysed outcomes for patients with data at baseline and at one or more other timepoints (modified intent-to-treat population) with last observation carried forward used to replace missing data. FINDINGS: 95 patients assigned donepezil and 99 patients assigned placebo completed the study. Patients treated with donepezil improved more in SIB scores and declined less in ADCS-ADL-severe scores at 6 months after initiation of treatment compared with baseline than did controls (least squares [LS] mean difference, 5.7, 95% CI 1.5-9.8; p=0.008, and 1.7, 0.2-3.2; p=0.03, respectively). The incidence of adverse events was comparable between groups (donepezil 82% [n=105] vs placebo 76% [n=91]), with most being transient and mild or moderate in severity. More patients discontinued treatment because of adverse events in the donepezil group (n=20) than in the placebo group (n=8). INTERPRETATION: Donepezil improves cognition and preserves function in individuals with severe Alzheimer's disease who live in nursing homes.
机译:背景:胆碱酯酶抑制剂多奈哌齐用于治疗轻度至中度的阿尔茨海默氏病。其在重度痴呆症中的疗效尚未评估,尚有争议。我们的目标是通过主要关注认知和日常生活活动来确定多奈哌齐在重度阿尔茨海默氏病患者中的有效性。方法:我们对248名重度阿尔茨海默氏病(心理状态评分为1-10)的重度阿尔茨海默氏病患者进行了为期6个月的双盲,平行组,安慰剂对照研究,这些患者生活在训练有素的工作人员经营的辅助护理院在瑞典。我们为患者分配口服多奈哌齐(每天5 mg,共30天,之后每天最多10 mg,n = 128)或匹配的安慰剂(n = 120)。我们的主要终点指标是从严重损伤电池(SIB)的基线到第6个月的变化,以及针对重度阿尔茨海默氏病(ADCS-ADL-severe)的日常生活清单改良的阿尔茨海默氏病合作研究活动。我们分析了在基线和一个或多个其他时间点(经修改的意向性治疗人群)的数据患者的结局,并进行了最后一次观察以替代丢失的数据。结果:95名患者分配了多奈哌齐,99名患者分配了安慰剂,完成了研究。与基线相比,接受多奈哌齐治疗的患者在开始治疗后6个月时的SIB得分提高了更多,而ADCS-ADL-严重得分的下降却比对照组要少(最小二乘法[LS]平均差异5.7,95%CI 1.5-9.8; p = 0.008,以及1.7、0.2-3.2; p = 0.03)。各组之间不良事件的发生率相当(多奈哌齐82%[n = 105]与安慰剂76%[n = 91]),大多数为暂时性,轻度或中度。多奈哌齐组(n = 20)因不良事件而终止治疗的患者比安慰剂组(n = 8)更多。解释:多奈哌齐可改善居住在疗养院中的重度阿尔茨海默氏病患者的认知并保持其功能。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号