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评估高剂量13.3毫克/24小时卡巴拉汀透皮贴剂对重度阿尔茨海默病患者的疗效。

Evaluating Response to High-Dose 13.3 mg/24 h Rivastigmine Patch in Patients with Severe Alzheimer's Disease.

作者信息

Farlow Martin R, Sadowsky Carl H, Velting Drew M, Meng Xiangyi, Islam M Zahur

机构信息

Department of Neurology, Indiana University School of Medicine, Indianapolis, IN, USA.

Division of Neurology, Nova Southeastern University, Fort Lauderdale, FL, USA.

出版信息

CNS Neurosci Ther. 2015 Jun;21(6):513-9. doi: 10.1111/cns.12385. Epub 2015 Feb 10.

Abstract

AIMS

To identify factors predicting improvement/stabilization on the Alzheimer's Disease Cooperative Study-Clinical Global Impression of Change (ADCS-CGIC) and investigate whether early treatment responses can predict long-term outcomes, during a trial of 13.3 mg/24 h versus 4.6 mg/24 h rivastigmine patch in patients with severe Alzheimer's disease (AD).

METHODS

Logistic regression was used to relate Week 24 ADCS-CGIC score to potential baseline predictors. Additional analyses based on receiver-operating characteristic curves were performed using Week 8/16 ADCS-CGIC scores to predict response (13.3 mg/24 h patch) at Week 24. ADCS-CGIC score of (1) 1-3 = "improvement," (2) 1-4 = "improvement or no change".

RESULTS

"Treatment" (13.3 mg/24 h patch) and increased age were significant predictors of "improvement" (P = 0.01 and P = 0.003, respectively), and "treatment" (P = 0.001), increased age (P = 0.002), and prior AD treatment (P = 0.03) for "improvement or no change". At Week 8 and 16, ADCS-CGIC scores of 4 and 5 were optimal thresholds in predicting "improvement," and "improvement or no change," respectively, at Week 24.

CONCLUSIONS

A significant therapeutic effect of high-dose rivastigmine patch on ADCS-CGIC response was observed. The 13.3 mg/24 h patch was identified as a predictor of "improvement" or "improvement or no change". Patients with minimal worsening/improvement/no change after treatment initiation may be more likely to respond following long-term therapy.

摘要

目的

在一项针对重度阿尔茨海默病(AD)患者的试验中,比较13.3毫克/24小时与4.6毫克/24小时的卡巴拉汀贴片,确定预测阿尔茨海默病协作研究 - 临床总体印象变化量表(ADCS - CGIC)改善/稳定的因素,并研究早期治疗反应是否能预测长期结果。

方法

采用逻辑回归分析将第24周的ADCS - CGIC评分与潜在的基线预测因素相关联。使用第8/16周的ADCS - CGIC评分进行基于受试者工作特征曲线的额外分析,以预测第24周的反应(13.3毫克/24小时贴片)。ADCS - CGIC评分:(1)1 - 3 =“改善”,(2)1 - 4 =“改善或无变化”。

结果

“治疗”(13.3毫克/24小时贴片)和年龄增加是“改善”的显著预测因素(分别为P = 0.01和P = 0.003),以及“治疗”(P = 0.001)、年龄增加(P = 0.002)和既往AD治疗(P = 0.03)是“改善或无变化”的预测因素。在第8周和第16周,ADCS - CGIC评分为4和5分别是预测第24周“改善”和“改善或无变化”的最佳阈值。

结论

观察到高剂量卡巴拉汀贴片对ADCS - CGIC反应有显著治疗效果。13.3毫克/24小时贴片被确定为“改善”或“改善或无变化”的预测因素。治疗开始后病情恶化最小/改善/无变化的患者可能更有可能在长期治疗后产生反应。

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