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A Double-Blind, Placebo-Controlled Multicenter Study of Tacrine for Alzheimer's Dissease
NEJM 327:1253-1259, 13061992., Davis,K.L.,et al, 1992
See this aricle in Pubmed

Article Abstract
At the end of the six-week trial,the patients receiving tacrine had a mean adjusted cognitive-subscale score of 30.3(Alzheimer's Disease Assessment Scale)as compared with 32.7 in patients receiving placebo.This represents a smaller decline(by 2.4 points)in cognitive performance in the tacrine group(P<0.001).There were no differences between the groups in their global-rating scores.The tacrine group had a significantly smaller decline in the activities of daily living.The results of the Mini-Mental State Examination favored tacrine,but the differences were small and not statistically significant(a score of 16.0 with tacrine vs.15.3 with placebo;P=-.08).Gastrointestinal symptoms,elevation of aminotransferase levels,and headache were the most frequent side effects;all could be reversed by reducing the dose or discontinuing treatment.In this short- term study in patients with Alzheimer's disease who were selected for apparent responsiveness to tacrine,treatment with tacrine resulted in a statistically significant reduction in the decline of cognitive function, although this reduction was not large enough to be detected by the study physicians'global assessments of the patients.
 
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Alzheimer's disease
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dementia
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tetrahydroaminoacridine
treatment of neurologic disorder

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