The long-term efficacy and tolerability of donepezil in patients with vascular dementia
Autor: | Karyn Boundy, David Wilkinson, Holly Posner, Dinesh Kumar, Rachel Schindler, Gustavo C. Roman, Stephen Salloway, Jane Hecker |
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Rok vydání: | 2010 |
Předmět: |
Male
medicine.medical_specialty Nausea Neuropsychological Tests Central nervous system disease Cognition Pharmacotherapy Double-Blind Method Piperidines Alzheimer Disease Internal medicine mental disorders medicine Humans Donepezil Adverse effect Vascular dementia Aged Psychiatric Status Rating Scales business.industry Dementia Vascular medicine.disease Surgery Psychiatry and Mental health Tolerability Indans Ambulatory Female Cholinesterase Inhibitors Geriatrics and Gerontology medicine.symptom business medicine.drug |
Zdroj: | International Journal of Geriatric Psychiatry. 25:305-313 |
ISSN: | 1099-1166 0885-6230 |
DOI: | 10.1002/gps.2340 |
Popis: | Objective To determine the long-term tolerability and efficacy of donepezil in patients with vascular dementia (VaD). Methods International, multicentre, open-label, 30-week extension study of two 24-week, randomised, double-blind, placebo-controlled studies. Participants were ambulatory adults (59% female; mean age, 74.7 ± 0.3) with a diagnosis of possible or probable VaD and without a diagnosis of Alzheimer's disease, who were medically stable and had completed one of two double-blind studies. All patients received donepezil 5 mg/day for the first 6 weeks, then 10 mg/day (clinician approval required). Assessments were performed at week 6 and every 12 weeks thereafter. The main outcome measure was the Alzheimer's disease Assessment Scale-cognitive subscale (ADAS-cog). Safety/tolerability measures included adverse events (AEs) and physical and laboratory evaluations. Results Of 1219 eligible patients, 885 (72.6%) were enrolled, of which 707 (79.9%) completed the study; 127 (14.4%) patients discontinued due to AEs. A mean reduction (0.6–1.15 points) from double-blind study baseline score to week 54 (end of open-label study) on the ADAS-cog was observed for patients who received donepezil continuously for 54 weeks. ADAS-cog scores remained stable in the group that initiated donepezil treatment during the extension study. Most common donepezil-related AEs were nausea (occurring in 5.3%) and diarrhoea (8.8%); no unexpected AEs attributable to donepezil occurred. Conclusion These data suggest that donepezil improves cognition for up to 54 weeks in patients with VaD. Patients initiating donepezil in this extension study did not perform as well on the primary outcome measure as those initiating donepezil in the double-blind study. Copyright © 2009 John Wiley & Sons, Ltd. |
Databáze: | OpenAIRE |
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