Memantine effects on behaviour in moderately severe to severe Alzheimer’s disease: a post-marketing surveillance study
- نوع فایل : کتاب
- زبان : انگلیسی
- مؤلف : Francesca Clerici • Nicola Vanacore • Antonietta Elia • Stefania Spila-Alegiani • Simone Pomati • Roberto Da Cas • Roberto Raschetti • Claudio Marian
- چاپ و سال / کشور: 2011
Description
The aim of this study is to evaluate memantine effectiveness on behavioural and psychological symptoms of dementia (BPSD) in clinical practice and to identify variables that may predict the therapy effects. The effects of memantine on behaviour were analysed in the database of a post-marketing surveillance study promoted by the Lombardy Region Health Office and involving 43 Alzheimer’s disease (AD) Units. From July to December 2005, 399 moderately severe-to-severe AD patients free of cholinergic medications were enrolled, treated with memantine and followed-up for 6 months. BPSD were assessed in a subgroup of 297 patients [mean age 77 ± 8 years; 73% females; mean neuropsychiatric inventory (NPI) score 28 ± 24] for whom the 12-item NPI subscores at baseline, and at 3 and 6 months were available. The 12 BPSD were clustered as follows: affect, physical behaviour, psychosis and hypomania. The main outcome measure was the proportion of individual cluster responders at 6 months of therapy. The proportion of individual cluster responders was 30% affect, 24% physical behaviour, 29% psychosis, 27% hypomania. Patients taking 20 mg memantine daily during the study period had a statistically significant higher probability to experience behavioural improvement than those who discontinued treatment or did not complete memantine titration (affect OR 9.0; 95% CI 3.8–21.6; physical behaviour OR 17.8; 95% CI 5.9–53.6; psychosis OR 23.6; 95% CI 5.1–110.8). The logistic regression analysis was not applicable to the hypomania subsyndrome because of the low cluster prevalence. The standard 20 mg daily memantine treatment regimen was found to be associated with a modest 6-month behavioural improvement in the affect, physical behaviour and psychosis domains in 24–30% of patients.
Neurol Sci DOI 10.1007/s10072-011-0618-0 Received: 19 February 2011 / Accepted: 28 April 2011
