TY - JOUR
T1 - Quetiapine treatmdnt for behavioural and psychological symptoms of dementia in alzheimer's disease patients
T2 - A 6-week, double-blind, placebo-controlled study
AU - Paleacu, D.
AU - Barak, Y.
AU - Mirecky, I.
AU - Mazeh, D.
PY - 2008/4
Y1 - 2008/4
N2 - Setting: Treating elderly patients with Alzheimer's disease (AD) and behavioral and psychological symptoms of dementia (BPSD) is challenging due to the increased risk of iatrogenic movement disorders with old neuroleptics and the seemingly increasing risk of cardiovascular events with newer atypical agents. Quetiapine is an atypical antipsychotic agent that warrants further investigation. Objectives: To assess tolerability, safety, and clinical benefit of quetiapine in AD patients with BPSD. Participants and design: AD patients with BPSD participated in a 6-week randomized, double-blind, placebo-controlled trial. Quetiapine was increased on the basis of clinical response and tolerability. Primary efficacy assessments included the Neuropsychiatric Inventory (NPI) and Clinical Global Impression of Change (CGI-C). Secondary efficacy measures included the Mini-Mental State Examination (MMSE), the Simpson-Angus Scale (SAS) and the Abnormal Involuntary Movement Scale (AIMS). Results: Forty patients (26 women), mean age 82.2 (SD 6.4) years were enrolled, 27 completed treatment. Median dose of quetiapine was 200mg/ day. Significant NPI total scores reductions (79% for placebo and 68.5% for quetiapine) were observed. The CGI-C score decreased significantly in the quetiapine group (p = 0.009 at 6 weeks) and did not change significantly in the placebo group (p = 0.48). The MMSE, AIMS, SAS scores and adverse events did not differ significantly between the two arms. Conclusions: Quetiapine did not significantly improve Us psychosis scores. It did not cause cognitive and motor deterioration. These results might possibly be due to small sample size.
AB - Setting: Treating elderly patients with Alzheimer's disease (AD) and behavioral and psychological symptoms of dementia (BPSD) is challenging due to the increased risk of iatrogenic movement disorders with old neuroleptics and the seemingly increasing risk of cardiovascular events with newer atypical agents. Quetiapine is an atypical antipsychotic agent that warrants further investigation. Objectives: To assess tolerability, safety, and clinical benefit of quetiapine in AD patients with BPSD. Participants and design: AD patients with BPSD participated in a 6-week randomized, double-blind, placebo-controlled trial. Quetiapine was increased on the basis of clinical response and tolerability. Primary efficacy assessments included the Neuropsychiatric Inventory (NPI) and Clinical Global Impression of Change (CGI-C). Secondary efficacy measures included the Mini-Mental State Examination (MMSE), the Simpson-Angus Scale (SAS) and the Abnormal Involuntary Movement Scale (AIMS). Results: Forty patients (26 women), mean age 82.2 (SD 6.4) years were enrolled, 27 completed treatment. Median dose of quetiapine was 200mg/ day. Significant NPI total scores reductions (79% for placebo and 68.5% for quetiapine) were observed. The CGI-C score decreased significantly in the quetiapine group (p = 0.009 at 6 weeks) and did not change significantly in the placebo group (p = 0.48). The MMSE, AIMS, SAS scores and adverse events did not differ significantly between the two arms. Conclusions: Quetiapine did not significantly improve Us psychosis scores. It did not cause cognitive and motor deterioration. These results might possibly be due to small sample size.
KW - Alzheimer disease
KW - Psychosis
KW - Quetiapine
UR - http://www.scopus.com/inward/record.url?scp=42449163912&partnerID=8YFLogxK
U2 - 10.1002/gps.1892
DO - 10.1002/gps.1892
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C2 - 17879256
AN - SCOPUS:42449163912
SN - 0885-6230
VL - 23
SP - 393
EP - 400
JO - International Journal of Geriatric Psychiatry
JF - International Journal of Geriatric Psychiatry
IS - 4
ER -