Efficacy of Ginkgo biloba extract EGb 761(®) in dementia with behavioural and psychological symptoms: A systematic review.
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State: Public
Version: author
State: Public
Version: author
Serval ID
serval:BIB_5C435DD0F611
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Efficacy of Ginkgo biloba extract EGb 761(®) in dementia with behavioural and psychological symptoms: A systematic review.
Journal
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry
ISSN
1814-1412 (Electronic)
ISSN-L
1562-2975
Publication state
Published
Issued date
12/2016
Peer-reviewed
Oui
Volume
17
Number
8
Pages
622-633
Language
english
Notes
Publication types: Journal Article
Publication Status: ppublish
Publication Status: ppublish
Abstract
To review current evidence of efficacy of Ginkgo biloba extract EGb 761(®) in dementia with behavioural and psychological symptoms (BPSD).
Randomized, placebo-controlled trials assessing the effects of EGb 761(®) in dementia patients with BPSD were included if the diagnosis was made in accordance with internationally accepted criteria, the treatment period was at least 22 weeks, outcome measures covered BPSD and at least two of the following domains of assessment, i.e. cognition, activities of daily living and clinical global assessment, and methodological quality was adequate. An analysis of covariance (ANCOVA) model was used to calculate the pooled effect estimates and to compare effects of EGb 761(®) and placebo; furthermore, combined risk differences of response rates were calculated.
Four published trials were identified, involving altogether 1,628 outpatients with mild to moderate dementia. Least-square mean differences for change from baseline in cognition, BPSD (including caregiver distress rating), activities of daily living, clinical global impression, and quality of life favoured EGb 761(®) (P < 0.001 for all comparisons).
The pooled analyses provide evidence of efficacy of EGb 761(®) at a daily dose of 240 mg in the treatment of out-patients suffering from Alzheimer's, vascular or mixed dementia with BPSD.
Randomized, placebo-controlled trials assessing the effects of EGb 761(®) in dementia patients with BPSD were included if the diagnosis was made in accordance with internationally accepted criteria, the treatment period was at least 22 weeks, outcome measures covered BPSD and at least two of the following domains of assessment, i.e. cognition, activities of daily living and clinical global assessment, and methodological quality was adequate. An analysis of covariance (ANCOVA) model was used to calculate the pooled effect estimates and to compare effects of EGb 761(®) and placebo; furthermore, combined risk differences of response rates were calculated.
Four published trials were identified, involving altogether 1,628 outpatients with mild to moderate dementia. Least-square mean differences for change from baseline in cognition, BPSD (including caregiver distress rating), activities of daily living, clinical global impression, and quality of life favoured EGb 761(®) (P < 0.001 for all comparisons).
The pooled analyses provide evidence of efficacy of EGb 761(®) at a daily dose of 240 mg in the treatment of out-patients suffering from Alzheimer's, vascular or mixed dementia with BPSD.
Pubmed
Create date
31/08/2015 13:36
Last modification date
20/08/2019 14:14