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BukuTreatment of dementia and mild cognitive impairment with or without cerebrovascular disease: Expert consensus on the use of Ginkgo biloba extract, EGb 761® (article of CNS Neuroscience and Therapeutics Vol25, Iss2 Feb 2019 P.288-298)
Bibliografi
Author: Kandiah, Nagaendran ; Ong, Paulus Anam ; Turana, Yuda ; Li-Ling Ng ; Mamun, Kaysar ; Merchant, Reshma Aziz ; Chen, Christopher ; Dominguez, Jacqueline ; Marasigan, Simeon ; Ampil, Encarnita ; Nguyen, Van Thong ; Yusoff, Suraya ; Yee Fai Chan ; Fee Mann Yong ; Krairit, Orapitchaya ; Suthisisang, Chuthamanee ; Senanarong, Vorapun ; Yong Ji ; Thukral, Ramesh ; Ihl, Ralf
Topik: Alzheimer disease; cerebrovascular disease; dementia; EGb 761®; Ginkgo biloba; JABFUNG-FKIK-YDT-2021-08
Bahasa: (EN )    
Penerbit: John Wiley & Sons Ltd     Tempat Terbit: England    Tahun Terbit: 2018    
Jenis: Article - diterbitkan di jurnal ilmiah internasional
Fulltext:
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Abstract
Background

The Ginkgo biloba special extract, EGb 761® has been widely used in the treatment of neuropsychiatric disorders, including Alzheimer’s disease (AD).

Methods

To guide clinical practice in the Asian region, the Asian Clinical Expert Group on Neurocognitive Disorders compiled evidence-based consensus recommendations regarding the use of EGb 761® in neurocognitive disorders with/without cerebrovascular disease.

Results

Key randomized trials and robust meta-analyses have demonstrated significant improvement in cognitive function, neuropsychiatric symptoms, activities of daily living (ADL) and quality of life with EGb 761®versus placebo in patients with mild-to-moderate dementia. In those with mild cognitive impairment (MCI), EGb 761® has also demonstrated significant symptomatic improvement versus placebo. World Federation of Societies of Biological Psychiatry guidelines list EGb 761® with the same strength of evidence as acetylcholinesterase inhibitors and N-methyl-D-aspartate (NMDA) antagonists e.g. memantine (Grade 3 recommendation; Level B evidence). Only EGb 761® had Level B evidence in improving cognition, behaviour, and ADL in both AD and vascular dementia patients. Safety analyses show EGb 761® to have a positive risk-benefit profile. While concerns have been raised regarding a possible increased bleeding risk, several randomized trials and two meta-analyses have not supported this association.

Conclusions

The Expert Group foresee an important role for EGb 761®, used alone or as an add-on therapy, in the treatment of MCI and dementias, particularly when patients do not derive benefit from acetylcholinesterase inhibitors or NMDA antagonists. EGb 761® should be used in alignment with local clinical practice guidelines.
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