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Real-World Use of Symptomatic Treatments in Early Alzheimer’s Disease

BACKGROUND: Alzheimer’s disease (AD) is the most common type of dementia, causing progressive decline of memory, thinking, and behavior, impairing daily functioning. Early AD (eAD) includes mild cognitive impairment (MCI) due to AD and mild AD dementia. OBJECTIVE: The aim of this study was to invest...

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Autores principales: Garcia, Maria João, Leadley, Regina, Lang, Shona, Ross, Janine, Vinand, Elizabeth, Ballard, Clive, Gsteiger, Sandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881030/
https://www.ncbi.nlm.nih.gov/pubmed/36404542
http://dx.doi.org/10.3233/JAD-220471
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author Garcia, Maria João
Leadley, Regina
Lang, Shona
Ross, Janine
Vinand, Elizabeth
Ballard, Clive
Gsteiger, Sandro
author_facet Garcia, Maria João
Leadley, Regina
Lang, Shona
Ross, Janine
Vinand, Elizabeth
Ballard, Clive
Gsteiger, Sandro
author_sort Garcia, Maria João
collection PubMed
description BACKGROUND: Alzheimer’s disease (AD) is the most common type of dementia, causing progressive decline of memory, thinking, and behavior, impairing daily functioning. Early AD (eAD) includes mild cognitive impairment (MCI) due to AD and mild AD dementia. OBJECTIVE: The aim of this study was to investigate symptomatic treatment prevalence and treatment patterns in eAD. METHODS: Embase, MEDLINE, and EBM Reviews were searched in November 2021 for observational studies reporting symptomatic treatment patterns in eAD. The range of patients receiving treatment was collated. Risk of bias was assessed using the Joanna Briggs Institute (JBI) prevalence tool. Two independent reviewers screened the records, one performed data extraction and quality assessment while a second checked. RESULTS: Twenty-one studies (prospective and retrospective cohorts, cross-sectional studies, and a survey) were included. Population size ranged from 23 to 2,028. Worldwide, 18 to 35% of patients diagnosed with MCI due to AD received any AChE inhibitor (three studies; n = 631), 7 to 8% memantine (two studies; n = 229), and 9% combination therapy (one study; n = 402). Patients receiving no treatment ranged from 41 to 54% (two studies; n = 733). Worldwide, in mild AD dementia patients, 13 to 89% received any AChE inhibitor (six studies; n = 3,715), 1 to 21% memantine (five studies, n = 3,527), and 0.4 to 39% combination therapy (four studies, n = 3,018). Patients receiving no treatment ranged from 9 to 26% (five studies, n = 4,073). CONCLUSION: Limitations in reporting led to unclear risk of bias. The results reveal a pattern of use of symptomatic treatment in eAD beyond approved labels and highlights the opportunity for new consensus guidelines to inform clinical practice.
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spelling pubmed-98810302023-02-08 Real-World Use of Symptomatic Treatments in Early Alzheimer’s Disease Garcia, Maria João Leadley, Regina Lang, Shona Ross, Janine Vinand, Elizabeth Ballard, Clive Gsteiger, Sandro J Alzheimers Dis Systematic Review BACKGROUND: Alzheimer’s disease (AD) is the most common type of dementia, causing progressive decline of memory, thinking, and behavior, impairing daily functioning. Early AD (eAD) includes mild cognitive impairment (MCI) due to AD and mild AD dementia. OBJECTIVE: The aim of this study was to investigate symptomatic treatment prevalence and treatment patterns in eAD. METHODS: Embase, MEDLINE, and EBM Reviews were searched in November 2021 for observational studies reporting symptomatic treatment patterns in eAD. The range of patients receiving treatment was collated. Risk of bias was assessed using the Joanna Briggs Institute (JBI) prevalence tool. Two independent reviewers screened the records, one performed data extraction and quality assessment while a second checked. RESULTS: Twenty-one studies (prospective and retrospective cohorts, cross-sectional studies, and a survey) were included. Population size ranged from 23 to 2,028. Worldwide, 18 to 35% of patients diagnosed with MCI due to AD received any AChE inhibitor (three studies; n = 631), 7 to 8% memantine (two studies; n = 229), and 9% combination therapy (one study; n = 402). Patients receiving no treatment ranged from 41 to 54% (two studies; n = 733). Worldwide, in mild AD dementia patients, 13 to 89% received any AChE inhibitor (six studies; n = 3,715), 1 to 21% memantine (five studies, n = 3,527), and 0.4 to 39% combination therapy (four studies, n = 3,018). Patients receiving no treatment ranged from 9 to 26% (five studies, n = 4,073). CONCLUSION: Limitations in reporting led to unclear risk of bias. The results reveal a pattern of use of symptomatic treatment in eAD beyond approved labels and highlights the opportunity for new consensus guidelines to inform clinical practice. IOS Press 2023-01-03 /pmc/articles/PMC9881030/ /pubmed/36404542 http://dx.doi.org/10.3233/JAD-220471 Text en © 2023 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Systematic Review
Garcia, Maria João
Leadley, Regina
Lang, Shona
Ross, Janine
Vinand, Elizabeth
Ballard, Clive
Gsteiger, Sandro
Real-World Use of Symptomatic Treatments in Early Alzheimer’s Disease
title Real-World Use of Symptomatic Treatments in Early Alzheimer’s Disease
title_full Real-World Use of Symptomatic Treatments in Early Alzheimer’s Disease
title_fullStr Real-World Use of Symptomatic Treatments in Early Alzheimer’s Disease
title_full_unstemmed Real-World Use of Symptomatic Treatments in Early Alzheimer’s Disease
title_short Real-World Use of Symptomatic Treatments in Early Alzheimer’s Disease
title_sort real-world use of symptomatic treatments in early alzheimer’s disease
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881030/
https://www.ncbi.nlm.nih.gov/pubmed/36404542
http://dx.doi.org/10.3233/JAD-220471
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