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Validation of the short version of the 10/66 dementia diagnosis in multiethnic Asian older adults in Singapore
BACKGROUND: To validate the short version of the 10/66 dementia diagnosis against the standard version of the 10/66 dementia diagnosis and clinical diagnosis and examine concurrent validity with the World Health Organisation Disability Assessment schedule and care needs in a multiethnic Asian older...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399400/ https://www.ncbi.nlm.nih.gov/pubmed/28431511 http://dx.doi.org/10.1186/s12877-017-0475-7 |
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author | Abdin, Edimansyah Vaingankar, Janhavi Ajit Picco, Louisa Chua, Boon Yiang Prince, Martin Chong, Siow Ann Subramaniam, Mythily |
author_facet | Abdin, Edimansyah Vaingankar, Janhavi Ajit Picco, Louisa Chua, Boon Yiang Prince, Martin Chong, Siow Ann Subramaniam, Mythily |
author_sort | Abdin, Edimansyah |
collection | PubMed |
description | BACKGROUND: To validate the short version of the 10/66 dementia diagnosis against the standard version of the 10/66 dementia diagnosis and clinical diagnosis and examine concurrent validity with the World Health Organisation Disability Assessment schedule and care needs in a multiethnic Asian older adult population in Singapore. METHODS: Data from the Well-being of the Singapore Elderly study, a nationally representative survey of the older Singapore Resident population aged 60 years and above was used. The validity of the short version of the 10/66 dementia diagnostic criteria derived from the Community Screening Instrument for Dementia, the modified Consortium to Establish a Registry of Alzheimer’s Disease 10-word list delayed recall and the EURO-D depression screen were examined against the standard version of the 10/66 dementia diagnosis and clinician diagnosis as a gold standard. Concurrent validity was tested by examining the relationships between the short version 10/66 dementia diagnosis, disability and care needs. RESULTS: A total of 2373 respondents who had completed data on the short version diagnosis were included in this study. The majority (82.63%) of respondents were of Chinese descent, 9.86% were Malays, 6.12% were of Indian descent and 1.39% belonged to other ethnic group. We found the short version 10/66 dementia diagnosis showed almost perfect agreement with the standard version 10/66 dementia diagnosis (kappa = 0.90, AUC = 0.96) and substantial agreement with clinical diagnosis (kappa = 0.70, AUC = 0.87). The weighted prevalence of dementia in the population was slightly higher based on the short version diagnosis than the standard version diagnosis (10.74% vs. 10.04%). We also found that those with the short version 10/66 dementia were significantly associated with higher disability (β = 28.90, 95% CI = 23.62, 9.62) and needed care occasionally (OR =35.21, 95% CI = 18.08, 68.59) or much of the time (OR = 9.02, 95% CI = 5.21, 15.61). CONCLUSIONS: The study found that the short version 10/66 dementia diagnosis has excellent validity to diagnose dementia in a multiethnic Asian population in Singapore. Further research is required to determine the usefulness of this diagnosis in clinical practice or institutional settings to aid early detection and intervention for dementia. |
format | Online Article Text |
id | pubmed-5399400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53994002017-04-24 Validation of the short version of the 10/66 dementia diagnosis in multiethnic Asian older adults in Singapore Abdin, Edimansyah Vaingankar, Janhavi Ajit Picco, Louisa Chua, Boon Yiang Prince, Martin Chong, Siow Ann Subramaniam, Mythily BMC Geriatr Research Article BACKGROUND: To validate the short version of the 10/66 dementia diagnosis against the standard version of the 10/66 dementia diagnosis and clinical diagnosis and examine concurrent validity with the World Health Organisation Disability Assessment schedule and care needs in a multiethnic Asian older adult population in Singapore. METHODS: Data from the Well-being of the Singapore Elderly study, a nationally representative survey of the older Singapore Resident population aged 60 years and above was used. The validity of the short version of the 10/66 dementia diagnostic criteria derived from the Community Screening Instrument for Dementia, the modified Consortium to Establish a Registry of Alzheimer’s Disease 10-word list delayed recall and the EURO-D depression screen were examined against the standard version of the 10/66 dementia diagnosis and clinician diagnosis as a gold standard. Concurrent validity was tested by examining the relationships between the short version 10/66 dementia diagnosis, disability and care needs. RESULTS: A total of 2373 respondents who had completed data on the short version diagnosis were included in this study. The majority (82.63%) of respondents were of Chinese descent, 9.86% were Malays, 6.12% were of Indian descent and 1.39% belonged to other ethnic group. We found the short version 10/66 dementia diagnosis showed almost perfect agreement with the standard version 10/66 dementia diagnosis (kappa = 0.90, AUC = 0.96) and substantial agreement with clinical diagnosis (kappa = 0.70, AUC = 0.87). The weighted prevalence of dementia in the population was slightly higher based on the short version diagnosis than the standard version diagnosis (10.74% vs. 10.04%). We also found that those with the short version 10/66 dementia were significantly associated with higher disability (β = 28.90, 95% CI = 23.62, 9.62) and needed care occasionally (OR =35.21, 95% CI = 18.08, 68.59) or much of the time (OR = 9.02, 95% CI = 5.21, 15.61). CONCLUSIONS: The study found that the short version 10/66 dementia diagnosis has excellent validity to diagnose dementia in a multiethnic Asian population in Singapore. Further research is required to determine the usefulness of this diagnosis in clinical practice or institutional settings to aid early detection and intervention for dementia. BioMed Central 2017-04-21 /pmc/articles/PMC5399400/ /pubmed/28431511 http://dx.doi.org/10.1186/s12877-017-0475-7 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Abdin, Edimansyah Vaingankar, Janhavi Ajit Picco, Louisa Chua, Boon Yiang Prince, Martin Chong, Siow Ann Subramaniam, Mythily Validation of the short version of the 10/66 dementia diagnosis in multiethnic Asian older adults in Singapore |
title | Validation of the short version of the 10/66 dementia diagnosis in multiethnic Asian older adults in Singapore |
title_full | Validation of the short version of the 10/66 dementia diagnosis in multiethnic Asian older adults in Singapore |
title_fullStr | Validation of the short version of the 10/66 dementia diagnosis in multiethnic Asian older adults in Singapore |
title_full_unstemmed | Validation of the short version of the 10/66 dementia diagnosis in multiethnic Asian older adults in Singapore |
title_short | Validation of the short version of the 10/66 dementia diagnosis in multiethnic Asian older adults in Singapore |
title_sort | validation of the short version of the 10/66 dementia diagnosis in multiethnic asian older adults in singapore |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399400/ https://www.ncbi.nlm.nih.gov/pubmed/28431511 http://dx.doi.org/10.1186/s12877-017-0475-7 |
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