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Domain-specific versus generalized cognitive screening in acute stroke
Cognitive assessments after stroke are typically short form tests developed for dementia that generates pass/fail classifications (e.g. the MoCA). The Oxford Cognitive Screen (OCS) provides a domain-specific cognitive profile designed for stroke survivors. This study compared the use of the MoCA and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751179/ https://www.ncbi.nlm.nih.gov/pubmed/26588918 http://dx.doi.org/10.1007/s00415-015-7964-4 |
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author | Demeyere, Nele Riddoch, M. J. Slavkova, E. D. Jones, K. Reckless, I. Mathieson, P. Humphreys, G. W. |
author_facet | Demeyere, Nele Riddoch, M. J. Slavkova, E. D. Jones, K. Reckless, I. Mathieson, P. Humphreys, G. W. |
author_sort | Demeyere, Nele |
collection | PubMed |
description | Cognitive assessments after stroke are typically short form tests developed for dementia that generates pass/fail classifications (e.g. the MoCA). The Oxford Cognitive Screen (OCS) provides a domain-specific cognitive profile designed for stroke survivors. This study compared the use of the MoCA and the OCS in acute stroke with respect to symptom specificity and aspects of clinical utility. A cross-sectional study with a consecutive sample of 200 stroke patients within 3 weeks of stroke completing MoCA and OCS. Demographic data, lesion side and Barthel scores were recorded. Inclusivity was assessed in terms of completion rates and reasons for non-completion were evaluated. The incidence of cognitive impairments on both the MoCA and OCS sub-domains was calculated and differences in stroke specificity, cognitive profiles and independence of the measures were addressed. The incidence of acute cognitive impairment was high: 76 % of patients were impaired on MoCA, and 86 % demonstrated at least one impairment on the cognitive domains assessed in the OCS. OCS was more sensitive than MoCA overall (87 vs 78 % sensitivity) and OCS alone provided domain-specific information on prevalent post-stroke cognitive impairments (neglect, apraxia and reading/writing ability). Unlike the MOCA, the OCS was not dominated by left hemisphere impairments but gave differentiated profiles across the contrasting domains. The OCS detects important cognitive deficits after stroke not assessed in the MoCA, it is inclusive for patients with aphasia and neglect and it is less confounded by co-occurring difficulties in these domains. |
format | Online Article Text |
id | pubmed-4751179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-47511792016-02-22 Domain-specific versus generalized cognitive screening in acute stroke Demeyere, Nele Riddoch, M. J. Slavkova, E. D. Jones, K. Reckless, I. Mathieson, P. Humphreys, G. W. J Neurol Original Communication Cognitive assessments after stroke are typically short form tests developed for dementia that generates pass/fail classifications (e.g. the MoCA). The Oxford Cognitive Screen (OCS) provides a domain-specific cognitive profile designed for stroke survivors. This study compared the use of the MoCA and the OCS in acute stroke with respect to symptom specificity and aspects of clinical utility. A cross-sectional study with a consecutive sample of 200 stroke patients within 3 weeks of stroke completing MoCA and OCS. Demographic data, lesion side and Barthel scores were recorded. Inclusivity was assessed in terms of completion rates and reasons for non-completion were evaluated. The incidence of cognitive impairments on both the MoCA and OCS sub-domains was calculated and differences in stroke specificity, cognitive profiles and independence of the measures were addressed. The incidence of acute cognitive impairment was high: 76 % of patients were impaired on MoCA, and 86 % demonstrated at least one impairment on the cognitive domains assessed in the OCS. OCS was more sensitive than MoCA overall (87 vs 78 % sensitivity) and OCS alone provided domain-specific information on prevalent post-stroke cognitive impairments (neglect, apraxia and reading/writing ability). Unlike the MOCA, the OCS was not dominated by left hemisphere impairments but gave differentiated profiles across the contrasting domains. The OCS detects important cognitive deficits after stroke not assessed in the MoCA, it is inclusive for patients with aphasia and neglect and it is less confounded by co-occurring difficulties in these domains. Springer Berlin Heidelberg 2015-11-20 2016 /pmc/articles/PMC4751179/ /pubmed/26588918 http://dx.doi.org/10.1007/s00415-015-7964-4 Text en © The Author(s) 2015 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. |
spellingShingle | Original Communication Demeyere, Nele Riddoch, M. J. Slavkova, E. D. Jones, K. Reckless, I. Mathieson, P. Humphreys, G. W. Domain-specific versus generalized cognitive screening in acute stroke |
title | Domain-specific versus generalized cognitive screening in acute stroke |
title_full | Domain-specific versus generalized cognitive screening in acute stroke |
title_fullStr | Domain-specific versus generalized cognitive screening in acute stroke |
title_full_unstemmed | Domain-specific versus generalized cognitive screening in acute stroke |
title_short | Domain-specific versus generalized cognitive screening in acute stroke |
title_sort | domain-specific versus generalized cognitive screening in acute stroke |
topic | Original Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751179/ https://www.ncbi.nlm.nih.gov/pubmed/26588918 http://dx.doi.org/10.1007/s00415-015-7964-4 |
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