The Clock Drawing Test as a predictor of cognitive decline in non-demented stroke patients.

Clock Drawing Test Post-stroke cognitive impairment Post-stroke dementia Predictivity Stroke

Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
Jan 2022
Historique:
received: 15 04 2021
accepted: 31 05 2021
revised: 28 05 2021
pubmed: 8 6 2021
medline: 11 1 2022
entrez: 7 6 2021
Statut: ppublish

Résumé

The early detection of patients at risk of post-stroke cognitive impairment (PSCI) may help planning subacute and long-term care. We aimed to determine the predictivity of two screening cognitive tests on the occurrence of mild cognitive impairment or dementia in acute stroke patients. A cognitive assessment within a few days of ischemic or hemorrhagic stroke was performed in patients consecutively admitted to a stroke unit over 14 months by means of the Clock Drawing Test (CDT) and the Montreal Cognitive Assessment-Basic (MoCA-B). Out of 191 stroke survivors who were non-demented at baseline, 168 attended at least one follow-up visit. At follow-up (mean duration ± SD 12.8 ± 8.7 months), 28 (18.9%) incident cases of MCI and 27 (18%) cases of dementia were recorded. In comparison with patients who remained cognitively stable at follow-up, these patients were older, less educated, had more comorbidities, a higher score on the National Institutes of Health Stroke Scale (NIHSS) at admission, more severe cerebral atrophy, and lower MoCA-B and CDT scores at baseline. In multi-adjusted (for age, education, comorbidities score, NIHSS at admission and atrophy score) model, a pathological score on baseline CDT (< 6.55) was associated with a higher risk of PSCI at follow-up (HR 2.022; 95% CI 1.025-3.989, p < 0.05) with respect to non-pathological scores. A pathological baseline score on MoCA-B (< 24) did not predict increased risk of cognitive decline at follow-up nor increased predictivity of stand-alone CDT. A bedside cognitive screening with the CDT helps identifying patients at higher risk of PSCI.

Sections du résumé

BACKGROUND BACKGROUND
The early detection of patients at risk of post-stroke cognitive impairment (PSCI) may help planning subacute and long-term care. We aimed to determine the predictivity of two screening cognitive tests on the occurrence of mild cognitive impairment or dementia in acute stroke patients.
METHODS METHODS
A cognitive assessment within a few days of ischemic or hemorrhagic stroke was performed in patients consecutively admitted to a stroke unit over 14 months by means of the Clock Drawing Test (CDT) and the Montreal Cognitive Assessment-Basic (MoCA-B).
RESULTS RESULTS
Out of 191 stroke survivors who were non-demented at baseline, 168 attended at least one follow-up visit. At follow-up (mean duration ± SD 12.8 ± 8.7 months), 28 (18.9%) incident cases of MCI and 27 (18%) cases of dementia were recorded. In comparison with patients who remained cognitively stable at follow-up, these patients were older, less educated, had more comorbidities, a higher score on the National Institutes of Health Stroke Scale (NIHSS) at admission, more severe cerebral atrophy, and lower MoCA-B and CDT scores at baseline. In multi-adjusted (for age, education, comorbidities score, NIHSS at admission and atrophy score) model, a pathological score on baseline CDT (< 6.55) was associated with a higher risk of PSCI at follow-up (HR 2.022; 95% CI 1.025-3.989, p < 0.05) with respect to non-pathological scores. A pathological baseline score on MoCA-B (< 24) did not predict increased risk of cognitive decline at follow-up nor increased predictivity of stand-alone CDT.
CONCLUSION CONCLUSIONS
A bedside cognitive screening with the CDT helps identifying patients at higher risk of PSCI.

Identifiants

pubmed: 34095964
doi: 10.1007/s00415-021-10637-z
pii: 10.1007/s00415-021-10637-z
pmc: PMC8739305
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

342-349

Informations de copyright

© 2021. The Author(s).

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Auteurs

Ilaria Cova (I)

Neurology Unit, Luigi Sacco University Hospital, Milan, Italy.

Francesco Mele (F)

Neurology Unit, Luigi Sacco University Hospital, Milan, Italy.

Federica Zerini (F)

Stroke and Dementia Lab, "Luigi Sacco" Department of Biomedical and Clinical Sciences, University of Milan, Via Giovanni Battista Grassi 74, 20157, Milan, Italy.

Laura Maggiore (L)

Neurology Unit, Luigi Sacco University Hospital, Milan, Italy.

Silvia Rosa (S)

Neurology Unit, Luigi Sacco University Hospital, Milan, Italy.

Valentina Cucumo (V)

Neurology Unit, Luigi Sacco University Hospital, Milan, Italy.

Michela Brambilla (M)

Neurology Unit, Luigi Sacco University Hospital, Milan, Italy.

Alessia Nicotra (A)

Neurology Unit, Luigi Sacco University Hospital, Milan, Italy.

Giorgia Maestri (G)

Neurology Unit, Luigi Sacco University Hospital, Milan, Italy.

Pierluigi Bertora (P)

Neurology Unit, Luigi Sacco University Hospital, Milan, Italy.
Stroke and Dementia Lab, "Luigi Sacco" Department of Biomedical and Clinical Sciences, University of Milan, Via Giovanni Battista Grassi 74, 20157, Milan, Italy.

Simone Pomati (S)

Neurology Unit, Luigi Sacco University Hospital, Milan, Italy.

Leonardo Pantoni (L)

Neurology Unit, Luigi Sacco University Hospital, Milan, Italy. leonardo.pantoni@unimi.it.
Stroke and Dementia Lab, "Luigi Sacco" Department of Biomedical and Clinical Sciences, University of Milan, Via Giovanni Battista Grassi 74, 20157, Milan, Italy. leonardo.pantoni@unimi.it.

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