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

被引:6
作者
Cova, Ilaria [1 ]
Mele, Francesco [1 ]
Zerini, Federica [2 ]
Maggiore, Laura [1 ]
Rosa, Silvia [1 ]
Cucumo, Valentina [1 ]
Brambilla, Michela [1 ]
Nicotra, Alessia [1 ]
Maestri, Giorgia [1 ]
Bertora, Pierluigi [1 ,2 ]
Pomati, Simone [1 ]
Pantoni, Leonardo [1 ,2 ]
机构
[1] Luigi Sacco Univ Hosp, Neurol Unit, Milan, Italy
[2] Univ Milan, Luigi Sacco Dept Biomed & Clin Sci, Stroke & Dementia Lab, Via Giovanni Battista Grassi 74, I-20157 Milan, Italy
关键词
Stroke; Post-stroke cognitive impairment; Post-stroke dementia; Clock Drawing Test; Predictivity; NATIONAL INSTITUTE; RATING-SCALE; IMPAIRMENT; GUIDELINES; ILLNESS; VERSION; TOOLS; MOOD; MOCA; MRI;
D O I
10.1007/s00415-021-10637-z
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 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 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 A bedside cognitive screening with the CDT helps identifying patients at higher risk of PSCI.
引用
收藏
页码:342 / 349
页数:8
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