2019
DOI: 10.1016/j.jamda.2019.02.004
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The Optimal Short Version of Montreal Cognitive Assessment in Diagnosing Mild Cognitive Impairment and Dementia

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Cited by 21 publications
(29 citation statements)
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“…The apparently normal cognition during the initial evaluations may not be sufficient to exclude underlying neurodegenerative processes, and there remains a need for continued and close surveillance to detect the onset of cognitive decline in this group of individuals. The findings may have implications to the future diagnostic criteria of late-life psychotic disorders, suggesting the need for greater clarity on the extent of clinical investigations in the diagnostic criteriasuch as specifying the need for repeated administration of a neuropsychological battery (or in its absence, another briefer but sensitive cognitive test such as the Montreal Cognitive Assessment) [27,28,62,63]-before a diagnosis of late-life psychotic disorder can be accurately made. Potentially, the future diagnostic criteria of late-life psychotic disorders may also incorporate the newer biomarkers of dementia (such as those related to amyloid protein, tau protein, and neuronal injury) [10] to definitively exclude underlying neurodegenerative processes, especially when these biomarkers become more accessible to general clinicians in the foreseeable future.…”
Section: Potential Implications Of the Findingsmentioning
confidence: 99%
“…The apparently normal cognition during the initial evaluations may not be sufficient to exclude underlying neurodegenerative processes, and there remains a need for continued and close surveillance to detect the onset of cognitive decline in this group of individuals. The findings may have implications to the future diagnostic criteria of late-life psychotic disorders, suggesting the need for greater clarity on the extent of clinical investigations in the diagnostic criteriasuch as specifying the need for repeated administration of a neuropsychological battery (or in its absence, another briefer but sensitive cognitive test such as the Montreal Cognitive Assessment) [27,28,62,63]-before a diagnosis of late-life psychotic disorder can be accurately made. Potentially, the future diagnostic criteria of late-life psychotic disorders may also incorporate the newer biomarkers of dementia (such as those related to amyloid protein, tau protein, and neuronal injury) [10] to definitively exclude underlying neurodegenerative processes, especially when these biomarkers become more accessible to general clinicians in the foreseeable future.…”
Section: Potential Implications Of the Findingsmentioning
confidence: 99%
“…Compared to other instruments available for MCI and early dementia diagnosis, for example CERAD and MoCA, accuracy for CAB seems to be worse. The original MoCA version has an AUC of 0.893 and the shorter MoCA versions by Roal et al and Wong et al demonstrated comparable AUC values of 88.4-88.9% (134,147,148). CERAD had an excellent AUC in one longitudinal PHC population but the result needs to be revalidated (91).…”
Section: Cognitive Assessment Batterymentioning
confidence: 97%
“…One modern example is the cognitive instrument MoCA, which in recent years has been introduced as a possible alternative, especially for detection of MCI and early dementia (77). Short versions of MoCA applicable for PHC has also been studied as an alternative (134). We do have normative values of MoCA results in Sweden but worldwide PHC data are scarce (76).…”
Section: Papermentioning
confidence: 99%
“…In general, AUC > 0.9 is deemed to be excellent performance [50] and indicates that a strategy has a low error rate (<10%) and is suitable for case-finding purposes. AUC was also compared among the three strategies via a non-parametric approach proposed by DeLong et al [20,21,31,[51][52][53] with statistically significant differences defined as P ≤ 0.05 and clinically significant differences defined as AUC differences of ≥1% (when a test is used for case finding in a large population of one million people, a 1% difference in AUC would have translated into an additional 10 000 people being misclassified) [21].…”
Section: Statistical Analysesmentioning
confidence: 99%
“…Conventionally, three strategies can be employed in the case finding of dementia, i.e. using informant reports alone [such as AD8 and Functional Activities Questionnaire (FAQ)] [17,18], brief cognitive tests alone [such as Mini-Cog and short variants of Montreal Cognitive Assessment (MoCA)] [19][20][21][22] and combined measures that pair informant reports with brief cognitive tests [23][24][25][26][27][28][29]. Each case-finding strategy has inherent strengths and limitations, with the literature remaining unclear on the right strategy to adopt across different healthcare services with varying clinical resources and patient profiles.…”
Section: Introductionmentioning
confidence: 99%