2011
DOI: 10.1080/13607863.2010.508769
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Development of a dementia assessment quality database

Abstract: Clinical quality indicators based on all patients evaluated for dementia can be used to standardize and harmonize the evaluation process and improve clinical health services.

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Cited by 14 publications
(11 citation statements)
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References 16 publications
(16 reference statements)
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“…However, the specialist care units, where patients are visited by geriatricians and/or neurologists and/or psychiatrists, followed the guidelines to a significantly higher extent than primary care units. The use of a structural brain scan (CT or MRI) in Denmark has been reported to be as high as 93% [23], which is similar to the percentage reported in the present study.…”
Section: Discussionsupporting
confidence: 82%
“…However, the specialist care units, where patients are visited by geriatricians and/or neurologists and/or psychiatrists, followed the guidelines to a significantly higher extent than primary care units. The use of a structural brain scan (CT or MRI) in Denmark has been reported to be as high as 93% [23], which is similar to the percentage reported in the present study.…”
Section: Discussionsupporting
confidence: 82%
“…AD and related disorders databases already exist in several countries. Although the BNA provides a minimum dataset in comparison with others containing biological [19], histological [20,21], or clinical data [22,23], its advantage is of course its size and statistical power. With the example of the French Hospital Database on HIV [24], the BNA is one of the rare national databases allowing the ongoing collection of socio-demographic, epidemiological, and clinical data on AD and related disorders.…”
Section: Discussionmentioning
confidence: 99%
“…There have been similar successful attempts in other countries to establish a quality dementia registry, such as in Denmark [ 12 ]. Whereas other registries have been developed to facilitate epidemiological studies [ 13 ], study the clinical expression of AD [ 14 ], provide a framework for recruitment of patients for clinical trials [ 15 ] or promote equality in the access for medical services [ 16 ].…”
Section: Discussionmentioning
confidence: 99%