Diagnostic procedures for Parkinson's disease dementia: Recommendations from the movement disorder society task force
Identifieur interne : 002E97 ( Main/Exploration ); précédent : 002E96; suivant : 002E98Diagnostic procedures for Parkinson's disease dementia: Recommendations from the movement disorder society task force
Auteurs : Bruno Dubois [France] ; David Burn [Royaume-Uni] ; Christopher Goetz [États-Unis] ; Dag Aarsland [Norvège] ; Richard G. Brown [Royaume-Uni] ; Gerald A. Broe [Australie] ; Dennis Dickson [États-Unis] ; Charles Duyckaerts [France] ; Jefferey Cummings [États-Unis] ; Serge Gauthier [Canada] ; Amos Korczyn [Israël] ; Andrew Lees (neurologue) [Royaume-Uni] ; Richard Levy [France] ; Irene Litvan [États-Unis] ; Yoshikuni Mizuno [Japon] ; Ian G. Mckeith [Royaume-Uni] ; C. Warren Olanow [États-Unis] ; Werner Poewe [Autriche] ; Cristina Sampaio [Portugal] ; Eduardo Tolosa [Espagne] ; Murat Emre [Turquie]Source :
- Movement Disorders [ 0885-3185 ] ; 2007-12-15.
English descriptors
- KwdEn :
- Activities of Daily Living, Cognition Disorders (etiology), Cognition Disorders (psychology), Dementia (diagnosis), Dementia (etiology), Dementia (psychology), Humans, Memory Disorders (etiology), Memory Disorders (psychology), PD dementia, Parkinson Disease (complications), Parkinson Disease (psychology), Parkinson's disease, Psychomotor Performance (physiology), diagnostic criteria, executive functions, task force.
- MESH :
- complications : Parkinson Disease.
- diagnosis : Dementia.
- etiology : Cognition Disorders, Dementia, Memory Disorders.
- physiology : Psychomotor Performance.
- psychology : Cognition Disorders, Dementia, Memory Disorders, Parkinson Disease.
- Activities of Daily Living, Humans.
Abstract
A preceding article described the clinical features of Parkinson's disease dementia (PD‐D) and proposed clinical diagnostic criteria for “probable” and “possible” PD‐D. The main focus of this article is to operationalize the diagnosis of PD‐D and to propose pratical guidelines based on a two level process depending upon the clinical scenario and the expertise of the evaluator involved in the assessment. Level I is aimed primarily at the clinician with no particular expertise in neuropsychological methods, but who requires a simple, pragmatic set of tests that are not excessively time‐consuming. Level I can be used alone or in concert with Level II, which is more suitable when there is the need to specify the pattern and the severity on the dementia of PD‐D for clinical monitoring, research studies or pharmacological trials. Level II tests can also be proposed when the diagnosis of PD‐D remains uncertain or equivocal at the end of a Level I evaluation. Given the lack of evidence‐based standards for some tests when applied in this clinical context, we have tried to make practical and unambiguous recommendations, based upon the available literature and the collective experience of the Task Force. We accept, however, that further validation of certain tests and modifications in the recommended cut off values will be required through future studies. © 2007 Movement Disorder Society
Url:
DOI: 10.1002/mds.21844
Affiliations:
- Australie, Autriche, Canada, Espagne, France, Israël, Japon, Norvège, Portugal, Royaume-Uni, Turquie, États-Unis
- Angleterre, Californie, Floride, Grand Londres, Illinois, Kentucky, Tyrol (Land), État de New York
- Innsbruck, Londres, Paris, Tokyo
- National Hospital for Neurology and Neurosurgery, Université de médecine d'Innsbruck
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Le document en format XML
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<front><div type="abstract" xml:lang="en">A preceding article described the clinical features of Parkinson's disease dementia (PD‐D) and proposed clinical diagnostic criteria for “probable” and “possible” PD‐D. The main focus of this article is to operationalize the diagnosis of PD‐D and to propose pratical guidelines based on a two level process depending upon the clinical scenario and the expertise of the evaluator involved in the assessment. Level I is aimed primarily at the clinician with no particular expertise in neuropsychological methods, but who requires a simple, pragmatic set of tests that are not excessively time‐consuming. Level I can be used alone or in concert with Level II, which is more suitable when there is the need to specify the pattern and the severity on the dementia of PD‐D for clinical monitoring, research studies or pharmacological trials. Level II tests can also be proposed when the diagnosis of PD‐D remains uncertain or equivocal at the end of a Level I evaluation. Given the lack of evidence‐based standards for some tests when applied in this clinical context, we have tried to make practical and unambiguous recommendations, based upon the available literature and the collective experience of the Task Force. We accept, however, that further validation of certain tests and modifications in the recommended cut off values will be required through future studies. © 2007 Movement Disorder Society</div>
</front>
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