La maladie de Parkinson au Canada (serveur d'exploration)

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Diagnosis and management of Parkinson's disease dementia

Identifieur interne : 000626 ( PascalFrancis/Corpus ); précédent : 000625; suivant : 000627

Diagnosis and management of Parkinson's disease dementia

Auteurs : W. Poewe ; S. Gauthier ; D. Aarsland ; J. B. Leverenz ; P. Barone ; D. Weintraub ; E. Tolosa ; B. Dubois

Source :

RBID : Pascal:08-0445025

Descripteurs français

English descriptors

Abstract

Parkinson's disease (PD) has long been considered predominantly a motor disorder. However, its frequent association with dementia, which contributes significantly to the morbidity and mortality of the condition, is gaining increasing recognition. PD dementia (PDD) has a unique clinical profile and neuropathology, distinct from Alzheimer's disease (AD). Cholinergic deficits, a feature of both AD and PDD, underlie the rationale for cholinesterase inhibitor therapy in both conditions. In clinical practice, it is important that PDD should be recognised and appropriately treated. This review aims to outline the recently proposed clinical diagnostic criteria for PDD and to summarise the guidelines/recommendations published since 2006 on the use of cholinesterase inhibitors in the management of PDD. Although the cholinesterase inhibitor rivastigmine has recently been approved for the management of PDD, there remains a need for the development of novel therapies that can affect key mechanisms of the disease or prevent/delay patients with PD and mild cognitive impairment from progressing to PDD.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 1368-5031
A03   1    @0 Int. j. clin. pract. : (Esher)
A05       @2 62
A06       @2 10
A08 01  1  ENG  @1 Diagnosis and management of Parkinson's disease dementia
A11 01  1    @1 POEWE (W.)
A11 02  1    @1 GAUTHIER (S.)
A11 03  1    @1 AARSLAND (D.)
A11 04  1    @1 LEVERENZ (J. B.)
A11 05  1    @1 BARONE (P.)
A11 06  1    @1 WEINTRAUB (D.)
A11 07  1    @1 TOLOSA (E.)
A11 08  1    @1 DUBOIS (B.)
A14 01      @1 Department of Neurology, Medical University Innsbruck @2 Innsbruck @3 AUT @Z 1 aut.
A14 02      @1 Alzheimer's Disease Research Unit, McGill Centre for Studies in Aging, Douglas Mental Health University Institute @2 Montréal, QC @3 CAN @Z 2 aut.
A14 03      @1 Norweigen Centre for Movement Disorders, Stavenger University Hospital @2 Stavenger @3 NOR @Z 3 aut.
A14 04      @1 Institute of Clinical Medicine, University of Bergen @2 Bergen @3 NOR @Z 3 aut.
A14 05      @1 Mental Illness and Parkinson's Disease Research Education and Clinical Centers, VA-PSHCS, and Departments of Neurology and Psychiatry and Behavioral Sciences, University of Washington @2 Seattle, WA @3 USA @Z 4 aut.
A14 06      @1 Dipartimento di Scienze Neurologiche, Università Federico II di Napoli @2 Naples @3 ITA @Z 5 aut.
A14 07      @1 Department of Psychiatry, University of Pennsylvania @2 Philadelphia, PA @3 USA @Z 6 aut.
A14 08      @1 Parkinson's Disease and Movement Disorders Unit, Institut Clinic de Neurociencies, and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Hospital Clinic de Barcelona, Institut d'lnvestigacions Biomèdiques August Pi i Sunyer, Universitat de Barcelona @2 Barcelona @3 ESP @Z 7 aut.
A14 09      @1 INSERM.UPMC UMRS 610, Federation of Neurology, Salpêtrière Hospital; University of Paris @2 Paris @3 FRA @Z 8 aut.
A20       @1 1581-1587
A21       @1 2008
A23 01      @0 ENG
A43 01      @1 INIST @2 15561 @5 354000185233900160
A44       @0 0000 @1 © 2008 INIST-CNRS. All rights reserved.
A45       @0 47 ref.
A47 01  1    @0 08-0445025
A60       @1 P
A61       @0 A
A64 01  1    @0 International journal of clinical practice : (Esher)
A66 01      @0 GBR
C01 01    ENG  @0 Parkinson's disease (PD) has long been considered predominantly a motor disorder. However, its frequent association with dementia, which contributes significantly to the morbidity and mortality of the condition, is gaining increasing recognition. PD dementia (PDD) has a unique clinical profile and neuropathology, distinct from Alzheimer's disease (AD). Cholinergic deficits, a feature of both AD and PDD, underlie the rationale for cholinesterase inhibitor therapy in both conditions. In clinical practice, it is important that PDD should be recognised and appropriately treated. This review aims to outline the recently proposed clinical diagnostic criteria for PDD and to summarise the guidelines/recommendations published since 2006 on the use of cholinesterase inhibitors in the management of PDD. Although the cholinesterase inhibitor rivastigmine has recently been approved for the management of PDD, there remains a need for the development of novel therapies that can affect key mechanisms of the disease or prevent/delay patients with PD and mild cognitive impairment from progressing to PDD.
C02 01  X    @0 002B01
C02 02  X    @0 002B17G
C03 01  X  FRE  @0 Maladie de Parkinson @2 NM @5 01
C03 01  X  ENG  @0 Parkinson disease @2 NM @5 01
C03 01  X  SPA  @0 Parkinson enfermedad @2 NM @5 01
C03 02  X  FRE  @0 Diagnostic @5 02
C03 02  X  ENG  @0 Diagnosis @5 02
C03 02  X  SPA  @0 Diagnóstico @5 02
C03 03  X  FRE  @0 Conduite à tenir @5 03
C03 03  X  ENG  @0 Clinical management @5 03
C03 03  X  SPA  @0 Actitud médica @5 03
C03 04  X  FRE  @0 Démence @5 04
C03 04  X  ENG  @0 Dementia @5 04
C03 04  X  SPA  @0 Demencia @5 04
C03 05  X  FRE  @0 Médecine @5 05
C03 05  X  ENG  @0 Medicine @5 05
C03 05  X  SPA  @0 Medicina @5 05
C07 01  X  FRE  @0 Pathologie de l'encéphale @5 37
C07 01  X  ENG  @0 Cerebral disorder @5 37
C07 01  X  SPA  @0 Encéfalo patología @5 37
C07 02  X  FRE  @0 Syndrome extrapyramidal @5 38
C07 02  X  ENG  @0 Extrapyramidal syndrome @5 38
C07 02  X  SPA  @0 Extrapiramidal síndrome @5 38
C07 03  X  FRE  @0 Maladie dégénérative @5 39
C07 03  X  ENG  @0 Degenerative disease @5 39
C07 03  X  SPA  @0 Enfermedad degenerativa @5 39
C07 04  X  FRE  @0 Pathologie du système nerveux central @5 40
C07 04  X  ENG  @0 Central nervous system disease @5 40
C07 04  X  SPA  @0 Sistema nervosio central patología @5 40
C07 05  X  FRE  @0 Pathologie du système nerveux @5 41
C07 05  X  ENG  @0 Nervous system diseases @5 41
C07 05  X  SPA  @0 Sistema nervioso patología @5 41
N21       @1 287
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 08-0445025 INIST
ET : Diagnosis and management of Parkinson's disease dementia
AU : POEWE (W.); GAUTHIER (S.); AARSLAND (D.); LEVERENZ (J. B.); BARONE (P.); WEINTRAUB (D.); TOLOSA (E.); DUBOIS (B.)
AF : Department of Neurology, Medical University Innsbruck/Innsbruck/Autriche (1 aut.); Alzheimer's Disease Research Unit, McGill Centre for Studies in Aging, Douglas Mental Health University Institute/Montréal, QC/Canada (2 aut.); Norweigen Centre for Movement Disorders, Stavenger University Hospital/Stavenger/Norvège (3 aut.); Institute of Clinical Medicine, University of Bergen/Bergen/Norvège (3 aut.); Mental Illness and Parkinson's Disease Research Education and Clinical Centers, VA-PSHCS, and Departments of Neurology and Psychiatry and Behavioral Sciences, University of Washington/Seattle, WA/Etats-Unis (4 aut.); Dipartimento di Scienze Neurologiche, Università Federico II di Napoli/Naples/Italie (5 aut.); Department of Psychiatry, University of Pennsylvania/Philadelphia, PA/Etats-Unis (6 aut.); Parkinson's Disease and Movement Disorders Unit, Institut Clinic de Neurociencies, and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Hospital Clinic de Barcelona, Institut d'lnvestigacions Biomèdiques August Pi i Sunyer, Universitat de Barcelona/Barcelona/Espagne (7 aut.); INSERM.UPMC UMRS 610, Federation of Neurology, Salpêtrière Hospital; University of Paris/Paris/France (8 aut.)
DT : Publication en série; Niveau analytique
SO : International journal of clinical practice : (Esher); ISSN 1368-5031; Royaume-Uni; Da. 2008; Vol. 62; No. 10; Pp. 1581-1587; Bibl. 47 ref.
LA : Anglais
EA : Parkinson's disease (PD) has long been considered predominantly a motor disorder. However, its frequent association with dementia, which contributes significantly to the morbidity and mortality of the condition, is gaining increasing recognition. PD dementia (PDD) has a unique clinical profile and neuropathology, distinct from Alzheimer's disease (AD). Cholinergic deficits, a feature of both AD and PDD, underlie the rationale for cholinesterase inhibitor therapy in both conditions. In clinical practice, it is important that PDD should be recognised and appropriately treated. This review aims to outline the recently proposed clinical diagnostic criteria for PDD and to summarise the guidelines/recommendations published since 2006 on the use of cholinesterase inhibitors in the management of PDD. Although the cholinesterase inhibitor rivastigmine has recently been approved for the management of PDD, there remains a need for the development of novel therapies that can affect key mechanisms of the disease or prevent/delay patients with PD and mild cognitive impairment from progressing to PDD.
CC : 002B01; 002B17G
FD : Maladie de Parkinson; Diagnostic; Conduite à tenir; Démence; Médecine
FG : Pathologie de l'encéphale; Syndrome extrapyramidal; Maladie dégénérative; Pathologie du système nerveux central; Pathologie du système nerveux
ED : Parkinson disease; Diagnosis; Clinical management; Dementia; Medicine
EG : Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease; Nervous system diseases
SD : Parkinson enfermedad; Diagnóstico; Actitud médica; Demencia; Medicina
LO : INIST-15561.354000185233900160
ID : 08-0445025

Links to Exploration step

Pascal:08-0445025

Le document en format XML

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<div type="abstract" xml:lang="en">Parkinson's disease (PD) has long been considered predominantly a motor disorder. However, its frequent association with dementia, which contributes significantly to the morbidity and mortality of the condition, is gaining increasing recognition. PD dementia (PDD) has a unique clinical profile and neuropathology, distinct from Alzheimer's disease (AD). Cholinergic deficits, a feature of both AD and PDD, underlie the rationale for cholinesterase inhibitor therapy in both conditions. In clinical practice, it is important that PDD should be recognised and appropriately treated. This review aims to outline the recently proposed clinical diagnostic criteria for PDD and to summarise the guidelines/recommendations published since 2006 on the use of cholinesterase inhibitors in the management of PDD. Although the cholinesterase inhibitor rivastigmine has recently been approved for the management of PDD, there remains a need for the development of novel therapies that can affect key mechanisms of the disease or prevent/delay patients with PD and mild cognitive impairment from progressing to PDD.</div>
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<s1>Parkinson's Disease and Movement Disorders Unit, Institut Clinic de Neurociencies, and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Hospital Clinic de Barcelona, Institut d'lnvestigacions Biomèdiques August Pi i Sunyer, Universitat de Barcelona</s1>
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<s1>INSERM.UPMC UMRS 610, Federation of Neurology, Salpêtrière Hospital; University of Paris</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>8 aut.</sZ>
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<s0>Parkinson's disease (PD) has long been considered predominantly a motor disorder. However, its frequent association with dementia, which contributes significantly to the morbidity and mortality of the condition, is gaining increasing recognition. PD dementia (PDD) has a unique clinical profile and neuropathology, distinct from Alzheimer's disease (AD). Cholinergic deficits, a feature of both AD and PDD, underlie the rationale for cholinesterase inhibitor therapy in both conditions. In clinical practice, it is important that PDD should be recognised and appropriately treated. This review aims to outline the recently proposed clinical diagnostic criteria for PDD and to summarise the guidelines/recommendations published since 2006 on the use of cholinesterase inhibitors in the management of PDD. Although the cholinesterase inhibitor rivastigmine has recently been approved for the management of PDD, there remains a need for the development of novel therapies that can affect key mechanisms of the disease or prevent/delay patients with PD and mild cognitive impairment from progressing to PDD.</s0>
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<s5>04</s5>
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<s5>37</s5>
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<s0>Syndrome extrapyramidal</s0>
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<s5>38</s5>
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<s0>Extrapiramidal síndrome</s0>
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<s0>Enfermedad degenerativa</s0>
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<s0>Pathologie du système nerveux central</s0>
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<s0>Central nervous system disease</s0>
<s5>40</s5>
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<s0>Sistema nervosio central patología</s0>
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<s0>Nervous system diseases</s0>
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<s0>Sistema nervioso patología</s0>
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<ET>Diagnosis and management of Parkinson's disease dementia</ET>
<AU>POEWE (W.); GAUTHIER (S.); AARSLAND (D.); LEVERENZ (J. B.); BARONE (P.); WEINTRAUB (D.); TOLOSA (E.); DUBOIS (B.)</AU>
<AF>Department of Neurology, Medical University Innsbruck/Innsbruck/Autriche (1 aut.); Alzheimer's Disease Research Unit, McGill Centre for Studies in Aging, Douglas Mental Health University Institute/Montréal, QC/Canada (2 aut.); Norweigen Centre for Movement Disorders, Stavenger University Hospital/Stavenger/Norvège (3 aut.); Institute of Clinical Medicine, University of Bergen/Bergen/Norvège (3 aut.); Mental Illness and Parkinson's Disease Research Education and Clinical Centers, VA-PSHCS, and Departments of Neurology and Psychiatry and Behavioral Sciences, University of Washington/Seattle, WA/Etats-Unis (4 aut.); Dipartimento di Scienze Neurologiche, Università Federico II di Napoli/Naples/Italie (5 aut.); Department of Psychiatry, University of Pennsylvania/Philadelphia, PA/Etats-Unis (6 aut.); Parkinson's Disease and Movement Disorders Unit, Institut Clinic de Neurociencies, and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Hospital Clinic de Barcelona, Institut d'lnvestigacions Biomèdiques August Pi i Sunyer, Universitat de Barcelona/Barcelona/Espagne (7 aut.); INSERM.UPMC UMRS 610, Federation of Neurology, Salpêtrière Hospital; University of Paris/Paris/France (8 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>International journal of clinical practice : (Esher); ISSN 1368-5031; Royaume-Uni; Da. 2008; Vol. 62; No. 10; Pp. 1581-1587; Bibl. 47 ref.</SO>
<LA>Anglais</LA>
<EA>Parkinson's disease (PD) has long been considered predominantly a motor disorder. However, its frequent association with dementia, which contributes significantly to the morbidity and mortality of the condition, is gaining increasing recognition. PD dementia (PDD) has a unique clinical profile and neuropathology, distinct from Alzheimer's disease (AD). Cholinergic deficits, a feature of both AD and PDD, underlie the rationale for cholinesterase inhibitor therapy in both conditions. In clinical practice, it is important that PDD should be recognised and appropriately treated. This review aims to outline the recently proposed clinical diagnostic criteria for PDD and to summarise the guidelines/recommendations published since 2006 on the use of cholinesterase inhibitors in the management of PDD. Although the cholinesterase inhibitor rivastigmine has recently been approved for the management of PDD, there remains a need for the development of novel therapies that can affect key mechanisms of the disease or prevent/delay patients with PD and mild cognitive impairment from progressing to PDD.</EA>
<CC>002B01; 002B17G</CC>
<FD>Maladie de Parkinson; Diagnostic; Conduite à tenir; Démence; Médecine</FD>
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<ED>Parkinson disease; Diagnosis; Clinical management; Dementia; Medicine</ED>
<EG>Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease; Nervous system diseases</EG>
<SD>Parkinson enfermedad; Diagnóstico; Actitud médica; Demencia; Medicina</SD>
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