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

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The Movement Disorder Society Evidence-Based Medicine Review Update: Treatments for the Motor Symptoms of Parkinson's Disease

Identifieur interne : 000995 ( PascalFrancis/Curation ); précédent : 000994; suivant : 000996

The Movement Disorder Society Evidence-Based Medicine Review Update: Treatments for the Motor Symptoms of Parkinson's Disease

Auteurs : Susan H. Fox [Canada] ; Regina Katzenschlager [Autriche] ; Shen-Yang Lim [Malaisie] ; Bernard Ravina [États-Unis] ; Klaus Seppi [Autriche] ; Miguel Coelho [Portugal] ; Werner Poewe [Autriche] ; Olivier Rascol [France] ; Christopher G. Goetz [États-Unis] ; Cristina Sampaio [Portugal]

Source :

RBID : Pascal:11-0496525

Descripteurs français

English descriptors

Abstract

The objective was to update previous evidence-based medicine reviews of treatments for motor symptoms of Parkinson's disease published between 2002 and 2005. Level I (randomized, controlled trial) reports of pharmacological, surgical, and nonpharmacological interventions for the motor symptoms of Parkinson's disease between January 2004 (2001 for nonpharmacological) and December 2010 were reviewed. Criteria for inclusion, clinical indications, ranking, efficacy conclusions, safety, and implications for clinical practice followed the original program outline and adhered to evidence-based medicine methodology. Sixty-eight new studies qualified for review. Piribedil, pramipexole, pramipexole extended release, ropinirole, rotigotine, cabergoline, and pergolide were all efficacious as symptomatic monotherapy; ropinirole prolonged release was likely efficacious. All were efficacious as a symptomatic adjunct except pramipexole extended release, for which there is insufficient evidence. For prevention/delay of motor fluctuations, pramipexole and cabergoline were efficacious, and for prevention/delay of dyskinesia, pramipexole, ropinirole, ropinirole prolonged release, and cabergoline were all efficacious, whereas pergolide was likely efficacious. Duodenal infusion of levodopa was likely efficacious in the treatment of motor complications, but the practice implication is investigational. Entacapone was nonefficacious as a symptomatic adjunct to levodopa in nonfluctuating patients and nonefficacious in the prevention/delay of motor complications. Rasagiline conclusions were revised to efficacious as a symptomatic adjunct, and as treatment for motor fluctuations. Clozapine was efficacious in dyskinesia, but because of safety issues, the practice implication is possibly useful. Bilateral subthalamic nucleus deep brain stimulation, bilateral globus pallidus stimulation, and unilateral pallidotomy were updated to efficacious for motor complications. Physical therapy was revised to likely efficacious as symptomatic adjunct therapy. This evidence-based medicine review updates the field and highlights gaps for research.
pA  
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A03   1    @0 Mov. disord.
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A08 01  1  ENG  @1 The Movement Disorder Society Evidence-Based Medicine Review Update: Treatments for the Motor Symptoms of Parkinson's Disease
A09 01  1  ENG  @1 Evidence Based Medicine
A11 01  1    @1 FOX (Susan H.)
A11 02  1    @1 KATZENSCHLAGER (Regina)
A11 03  1    @1 LIM (Shen-Yang)
A11 04  1    @1 RAVINA (Bernard)
A11 05  1    @1 SEPPI (Klaus)
A11 06  1    @1 COELHO (Miguel)
A11 07  1    @1 POEWE (Werner)
A11 08  1    @1 RASCOL (Olivier)
A11 09  1    @1 GOETZ (Christopher G.)
A11 10  1    @1 SAMPAIO (Cristina)
A12 01  1    @1 SAMPAIO (Cristina) @9 ed.
A12 02  1    @1 SEPPI (Klaus) @9 ed.
A12 03  1    @1 FOX (Susan H.) @9 ed.
A14 01      @1 Movement Disorder Clinic, Toronto Western Hospital @2 Toronto, Ontario @3 CAN @Z 1 aut.
A14 02      @1 Department of Neurology, Danube Hospital/SMZ-Ost @2 Vienna @3 AUT @Z 2 aut.
A14 03      @1 Faculty of Medicine, University of Malaya @2 Kuala Lumpur @3 MYS @Z 3 aut.
A14 04      @1 Department of Neurology, University of Rochester School of Medicine @2 Rochester, New York @3 USA @Z 4 aut.
A14 05      @1 Department of Neurology, University Hospital @2 Innsbruck @3 AUT @Z 5 aut. @Z 7 aut.
A14 06      @1 Neurological Clinic Research Unit, Institute of Molecular Medicine, Lisbon School of Medicine @2 Lisbon @3 PRT @Z 6 aut. @Z 10 aut.
A14 07      @1 Department of Clinical Pharmacology, Toulouse University Hospital @2 Toulouse @3 FRA @Z 8 aut.
A14 08      @1 Department of Neurological Sciences, Rush University Medical Center @2 Chicago, Illinois @3 USA @Z 9 aut.
A15 01      @1 Movement Disorder Clinic, Toronto Western Hospital @2 Toronto, Ontario @3 CAN @Z 3 aut.
A15 02      @1 Department of Neurology, University Hospital @2 Innsbruck @3 AUT @Z 2 aut.
A15 03      @1 Department of Neurological Sciences, Rush University Medical Center @2 Chicago, Illinois @3 USA @Z 1 aut.
A20       @2 S2-S41
A21       @1 2011
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000505556490010
A44       @0 0000 @1 © 2011 INIST-CNRS. All rights reserved.
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C01 01    ENG  @0 The objective was to update previous evidence-based medicine reviews of treatments for motor symptoms of Parkinson's disease published between 2002 and 2005. Level I (randomized, controlled trial) reports of pharmacological, surgical, and nonpharmacological interventions for the motor symptoms of Parkinson's disease between January 2004 (2001 for nonpharmacological) and December 2010 were reviewed. Criteria for inclusion, clinical indications, ranking, efficacy conclusions, safety, and implications for clinical practice followed the original program outline and adhered to evidence-based medicine methodology. Sixty-eight new studies qualified for review. Piribedil, pramipexole, pramipexole extended release, ropinirole, rotigotine, cabergoline, and pergolide were all efficacious as symptomatic monotherapy; ropinirole prolonged release was likely efficacious. All were efficacious as a symptomatic adjunct except pramipexole extended release, for which there is insufficient evidence. For prevention/delay of motor fluctuations, pramipexole and cabergoline were efficacious, and for prevention/delay of dyskinesia, pramipexole, ropinirole, ropinirole prolonged release, and cabergoline were all efficacious, whereas pergolide was likely efficacious. Duodenal infusion of levodopa was likely efficacious in the treatment of motor complications, but the practice implication is investigational. Entacapone was nonefficacious as a symptomatic adjunct to levodopa in nonfluctuating patients and nonefficacious in the prevention/delay of motor complications. Rasagiline conclusions were revised to efficacious as a symptomatic adjunct, and as treatment for motor fluctuations. Clozapine was efficacious in dyskinesia, but because of safety issues, the practice implication is possibly useful. Bilateral subthalamic nucleus deep brain stimulation, bilateral globus pallidus stimulation, and unilateral pallidotomy were updated to efficacious for motor complications. Physical therapy was revised to likely efficacious as symptomatic adjunct therapy. This evidence-based medicine review updates the field and highlights gaps for research.
C02 01  X    @0 002B17
C02 02  X    @0 002B17G
C03 01  X  FRE  @0 Trouble moteur @5 01
C03 01  X  ENG  @0 Motor system disorder @5 01
C03 01  X  SPA  @0 Trastorno motor @5 01
C03 02  X  FRE  @0 Maladie de Parkinson @2 NM @5 02
C03 02  X  ENG  @0 Parkinson disease @2 NM @5 02
C03 02  X  SPA  @0 Parkinson enfermedad @2 NM @5 02
C03 03  X  FRE  @0 Pathologie du système nerveux @5 03
C03 03  X  ENG  @0 Nervous system diseases @5 03
C03 03  X  SPA  @0 Sistema nervioso patología @5 03
C03 04  X  FRE  @0 Médecine factuelle @5 09
C03 04  X  ENG  @0 Evidence-based medicine @5 09
C03 04  X  SPA  @0 Medicina basada en pruebas @5 09
C03 05  X  FRE  @0 Traitement @5 10
C03 05  X  ENG  @0 Treatment @5 10
C03 05  X  SPA  @0 Tratamiento @5 10
C03 06  X  FRE  @0 Lévodopa @2 NK @2 FR @5 11
C03 06  X  ENG  @0 Levodopa @2 NK @2 FR @5 11
C03 06  X  SPA  @0 Levodopa @2 NK @2 FR @5 11
C03 07  X  FRE  @0 Stimulant dopaminergique @5 12
C03 07  X  ENG  @0 Dopamine agonist @5 12
C03 07  X  SPA  @0 Estimulante dopaminérgico @5 12
C03 08  X  FRE  @0 Amine oxidase (flavin-containing) @2 FE @5 13
C03 08  X  ENG  @0 Amine oxidase (flavin-containing) @2 FE @5 13
C03 08  X  SPA  @0 Amine oxidase (flavin-containing) @2 FE @5 13
C03 09  X  FRE  @0 Transferases @2 FE @5 14
C03 09  X  ENG  @0 Transferases @2 FE @5 14
C03 09  X  SPA  @0 Transferases @2 FE @5 14
C03 10  X  FRE  @0 Amantadine @2 NK @2 FR @5 15
C03 10  X  ENG  @0 Amantadine @2 NK @2 FR @5 15
C03 10  X  SPA  @0 Amantadina @2 NK @2 FR @5 15
C03 11  X  FRE  @0 Clozapine @2 NK @2 FR @5 16
C03 11  X  ENG  @0 Clozapine @2 NK @2 FR @5 16
C03 11  X  SPA  @0 Clozapina @2 NK @2 FR @5 16
C03 12  X  FRE  @0 Exercice physique @5 17
C03 12  X  ENG  @0 Physical exercise @5 17
C03 12  X  SPA  @0 Ejercicio físico @5 17
C03 13  X  FRE  @0 Parole @5 18
C03 13  X  ENG  @0 Speech @5 18
C03 13  X  SPA  @0 Habla @5 18
C03 14  X  FRE  @0 Acupuncture @5 19
C03 14  X  ENG  @0 Acupuncture @5 19
C03 14  X  SPA  @0 Acupuntura @5 19
C03 15  X  FRE  @0 Stimulation cérébrale profonde @4 CD @5 96
C03 15  X  ENG  @0 Deep brain stimulation @4 CD @5 96
C07 01  X  FRE  @0 Pratique basée sur des preuves
C07 01  X  ENG  @0 Evidence-based practice
C07 01  X  SPA  @0 Práctica basada en la evidencia
C07 02  X  FRE  @0 Oxidoreductases @2 FE
C07 02  X  ENG  @0 Oxidoreductases @2 FE
C07 02  X  SPA  @0 Oxidoreductases @2 FE
C07 03  X  FRE  @0 Enzyme @2 FE
C07 03  X  ENG  @0 Enzyme @2 FE
C07 03  X  SPA  @0 Enzima @2 FE
C07 04  X  FRE  @0 Trouble neurologique @5 38
C07 04  X  ENG  @0 Neurological disorder @5 38
C07 04  X  SPA  @0 Trastorno neurológico @5 38
C07 05  X  FRE  @0 Pathologie de l'encéphale @5 39
C07 05  X  ENG  @0 Cerebral disorder @5 39
C07 05  X  SPA  @0 Encéfalo patología @5 39
C07 06  X  FRE  @0 Syndrome extrapyramidal @5 40
C07 06  X  ENG  @0 Extrapyramidal syndrome @5 40
C07 06  X  SPA  @0 Extrapiramidal síndrome @5 40
C07 07  X  FRE  @0 Maladie dégénérative @5 41
C07 07  X  ENG  @0 Degenerative disease @5 41
C07 07  X  SPA  @0 Enfermedad degenerativa @5 41
C07 08  X  FRE  @0 Pathologie du système nerveux central @5 42
C07 08  X  ENG  @0 Central nervous system disease @5 42
C07 08  X  SPA  @0 Sistema nervosio central patología @5 42
N21       @1 346
N44 01      @1 OTO
N82       @1 OTO

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Pascal:11-0496525

Le document en format XML

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<div type="abstract" xml:lang="en">The objective was to update previous evidence-based medicine reviews of treatments for motor symptoms of Parkinson's disease published between 2002 and 2005. Level I (randomized, controlled trial) reports of pharmacological, surgical, and nonpharmacological interventions for the motor symptoms of Parkinson's disease between January 2004 (2001 for nonpharmacological) and December 2010 were reviewed. Criteria for inclusion, clinical indications, ranking, efficacy conclusions, safety, and implications for clinical practice followed the original program outline and adhered to evidence-based medicine methodology. Sixty-eight new studies qualified for review. Piribedil, pramipexole, pramipexole extended release, ropinirole, rotigotine, cabergoline, and pergolide were all efficacious as symptomatic monotherapy; ropinirole prolonged release was likely efficacious. All were efficacious as a symptomatic adjunct except pramipexole extended release, for which there is insufficient evidence. For prevention/delay of motor fluctuations, pramipexole and cabergoline were efficacious, and for prevention/delay of dyskinesia, pramipexole, ropinirole, ropinirole prolonged release, and cabergoline were all efficacious, whereas pergolide was likely efficacious. Duodenal infusion of levodopa was likely efficacious in the treatment of motor complications, but the practice implication is investigational. Entacapone was nonefficacious as a symptomatic adjunct to levodopa in nonfluctuating patients and nonefficacious in the prevention/delay of motor complications. Rasagiline conclusions were revised to efficacious as a symptomatic adjunct, and as treatment for motor fluctuations. Clozapine was efficacious in dyskinesia, but because of safety issues, the practice implication is possibly useful. Bilateral subthalamic nucleus deep brain stimulation, bilateral globus pallidus stimulation, and unilateral pallidotomy were updated to efficacious for motor complications. Physical therapy was revised to likely efficacious as symptomatic adjunct therapy. This evidence-based medicine review updates the field and highlights gaps for research.</div>
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