Movement Disorders (revue)

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Effectiveness and Safety of Treatments for Degenerative Ataxias: A Systematic Review

Identifieur interne : 001E64 ( PascalFrancis/Curation ); précédent : 001E63; suivant : 001E65

Effectiveness and Safety of Treatments for Degenerative Ataxias: A Systematic Review

Auteurs : M. Mar Trujillo-Martin [Espagne] ; Pedro Serrano-Aguilar [Espagne] ; Fernando Monton-Alvarez [Espagne] ; Romen Carrillo-Fumero [Espagne]

Source :

RBID : Pascal:09-0301981

Descripteurs français

English descriptors

Abstract

The aim of this study was to determine the effectiveness and safety of available treatment alternatives for degenerative ataxias (DA). We systematically reviewed studies that assess pharmacological, rehabilitative, or psychological treatments in patients with DA. Studies were included if they fulfilled prespecified criteria. All included clinical trials were scored for methodological quality. Main outcome measures were clinical status of neurological disorder, adverse events, and patient-based factors. Twenty-five studies were included. Most studies were of small sample sizes, wide age variations, and low scientific validity. Only one study gave information on physical rehabilitation and none on psychological therapy. The remaining 24 studies reported on the effects of different pharmacological treatments. Outcomes such as functional capacity and psychological functioning of patients were evaluated by few studies. Some evidence supports that 5-hydroxy-tryptophan is more effective than placebo improving neurological symptoms in patients with Friedreich ataxia (FA), olivopontocerebellar atrophy, or cerebellar atrophy. Idebenone is more effective than placebo for halting and reversing the hypertrophic cardiomyopathy associated with FA, but it seems unable to improve neurological semiology. Limited evidence for other therapies was found. No relevant side effects for drugs that shown some degree of effectiveness were reported. Availability of quality studies to evaluate the safety and efficacy of treatments for most DA is scarce. No valid information on the actual value of physical rehabilitation and psychological support as treatments for DA is available. Further investigations with improved trial designs are necessary. © 2009 Movement Disorder Society.
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A11 02  1    @1 SERRANO-AGUILAR (Pedro)
A11 03  1    @1 MONTON-ALVAREZ (Fernando)
A11 04  1    @1 CARRILLO-FUMERO (Romen)
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A14 03      @1 CIBER Epidemiología y Salud Pública (CIBERESP) @3 ESP @Z 2 aut.
A14 04      @1 Department of Neurology, University Hospital of NaSade la Candelaria, Santa Cruz de Tenerife @2 Canary Islands @3 ESP @Z 3 aut.
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C01 01    ENG  @0 The aim of this study was to determine the effectiveness and safety of available treatment alternatives for degenerative ataxias (DA). We systematically reviewed studies that assess pharmacological, rehabilitative, or psychological treatments in patients with DA. Studies were included if they fulfilled prespecified criteria. All included clinical trials were scored for methodological quality. Main outcome measures were clinical status of neurological disorder, adverse events, and patient-based factors. Twenty-five studies were included. Most studies were of small sample sizes, wide age variations, and low scientific validity. Only one study gave information on physical rehabilitation and none on psychological therapy. The remaining 24 studies reported on the effects of different pharmacological treatments. Outcomes such as functional capacity and psychological functioning of patients were evaluated by few studies. Some evidence supports that 5-hydroxy-tryptophan is more effective than placebo improving neurological symptoms in patients with Friedreich ataxia (FA), olivopontocerebellar atrophy, or cerebellar atrophy. Idebenone is more effective than placebo for halting and reversing the hypertrophic cardiomyopathy associated with FA, but it seems unable to improve neurological semiology. Limited evidence for other therapies was found. No relevant side effects for drugs that shown some degree of effectiveness were reported. Availability of quality studies to evaluate the safety and efficacy of treatments for most DA is scarce. No valid information on the actual value of physical rehabilitation and psychological support as treatments for DA is available. Further investigations with improved trial designs are necessary. © 2009 Movement Disorder Society.
C02 01  X    @0 002B17
C02 02  X    @0 002B17G
C03 01  X  FRE  @0 Ataxie @5 01
C03 01  X  ENG  @0 Ataxia @5 01
C03 01  X  SPA  @0 Ataxia @5 01
C03 02  X  FRE  @0 Pathologie du système nerveux @5 02
C03 02  X  ENG  @0 Nervous system diseases @5 02
C03 02  X  SPA  @0 Sistema nervioso patología @5 02
C03 03  X  FRE  @0 Sécurité @5 09
C03 03  X  ENG  @0 Safety @5 09
C03 03  X  SPA  @0 Seguridad @5 09
C03 04  X  FRE  @0 Traitement @5 10
C03 04  X  ENG  @0 Treatment @5 10
C03 04  X  SPA  @0 Tratamiento @5 10
C03 05  X  FRE  @0 Maladie rare @4 CD @5 96
C03 05  X  ENG  @0 Rare disease @4 CD @5 96
C03 05  X  SPA  @0 Enfermedad rara @4 CD @5 96
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 Pathologie du système nerveux central @5 38
C07 02  X  ENG  @0 Central nervous system disease @5 38
C07 02  X  SPA  @0 Sistema nervosio central patología @5 38
C07 03  X  FRE  @0 Trouble neurologique @5 40
C07 03  X  ENG  @0 Neurological disorder @5 40
C07 03  X  SPA  @0 Trastorno neurológico @5 40
N21       @1 215
N44 01      @1 OTO
N82       @1 OTO

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Pascal:09-0301981

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