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Cochrane Database of Systematic Reviews

Pharmacological and nutritional treatment for McArdle disease (Glycogen Storage Disease type V)

Esta versión no es la más reciente

Información

DOI:
https://doi.org/10.1002/14651858.CD003458.pub4Copiar DOI
Base de datos:
  1. Cochrane Database of Systematic Reviews
Versión publicada:
  1. 08 diciembre 2010see what's new
Tipo:
  1. Intervention
Etapa:
  1. Review
Grupo Editorial Cochrane:
  1. Grupo Cochrane de Neuromuscular

Copyright:
  1. Copyright © 2010 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

Cifras del artículo

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Autores

  • Rosaline Quinlivan

    Correspondencia a: MRC Centre for Neuromuscular Diseases and Dubowitz Neuromuscular Centre, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery and Great Ormond Street, London, UK

    [email protected]

  • Andrea Martinuzzi

    The Conegliano‐Pieve Research Centre, Medea Scientific Institute, Conegliano, Italy

  • Benedikt Schoser

    Department of Neurology, Friedrich‐Baur Institute Ludwig‐Maximilians University Munich, D‐80336 Munich, Germany

Contributions of authors

RQ and RB were involved in the original review and agreed criteria for inclusion of studies and their methodological quality. RQ and MA were involved in assessing the two new studies included in the updated review. RQ completed the first and second updated drafts with agreement and approval from RB and MA. RQ completed this update with agreement and approval of AM and BS.

Sources of support

Internal sources

  • None, Not specified.

External sources

  • None, Not specified.

Declarations of interest

Two authors (RB and RQ) were involved in the conduct of a randomized cross‐over placebo controlled trial of vitamin B6, which did not demonstrate any overall benefit. One author (AM) was involved in the conduct of a randomized controlled trial of ramipril which did not demonstrate any significant benefit. One author (BS) was involved in an unblinded observational study of high fat diet which showed no benefit.

Acknowledgements

Rob Beynon was second author in the original review and first two updates.

We thank the Muscular Dystrophy Campaign of Great Britain and the Association for Glycogen Storage Diseases (AGSD). We dedicate this review to Nicholas Owston, who sadly died in 2003, in acknowledgement of his untiring support through the AGSD.

Editorial support from the Cochrane Neuromuscular Disease Group was funded by the TREAT NMD Network European Union Grant 036825.

Version history

Published

Title

Stage

Authors

Version

2014 Nov 12

Pharmacological and nutritional treatment for McArdle disease (Glycogen Storage Disease type V)

Review

Rosaline Quinlivan, Andrea Martinuzzi, Benedikt Schoser

https://doi.org/10.1002/14651858.CD003458.pub5

2010 Dec 08

Pharmacological and nutritional treatment for McArdle disease (Glycogen Storage Disease type V)

Review

Rosaline Quinlivan, Andrea Martinuzzi, Benedikt Schoser

https://doi.org/10.1002/14651858.CD003458.pub4

2008 Apr 23

Pharmacological and nutritional treatment for McArdle disease (Glycogen Storage Disease type V)

Review

Rosaline Quinlivan, Robert J Beynon, Andrea Martinuzzi

https://doi.org/10.1002/14651858.CD003458.pub3

2004 Jul 19

Pharmacological and nutritional treatment for McArdle's disease (Glycogen Storage Disease type V)

Review

Rosaline Quinlivan, Robert J Beynon

https://doi.org/10.1002/14651858.CD003458.pub2

2002 Jan 21

Pharmacological and nutritional treatment for McArdle's disease (Glycogen storage disease type V)

Protocol

Ros Quinlivan, Robert J Beynon

https://doi.org/10.1002/14651858.CD003458

Differences between protocol and review

In this update of the review, the most recent trials were assessed for risk of bias according to the new Cochrane risk of bias assessment method (Higgins 2008).

PICO

Population
Intervention
Comparison
Outcome

El uso y la enseñanza del modelo PICO están muy extendidos en el ámbito de la atención sanitaria basada en la evidencia para formular preguntas y estrategias de búsqueda y para caracterizar estudios o metanálisis clínicos. PICO son las siglas en inglés de cuatro posibles componentes de una pregunta de investigación: paciente, población o problema; intervención; comparación; desenlace (outcome).

Para saber más sobre el uso del modelo PICO, puede consultar el Manual Cochrane.