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Cochrane Database of Systematic Reviews

Enteral tube feeding for cystic fibrosis

Información

DOI:
https://doi.org/10.1002/14651858.CD001198.pub5Copiar DOI
Base de datos:
  1. Cochrane Database of Systematic Reviews
Versión publicada:
  1. 22 julio 2019see what's new
Tipo:
  1. Intervention
Etapa:
  1. Review
Grupo Editorial Cochrane:
  1. Grupo Cochrane de Fibrosis quística y enfermedades genéticas

Copyright:
  1. Copyright © 2019 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

Cifras del artículo

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Autores

  • Deirdre Shimmin

    Correspondencia a: Adult Cystic Fibrosis Unit, St James's University Hospital , Leeds, UK

    [email protected]

  • Jacqueline Lowdon

    Leeds Regional Paediatric Cystic Fibrosis Centre, Leeds Teaching Hospitals NHS Trust, Leeds, UK

  • Tracey Remmington

    Department of Women's and Children's Health, University of Liverpool, Liverpool, UK

Contributions of authors

Each author independently evaluated each paper and contributed equally to the final review paper.

Sources of support

Internal sources

  • No sources of support supplied

External sources

  • National Institute for Health Research, UK

    This systematic review was supported by the National Institute for Health Research, via Cochrane Infrastructure funding to the Cochrane Cystic Fibrosis and Genetic Disorders Group.

Declarations of interest

Dee Shimmin has no declarations of interest to make.

Jacqueline Lowdon has received payment from Nutricia as co‐editor of a quarterly paediatric newsletter and sponsorship from Gilead to attend a CF conference.

Tracey Remmingtion has no declarations of interest to make.

Acknowledgements

We would like to acknowledge the previous input of the former authors on this review, Dr Steve Conway, Alison Morton and Sue Wolfe.

This project was supported by the National Institute for Health Research, via Cochrane Infrastructure funding to the Cochrane Cystic Fibrosis and Genetic Disorders Group. The views and opinions expressed therein are those of the authors and do not necessarily reflect those of the Systematic Reviews Programme, NIHR, NHS or the Department of Health.

Version history

Published

Title

Stage

Authors

Version

2019 Jul 22

Enteral tube feeding for cystic fibrosis

Review

Deirdre Shimmin, Jacqueline Lowdon, Tracey Remmington

https://doi.org/10.1002/14651858.CD001198.pub5

2015 Apr 09

Enteral tube feeding for cystic fibrosis

Review

Alison Morton, Susan Wolfe

https://doi.org/10.1002/14651858.CD001198.pub4

2012 Dec 12

Enteral tube feeding for cystic fibrosis

Review

Steven Conway, Alison Morton, Susan Wolfe

https://doi.org/10.1002/14651858.CD001198.pub3

2008 Apr 23

Enteral tube feeding for cystic fibrosis

Review

Steven Conway, Alison Morton, Susan Wolfe

https://doi.org/10.1002/14651858.CD001198.pub2

1999 Jul 26

Enteral tube feeding for cystic fibrosis

Review

Steven Conway, Alison Morton, Susan Wolfe

https://doi.org/10.1002/14651858.CD001198

Differences between protocol and review

At the update in 2012, we added the outcome BMI percentile position as we feel this is a clinically relevant outcome.

Keywords

MeSH

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.