The importance of data issues when comparing cystic fibrosis registry outcomes between countries: Are annual review FEV1 in the UK only collected when subjects are well?

Hoo, Z. orcid.org/0000-0002-7067-3783, Curley, R., Campbell, M.J. et al. (2 more authors) (2018) The importance of data issues when comparing cystic fibrosis registry outcomes between countries: Are annual review FEV1 in the UK only collected when subjects are well? Journal of Evaluation in Clinical Practice. ISSN 1356-1294

Abstract

Metadata

Authors/Creators:
Copyright, Publisher and Additional Information: © 2018 The Authors Journal of Evaluation in Clinical Practice Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. (http://creativecommons.org/licenses/by/4.0/)
Keywords: clinical epidemiology; cystic fibrosis; respiratory measurement
Dates:
  • Accepted: 22 May 2018
  • Published (online): 14 June 2018
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > School of Health and Related Research (Sheffield) > Sheffield Centre for Health and Related Research
The University of Sheffield > Sheffield Teaching Hospitals
Funding Information:
FunderGrant number
NATIONAL INSTITUTE FOR HEALTH RESEARCHDRF-2014-07-092
Depositing User: Symplectic Sheffield
Date Deposited: 19 Jun 2018 14:56
Last Modified: 19 Jun 2018 14:56
Published Version: https://doi.org/10.1111/jep.12967
Status: Published online
Publisher: Wiley
Refereed: Yes
Identification Number: https://doi.org/10.1111/jep.12967

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