How to routinely collect data on patient-reported outcome and experience measures in renal registries in Europe: an expert consensus meeting

Breckenridge, K, Bekker, HL, Gibbons, E et al. (18 more authors) (2015) How to routinely collect data on patient-reported outcome and experience measures in renal registries in Europe: an expert consensus meeting. Nephrology Dialysis Transplantation, 30 (10). pp. 1605-1614. ISSN 0931-0509

Abstract

Metadata

Authors/Creators:
  • Breckenridge, K
  • Bekker, HL
  • Gibbons, E
  • van der Veer, SN
  • Abbott, D
  • Briancon, S
  • Cullen, R
  • Garneata, L
  • Jager, KJ
  • Lonning, K
  • Metcalfe, W
  • Morton, RL
  • Murtagh, FEM
  • Prutz, K
  • Robertson, S
  • Rychlik, I
  • Schon, S
  • Sharp, L
  • Speyer, E
  • Tentori, F
  • Caskey, FJ
Copyright, Publisher and Additional Information: © The Author 2015. Published by Oxford University Press on behalf of ERA-EDTA. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: patient-reported measures; quality indicators; registry
Dates:
  • Published: October 2015
  • Accepted: 13 April 2015
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Medicine (Leeds) > Leeds Institute of Health Sciences (Leeds) > Academic Unit of Psychiatry and Behavioural Sciences (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 11 Jan 2016 16:19
Last Modified: 12 Feb 2019 13:04
Published Version: http://dx.doi.org/10.1093/ndt/gfv209
Status: Published
Publisher: Oxford University Press
Identification Number: https://doi.org/10.1093/ndt/gfv209
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