How to routinely collect data on patient-reported outcome and experience measures in renal registries in Europe: an expert consensus meeting-Reference-Cited by-同舟云学术

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

Published:2015-05-16 Issue:10 Volume:30 Page:1605-1614
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:Nephrol. Dial. Transplant.

Author:

Breckenridge Kate,Bekker Hillary L.,Gibbons Elizabeth,van der Veer Sabine N.,Abbott Denise,Briançon Serge,Cullen Ron,Garneata Liliana,Jager Kitty J.,Lønning Kjersti,Metcalfe Wendy,Morton Rachael L.,Murtagh Fliss E.M.,Prutz Karl,Robertson Susan,Rychlik Ivan,Schon Steffan,Sharp Linda,Speyer Elodie,Tentori Francesca,Caskey Fergus J.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/30/10/1605/17172533/gfv209.pdf

Reference83 articles.

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4. The applications of PROs in clinical practice: what are they, do they work, and why?

5. Capture, Transfer, and Feedback of Patient-Centered Outcomes Data in Palliative Care Populations: Does It Make a Difference? A Systematic Review

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