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

Despite the potential for patient-reported outcome measures (PROMs) and experience measures (PREMs) to enhance understanding of patient experiences and outcomes they have not, to date, been widely incorporated into renal registry datasets. This report summarizes the main points learned from an ERA-E...

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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Cutting-Edge Renal Science
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569391/
https://www.ncbi.nlm.nih.gov/pubmed/25982327
http://dx.doi.org/10.1093/ndt/gfv209

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569391/
https://www.ncbi.nlm.nih.gov/pubmed/25982327
http://dx.doi.org/10.1093/ndt/gfv209

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