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

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

Publikováno v: Nephrology, dialysis, transplantation, 30(10), 1605-1614. Oxford University Press
Nephrology Dialysis Transplantation
Nephrology Dialysis Transplantation, Oxford University Press (OUP), 2015, 30 (10), pp.1605-1614. ⟨10.1093/ndt/gfv209⟩
Nephrology Dialysis Transplantation, Oxford University Press (OUP), 2015, 30 (10), pp.1605-1614. 〈10.1093/ndt/gfv209〉

International audience; 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 regis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ada3e9d863c69d757a83ae84b1491489
https://pure.amc.nl/en/publications/how-to-routinely-collect-data-on-patientreported-outcome-and-experience-measures-in-renal-registries-in-europe-an-expert-consensus-meeting(1457fdaa-941d-47fc-a6ca-6627a7e5e89c).html