Complementing clinical cancer registry data with patient reported outcomes: A feasibility study on routine electronic patient‐reported outcome assessment for the Austrian Myelome Registry

OBJECTIVES: Routinely assessed patient‐reported outcomes (PROs), such as quality of life (QOL), are important to supplement clinical cancer data but requires rigorous implementation. This study aims at depicting the implementation procedure and evaluating the feasibility of routine electronic PRO mo...

Descripción completa

Detalles Bibliográficos
Autores principales: Sztankay, Monika, Neppl, Lucia, Wintner, Lisa M., Loth, Fanny L., Willenbacher, Wolfgang, Weger, Roman, Weyrer, Walpurga, Steurer, Michael, Rumpold, Gerhard, Holzner, Bernhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6900154/
https://www.ncbi.nlm.nih.gov/pubmed/31465136
http://dx.doi.org/10.1111/ecc.13154

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6900154/
https://www.ncbi.nlm.nih.gov/pubmed/31465136
http://dx.doi.org/10.1111/ecc.13154

Ejemplares similares