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...

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Detalhes bibliográficos
Publicado no:Eur J Cancer Care (Engl)
Main Authors: Sztankay, Monika, Neppl, Lucia, Wintner, Lisa M., Loth, Fanny L., Willenbacher, Wolfgang, Weger, Roman, Weyrer, Walpurga, Steurer, Michael, Rumpold, Gerhard, Holzner, Bernhard
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2019
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6900154/
https://ncbi.nlm.nih.gov/pubmed/31465136
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ecc.13154
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