Reliability and validity of PRO-CTCAE® daily reporting with a 24-hour recall period

PURPOSE: The standard recall period for the patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE®) is the past 7 days, but there are contexts where a 24-hour recall may be desirable. The purpose of this analysis was to investigate the reliability and val...

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Detalles Bibliográficos
Autores principales: Lee, M. K., Basch, E., Mitchell, S. A., Minasian, L. M., Langlais, B. T., Thanarajasingam, G., Ginos, B. F., Rogak, L. J., Mendoza, T. R., Bennett, A. V., Schrag, D., Mazza, G. L., Dueck, A. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241696/
https://www.ncbi.nlm.nih.gov/pubmed/36897529
http://dx.doi.org/10.1007/s11136-023-03374-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241696/
https://www.ncbi.nlm.nih.gov/pubmed/36897529
http://dx.doi.org/10.1007/s11136-023-03374-5

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