Patient free text reporting of symptomatic adverse events in cancer clinical research using the National Cancer Institute’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)

OBJECTIVE: The study sought to describe patient-entered supplemental information on symptomatic adverse events (AEs) in cancer clinical research reported via a National Cancer Institute software system and examine the feasibility of mapping these entries to established terminologies. MATERIALS AND M...

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Detalles Bibliográficos
Publicado en:J Am Med Inform Assoc
Main Authors: Chung, Arlene E, Shoenbill, Kimberly, Mitchell, Sandra A, Dueck, Amylou C, Schrag, Deborah, Bruner, Deborah W, Minasian, Lori M, St. Germain, Diane, O’Mara, Ann M, Baumgartner, Paul, Rogak, Lauren J, Abernethy, Amy P, Griffin, Ashley C, Basch, Ethan M
Formato: Artigo
Idioma:Inglês
Publicado: Oxford University Press 2019
Assuntos:
Research and Applications
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6402312/
https://ncbi.nlm.nih.gov/pubmed/30840079
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jamia/ocy169
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