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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)
- Source :
- Journal of the American Medical Informatics Association. 26:276-285
- Publication Year :
- 2019
- Publisher :
- Oxford University Press (OUP), 2019.
-
Abstract
- 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 Methods Patients in 3 multicenter trials electronically completed surveys during cancer treatment. Each survey included a prespecified subset of items from the National Cancer Institute’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE). Upon completion of the survey items, patients could add supplemental symptomatic AE information in a free text box. As patients typed into the box, structured dropdown terms could be selected from the PRO-CTCAE item library or Medical Dictionary for Regulatory Activities (MedDRA), or patients could type unstructured free text for submission. Results Data were pooled from 1760 participants (48% women; 78% White) who completed 8892 surveys, of which 2387 (26.8%) included supplemental symptomatic AE information. Overall, 1024 (58%) patients entered supplemental information at least once, with an average of 2.3 per patient per study. This encompassed 1474 of 8892 (16.6%) dropdowns and 913 of 8892 (10.3%) unstructured free text entries. One-third of the unstructured free text entries (32%) could be mapped post hoc to a PRO-CTCAE term and 68% to a MedDRA term. Discussion Participants frequently added supplemental information beyond study-specific survey items. Almost half selected a structured dropdown term, although many opted to submit unstructured free text entries. Most free text entries could be mapped post hoc to PRO-CTCAE or MedDRA terms, suggesting opportunities to enhance the system to perform real-time mapping for AE reporting. Conclusions Patient reporting of symptomatic AEs using a text box functionality with mapping to existing terminologies is both feasible and informative.
- Subjects :
- Adult
Male
medicine.medical_specialty
Drug-Related Side Effects and Adverse Reactions
MedDRA
Antineoplastic Agents
Health Informatics
Research and Applications
Pro ctcae
User-Computer Interface
03 medical and health sciences
0302 clinical medicine
Neoplasms
Text messaging
Adverse Drug Reaction Reporting Systems
Humans
Medicine
Patient Reported Outcome Measures
030212 general & internal medicine
Adverse effect
Aged
Aged, 80 and over
Internet
business.industry
Cancer
Common Terminology Criteria for Adverse Events
Middle Aged
medicine.disease
National Cancer Institute (U.S.)
United States
Text box
Clinical research
030220 oncology & carcinogenesis
Family medicine
Drug Evaluation
Female
Self Report
business
Software
Subjects
Details
- ISSN :
- 1527974X
- Volume :
- 26
- Database :
- OpenAIRE
- Journal :
- Journal of the American Medical Informatics Association
- Accession number :
- edsair.doi.dedup.....e972117768beda4590d5cf05bf34a445
- Full Text :
- https://doi.org/10.1093/jamia/ocy169