TY - JOUR
T1 - Comparing the Value of Data Visualization Methods for Communicating Harms in Clinical Trials
AU - Qureshi, Riaz
AU - Chen, Xiwei
AU - Goerg, Carsten
AU - Mayo-Wilson, Evan
AU - Dickinson, Stephanie
AU - Golzarri-Arroyo, Lilian
AU - Hong, Hwanhee
AU - Phillips, Rachel
AU - Cornelius, Victoria
AU - DeMarco, Mara Mc Adams
AU - Guallar, Eliseo
AU - Li, Tianjing
N1 - Publisher Copyright:
© The Author(s) 2022. Published by Oxford University Press on behalf of the Johns Hopkins Bloomberg School of Public Health.
PY - 2022
Y1 - 2022
N2 - In clinical trials, harms (i.e., adverse events) are often reported by simply counting the number of people who experienced each event. Reporting only frequencies ignores other dimensions of the data that are important for stakeholders, including severity, seriousness, rate (recurrence), timing, and groups of related harms. Additionally, application of selection criteria to harms prevents most from being reported. Visualization of data could improve communication of multidimensional data. We replicated and compared the characteristics of 6 different approaches for visualizing harms: dot plot, stacked bar chart, volcano plot, heat map, treemap, and tendril plot. We considered binary events using individual participant data from a randomized trial of gabapentin for neuropathic pain. We assessed their value using a heuristic approach and a group of content experts. We produced all figures using R and share the open-source code on GitHub. Most original visualizations propose presenting individual harms (e.g., dizziness, somnolence) alone or alongside higher level (e.g., by body systems) summaries of harms, although they could be applied at either level. Visualizations can present different dimensions of all harms observed in trials. Except for the tendril plot, all other plots do not require individual participant data. The dot plot and volcano plot are favored as visualization approaches to present an overall summary of harms data. Our value assessment found the dot plot and volcano plot were favored by content experts. Using visualizations to report harms could improve communication. Trialists can use our provided code to easily implement these approaches.
AB - In clinical trials, harms (i.e., adverse events) are often reported by simply counting the number of people who experienced each event. Reporting only frequencies ignores other dimensions of the data that are important for stakeholders, including severity, seriousness, rate (recurrence), timing, and groups of related harms. Additionally, application of selection criteria to harms prevents most from being reported. Visualization of data could improve communication of multidimensional data. We replicated and compared the characteristics of 6 different approaches for visualizing harms: dot plot, stacked bar chart, volcano plot, heat map, treemap, and tendril plot. We considered binary events using individual participant data from a randomized trial of gabapentin for neuropathic pain. We assessed their value using a heuristic approach and a group of content experts. We produced all figures using R and share the open-source code on GitHub. Most original visualizations propose presenting individual harms (e.g., dizziness, somnolence) alone or alongside higher level (e.g., by body systems) summaries of harms, although they could be applied at either level. Visualizations can present different dimensions of all harms observed in trials. Except for the tendril plot, all other plots do not require individual participant data. The dot plot and volcano plot are favored as visualization approaches to present an overall summary of harms data. Our value assessment found the dot plot and volcano plot were favored by content experts. Using visualizations to report harms could improve communication. Trialists can use our provided code to easily implement these approaches.
KW - adverse events
KW - controlled clinical trials
KW - data visualization
KW - drug-related side effects and adverse reactions
KW - harms
KW - health communication
KW - randomized controlled trials
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U2 - 10.1093/epirev/mxac005
DO - 10.1093/epirev/mxac005
M3 - Review article
C2 - 36065832
AN - SCOPUS:85144596684
SN - 0193-936X
VL - 44
SP - 55
EP - 66
JO - Epidemiologic Reviews
JF - Epidemiologic Reviews
IS - 1
ER -