ArticleFrontiers in medicine2025
Utilizing group-based models to identify adverse event patterns after an intervention.
Article in Frontiers in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
6 authors.
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Abstract
Background: Standard adverse event (AE) monitoring only records whether events occur after the intervention, and not whether these events vary over time. Objective: To test whether there were statistically distinct time-varying trajectories of AE (e.g., "side effects") after an intervention and identify characteristics of individuals associated with these patterns. Design: Group-based trajectory models applied to an observational study of individuals who received one or two doses of a mRNA COVID-19 vaccine (i.e., the intervention). Participants: 50,484 healthcare personnel who received their vaccinations within the Mass General Brigham (MGB) healthcare system. Interventions: Vaccination. Main measures: Allergic and non-allergic AE for 1-3 days after each of two COVID-19 vaccinations. Key results: Trajectories models identified distinct groups with different trajectories after intervention: two groups after the first vaccination and five groups after the second vaccination. These groups differed by demographics, age, prior prescription for epinephrine auto-injectors, prior COVID-19 history, time-of-day of vaccination, and vaccine manufacturer. Conclusion: Several different time-based trajectories after the intervention (e.g., first two COVID-19 vaccinations) were noted; individuals in these groups varied by demographic and clinical criteria. These time-based methods may be able to identify groups at higher risk of future adverse reactions, provide a basis for future studies of the physiology underlying these risk differentials, and improve counseling surrounding interventions associated with AEs. We suggest that trajectory-based methods be added to post-intervention surveillance.
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