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Published on: August 9, 2024
The Impact of Web-Based Continuing Medical Education Using Patient Simulation on Real-World Treatment Selection in
Katie Stringer Lucero1, Amy Larkin1, Stanislav Zakharkin1
1Medscape, LLC, New York, NY, United States.
A web-based continuing medical education (CME) simulation improved real-world prescribing of glucagon-like peptide-1 receptor agonists (GLP-1 RAs) for type 2 diabetes patients. This intervention increased the use of evidence-based treatments for cardiovascular risk reduction.
Area of Science:
- Endocrinology
- Medical Education
- Cardiovascular Disease Prevention
Background:
- Guidelines recommend glucagon-like peptide-1 receptor agonists (GLP-1 RAs) for type 2 diabetes (T2D), but uptake is suboptimal.
- Web-based continuing medical education (CME) patient simulations can identify practice gaps but their real-world impact is unstudied.
Purpose of the Study:
- To evaluate the impact of a simulation-based CME intervention on the real-world prescription patterns of GLP-1 RAs.
- To assess if CME simulations improve the selection of evidence-based treatments for T2D patients, focusing on glycemic control and cardiovascular protection.
Main Methods:
- A two-phase study involving 435 physicians in the US.
- Phase I: Paired pre-post CME simulation to assess decision-making improvements.
- Phase II: Retrospective, matched case-control study of 157 physicians using claims data to evaluate real-world treatment changes.
Main Results:
- CME simulation significantly improved correct treatment decisions by 29 percentage points (40.9% to 69.9%, P<.001).
- Physicians in the intervention group were more likely to increase GLP-1 RA use (24.8% vs 12.7%, P=.001).
- Intervention group participation predicted increased GLP-1 RA use (OR 4.49, 95% CI 1.45-13.97).
Conclusions:
- A web-based CME simulation targeting secondary cardiovascular prevention in T2D is associated with improved real-world, evidence-based treatment selection.
- Simulation-based CME can be an effective tool to bridge the gap between guideline recommendations and clinical practice for GLP-1 RA utilization.
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