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Updated: Apr 22, 2026

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Published on: March 15, 2022
Contemporary use of dual antiplatelet therapy for preventing cardiovascular events
Andrew M Goldsweig, Kimberly J Reid, Kensey Gosch
1Kaiser Permanente, Mid-Atlantic Permanente Research Institute, 2101 East Jefferson St, 3 West, Rockville, MD 20852.
Insights
Dual antiplatelet therapy (DAPT) use is low and decreasing in high-risk patients without established cardiovascular disease, following CHARISMA trial findings. DAPT use remains stable in patients with established cardiovascular disease.
Area of Science:
- Cardiology
- Clinical Trials
- Pharmacology
Background:
- The CHARISMA trial did not show dual antiplatelet therapy (DAPT) benefits over aspirin alone for cardiovascular events.
- Subgroup analyses suggested DAPT may reduce events in established cardiovascular disease (CVD) but increase events in multiple risk factors without established CVD.
Purpose of the Study:
- To examine contemporary clinical practice patterns of DAPT use after the CHARISMA trial publication.
- To compare DAPT prescription rates in patients with established CVD versus those with multiple risk factors but no established CVD.
Main Methods:
- Retrospective analysis of a large clinical registry from over 1000 physicians (2008-2011).
- Compared clinical characteristics and aspirin/clopidogrel prescription rates.
- Used multivariable Poisson regression to evaluate DAPT prescription trends over time.
Main Results:
- DAPT was prescribed to 20.5% of 167,839 patients with established CVD.
- DAPT was prescribed to 3.5% of 20,478 patients with multiple risk factors but no established CVD.
- DAPT prescription rates remained stable for established CVD patients but decreased significantly for multiple risk factor patients (IRR 0.77).
Conclusions:
- DAPT use is modest and stable in established CVD patients, aligning with CHARISMA subgroup findings.
- DAPT use is low and decreasing in patients with multiple risk factors only, consistent with CHARISMA's suggestion of potential harm.
Objectives:
CHARISMA was a landmark randomized clinical trial that failed to demonstrate a benefit of dual antiplatelet therapy (DAPT) over aspirin alone for preventing cardiovascular events. However, subgroup analyses of the trial found fewer major adverse cardiovascular events (MACEs) for patients with established cardiovascular disease but more MACEs for patients with multiple risk factors without established cardiovascular disease. Our objective was to examine DAPT use in contemporary clinical practice after publication of CHARISMA results.
Study Design:
Retrospective analysis of a large clinical registry of outpatient cardiovascular visits to over 1000 physicians that collected data on patient clinical history, symptoms, vital signs, and medications.
Methods:
Clinical characteristics and prescription rates of aspirin and clopidogrel were compared for patients with established cardiovascular disease and for patients with only multiple cardiovascular risk factors. Prescription of DAPT by calendar quarter was evaluated from 2008 to 2011 using multivariable Poisson regression models.
Results:
Of 167,839 patients with established cardiovascular disease, 20.5% were prescribed both aspirin and clopidogrel. Of 20,478 patients with multiple risk factors but no known cardiovascular disease, 3.5% were prescribed both aspirin and clopidogrel. Across 14 calendar quarters, prescription rates of DAPT did not change significantly for patients with established CVD but decreased for patients with multiple risk factors with an incidence rate ratio of 0.77.
Conclusions:
Use of DAPT is modest in patients with established cardiovascular disease, for whom the CHARISMA trial suggested decreased MACEs, and prescription rates have remained stable over time. Use of DAPT in patients with multiple risk factors only, for whom CHARISMA suggested that DAPT may lead to increased MACE, was low and decreased over time.
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