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The underutilisation of dual antiplatelet therapy in acute coronary syndrome
Malcolm Anastasius1, Jerrett K Lau1, Karice Hyun2
1Department of Cardiology, Concord Repatriation General Hospital, University of Sydney, Sydney, Australia.
Insights
Dual antiplatelet therapy (DAPT) is underutilized in acute coronary syndrome (ACS) despite guidelines. This study identified patient subgroups not receiving DAPT, highlighting a treatment gap needing intervention.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Medicine
Background:
- Dual antiplatelet therapy (DAPT) is recommended for acute coronary syndrome (ACS) but is underutilized.
- Identifying predictors of DAPT non-prescription is crucial for improving patient outcomes.
Purpose of the Study:
- To determine independent predictors of DAPT non-prescription in ACS patients.
- To describe patterns of DAPT prescription over time in ACS management.
Main Methods:
- Analysis of 8939 ACS patients from 41 Australian hospitals (2009-2016).
- Stratification by discharge antiplatelet therapy: DAPT, single antiplatelet therapy (SAPT), or no antiplatelet therapy.
- Multivariable logistic regression used to identify predictors of DAPT non-prescription.
Main Results:
- 70.4% of ACS patients received DAPT at discharge; 24.1% received SAPT, and 5.5% received no antiplatelet therapy.
- In-hospital CABG, warfarin use, major bleeding, unstable angina, NSTEMI, atrial arrhythmia, hypertension, and high GRACE risk were predictors of DAPT non-prescription.
- DAPT prescription increased from 2013-2016, with a shift towards ticagrelor over clopidogrel, but no overall change in DAPT frequency across the study period.
Conclusions:
- High-risk ACS subgroups are identified as not receiving optimal DAPT.
- Strategies are needed to address the treatment gap in antiplatelet management for ACS patients.
Background:
Despite guideline recommendation of dual antiplatelet therapy (DAPT) in treating ACS, DAPT is underutilized. Our objective was to determine independent predictors of DAPT non-prescription in ACS and describe pattern of DAPT prescription over time.
Methods:
Patients presenting to 41 Australian hospitals with an ACS diagnosis between 2009 and 2016 were stratified according to discharge prescription with DAPT and single antiplatelet therapy (SAPT) or no antiplatelet therapy. Multiple stepwise logistic regression, accounting for within hospital clustering, was used to determine the independent predictors of DAPT non-prescription, defined as discharge with SAPT alone or no antiplatelet agent.
Results:
8939 patients survived to discharge with an ACS diagnosis. Of these, 6294 (70.4%) patients were discharged on DAPT, 2154 (24.1%) on SAPT and 491 (5.5%) on no antiplatelet agent. Independent predictors of DAPT non-prescription in the overall cohort were: in-hospital CABG (OR 0.09, 95%CI 0.05-0.14), discharge with warfarin (0.10 (0.07-0.14)), in hospital major bleeding (0.48 (0.34-0.67), diagnosis of unstable angina (0.35, (0.27-0.45)), non-ST-elevation myocardial infarction (0.67 (0.57-0.78)) [both vs. ST-segment elevation myocardial infarction], in hospital atrial arrhythmia (0.72 (0.60-0.86)), history of hypertension (0.83 (0.73-0.94)) and GRACE high risk (0.83 (0.71-0.98)). There was an increase in prescription of DAPT and a shift towards ticagrelor over clopidogrel for ACS from 2013 to 2016 (p<0.0001), but no overall change in the frequency of DAPT prescription over the entire study period.
Conclusion:
This study revealed high-risk ACS subgroups who do not receive optimal DAPT. Strategies are necessary to bridge the treatment gap in ACS antiplatelet management.
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