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Interventional Diagnostic Procedure: A Practical Guide for the Assessment of Coronary Vascular Function
Published on: March 15, 2022
Optimal aNtiplatelet pharmacotherapy guided by bedSIDE genetic or functional TESTing in elective PCI patients: A
Lukasz Koltowski1, Mariusz Tomaniak, Daniel Aradi
11st Department of Cardiology, Medical University of Warsaw, Poland, Poland. lukasz@koltowski.com.
Insights
Personalized dual antiplatelet therapy (DAPT) using genotyping or platelet function testing improves platelet inhibition in stable coronary artery disease patients after percutaneous coronary intervention. This approach may reduce cardiovascular risk by optimizing antiplatelet response.
Area of Science:
- Cardiology
- Pharmacogenomics
- Interventional Cardiology
Background:
- Dual antiplatelet therapy (DAPT) is standard after percutaneous coronary intervention (PCI) for stable coronary artery disease (SCAD).
- Suboptimal platelet inhibition affects one-third of patients, increasing cardiovascular risk.
- The ONSIDE TEST study investigated personalized DAPT strategies.
Purpose of the Study:
- To evaluate the clinical impact of personalized DAPT strategies in SCAD patients undergoing PCI.
- To assess the effectiveness of point-of-care genotyping and platelet function testing in guiding DAPT.
- To compare personalized DAPT with standard care regarding cardiovascular outcomes.
Main Methods:
- Fifty SCAD patients undergoing PCI were randomized into three groups: genotyping, platelet function testing (PFT), and control.
- Genotyping utilized the Spartan RX CYP2C19 System; PFT used the VerifyNow P2Y12 assay.
- Inadequate clopidogrel response prompted prasugrel administration; periprocedural myocardial injury (PMI) was the primary endpoint.
Main Results:
- Poor clopidogrel metabolizers were identified in 32% (genotyping arm) and 13% (PFT arm).
- Periprocedural platelet reactivity was significantly lower in the genotyping (80 ± 49.0 PRU) and PFT (36.5 ± 47 PRU) arms compared to control (176 ± 67.8 PRU).
- Periprocedural myocardial injury (PMI) occurred in 37% of the total study population.
Conclusions:
- Personalized DAPT strategies, guided by genotyping or PFT, enhance platelet inhibition in SCAD patients post-PCI.
- These personalized approaches are feasible for integration into clinical practice.
- Monitoring PMI rates is crucial for comparing DAPT strategies.
Background:
Dual antiplatelet therapy (DAPT) is recommended after elective percutaneous coronary intervention (PCI) in stable coronary artery disease (SCAD) patients; however, still one-third of patients do not obtain adequate platelet inhibition that may result in increased cardiovascular risk. The aim of the ONSIDE TEST study is to evaluate the clinical impact of point-of-care genotyping- and platelet function-based personalized dual antiplatelet strategies in SCAD individuals undergoing PCI.
Methods:
Fifty patients were randomized to one of the three study arms: 1) genotyping, 2) platelet function testing (PFT) and 3) control. Patients were tested with point-of-care Spartan RX CYP2C19 System (group 1) and VerifyNow P2Y12 assay (group 2). In cases of inadequate response to clopidogrel, a loading dose of prasugrel was administered before PCI. The main clinical endpoint is the incidence of periprocedural myocardial injury (PMI).
Results:
Five (32%) patients in the genotyping arm and two (13%) in the in the PFT arm were identi-fied as poor clopidogrel metabolizers. The periprocedural platelet reactivity was significantly lower in the genotyping (80 ± 49.0 PRU) and PFT (36.5 ± 47 PRU) arms as compared to the control arm (176 ± 67.8 PRU), p = 0.01 and p = 0.03, respectively. PMI appeared in 17 (37%) patients of the entire study population.
Conclusions:
Personalized DAPT results in an improved platelet inhibition. Apart from genotyping and aggregometry, it is feasible to integrate into everyday clinical practice PMI rates which are relevant when comparing different strategies.
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