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Interventional Diagnostic Procedure: A Practical Guide for the Assessment of Coronary Vascular Function
Published on: March 15, 2022
Dual antiplatelet therapy after percutaneous coronary intervention for left main coronary artery disease
Sungsoo Cho1, Do-Yoon Kang2, Jung-Sun Kim3
1Department of Cardiology, Heart and Brain Hospital, Chung-Ang University Gwangmyeong Hospital, Chung-Ang University College of Medicine, Gwangmyeong, Gyeonggi-do, Republic of Korea.
Insights
Dual antiplatelet therapy (DAPT) duration after left main coronary artery (LMCA) percutaneous coronary intervention (PCI) varies. Shorter DAPT (<12 months) is linked to increased major adverse cardiovascular events (MACE), while bleeding risk remains similar across durations.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Clinical Trials
Background:
- Limited data exist on optimal dual antiplatelet therapy (DAPT) duration post-percutaneous coronary intervention (PCI) for left main coronary artery (LMCA) disease.
- Second-generation drug-eluting stents are commonly used, necessitating understanding of DAPT's long-term impact.
Purpose of the Study:
- To investigate DAPT duration patterns in patients undergoing PCI for LMCA disease.
- To evaluate the prognostic effect of varying DAPT durations on cardiovascular events and bleeding.
Main Methods:
- Analysis of individual patient data from IRIS-MAIN and KOMATE registries.
- Inclusion of 1827 patients treated with second-generation drug-eluting stents for LMCA disease.
- Assessment of major adverse cardiovascular events (MACE) and TIMI major bleeding.
Main Results:
- DAPT durations varied: <6 months (n=273), 6-12 months (n=477), 12-24 months (n=637), ≥24 months (n=440).
- Prolonged DAPT was associated with reduced MACE incidence.
- Patients with DAPT <6 months and 6-12 months had significantly higher MACE risk compared to 12-24 months (adjusted HRs 4.51 and 1.92, respectively).
- No significant difference in major bleeding was observed across DAPT duration groups.
Conclusions:
- DAPT duration after LMCA PCI is inconsistent.
- DAPT durations shorter than 12 months are associated with an increased risk of MACE.
- Individual patient clinical context is crucial when determining DAPT duration.
Introduction And Objectives:
There are scarce data on the optimal duration and prognostic impact of dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI) with second-generation drug-eluting stents for left main coronary artery (LMCA) disease. The aim of this study was to investigate the practice pattern and long-term prognostic effect of DAPT duration in patients undergoing PCI with second-generation drug-eluting stents for LMCA disease.
Methods:
Using individual patient-level data from the IRIS-MAIN and KOMATE registries, 1827 patients undergoing PCI with second-generation drug-eluting stents for LMCA disease with valid information on DAPT duration were included. The efficacy outcome was major adverse cardiovascular events (MACE, a composite of cardiac death, myocardial infarction, and stent thrombosis) and the safety outcome was TIMI major bleeding.
Results:
DAPT duration was <6 months (n=273), 6 to 12 months (n=477), 12 to 24 months (n=637), and ≥ 24 months (n=440). The median follow-up duration was 3.9 [interquartile range, 3.01-5.00] years. Prolonged DAPT duration was associated with lower incidences of MACE. In multigroup propensity score analysis, adjusted HR for MACE were significantly higher for DAPT <6 months and DAPT 6 to 12 months than for DAPT 12 to 24 months (HR, 4.51; 95%CI, 2.96-6.88 and HR 1.92; 95%CI, 1.23-3.00). There was no difference in HR for major bleeding among the assessed groups.
Conclusions:
DAPT duration following PCI for LMCA disease is highly variable. Although the duration of DAPT should be considered in the context of the clinical situation of each patient, <12 months of DAPT was associated with higher incidence of MACE. Registration identifiers: NCT01341327; NCT03908463.
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