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Published on: March 15, 2022
Short dual antiplatelet therapy duration after percutaneous coronary intervention in high bleeding risk patients:
Kevin R Bainey1, Guillaume Marquis-Gravel2, Blair J MacDonald3
1Mazankowski Alberta Heart Institute, University of Alberta, Edmonton, Alberta.
Insights
Short dual antiplatelet therapy (DAPT) for 1-3 months in high bleeding risk patients undergoing percutaneous coronary intervention (PCI) significantly reduces bleeding events. This shorter duration is safe, not increasing ischemic risks like MACE or stent thrombosis.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Pharmacology
Background:
- Dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI) is crucial for preventing stent thrombosis and major adverse cardiovascular events (MACE).
- Determining optimal DAPT duration is challenging, particularly for high bleeding risk (HBR) patients, where prolonged therapy increases bleeding complications.
Approach:
- A systematic review and meta-analysis of randomized controlled trials (RCTs) was conducted, including five RCTs with 7,242 patients.
- The study compared short DAPT (1-3 months) versus standard DAPT (6-12 months) in HBR patients post-PCI.
- Outcomes assessed included MACE, all-cause death, stent thrombosis, major bleeding, and clinically relevant non-major bleeding, with risk of bias and certainty of evidence evaluated.
Key Points:
- Short DAPT (1-3 months) did not increase the risk of MACE, all-cause death, or stent thrombosis compared to standard DAPT (6-12 months).
- Short DAPT significantly reduced major bleeding events (RR 0.34) and the composite of major or clinically-relevant non-major bleeding (RR 0.60).
- This translates to a reduction of 21 and 34 bleeding events per 1000 patients, respectively.
Conclusions:
- In high bleeding risk patients undergoing PCI, a DAPT duration of 1-3 months is effective in reducing bleeding events.
- Short DAPT can be safely implemented in HBR patients without compromising ischemic protection.
- Consideration of shorter DAPT durations is recommended for HBR patients receiving PCI.
Introduction:
Dual antiplatelet therapy (DAPT) following percutaneous coronary intervention (PCI) reduces major adverse cardiovascular events (MACE) and stent thrombosis. However, DAPT duration is a concern in high bleeding risk (HBR) patients. We evaluated the effect of short DAPT (1-3 months) compared to standard DAPT (6-12 months) on bleeding and ischemic events in HBR PCI.
Methods:
We searched MEDLINE, Embase and CENTRAL up to August 18, 2022. Randomized controlled trials (RCTs) comparing short DAPT (1-3 months) versus standard DAPT in HBR PCI were included. We assessed risk of bias (RoB) using the Cochrane RoB2 tool, and certainty of evidence using GRADE criteria. Outcomes included MACE, all-cause death, stent thrombosis, major bleeding, and the composite of major or clinically-relevant non-major bleeding. We estimated risk ratios (RR) and 95% confidence intervals (CI) using a random-effects model.
Results:
From 503 articles, we included five RCTs (n = 7,242) at overall low risk of bias with median follow-up of 12-months. Compared to standard DAPT, short DAPT did not increase MACE (RR 1.02, 95% CI 0.84-1.23), all-cause death (RR 0.92, 95% CI 0.71-1.20) or stent thrombosis (RR 1.47, 95% CI 0.73-2.93). Short DAPT reduced major bleeding (RR 0.34, 95% CI 0.13-0.90) and the composite of major or clinically-relevant non-major bleeding (RR 0.60, 95% CI 0.44-0.81), translating to 21 and 34 fewer events, respectively, per 1000 patients.
Conclusions:
In HBR PCI, DAPT for 1-3 months compared to 6-12 months reduced clinically-relevant bleeding events without jeopardizing ischemic risk. Short DAPT should be considered in HBR patients receiving PCI.
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