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One- versus three-month dual antiplatelet therapy in high bleeding risk patients undergoing percutaneous coronary
Davide Cao1,2, Pascal Vranckx3, Marco Valgimigli4,5
1Mount Sinai Heart, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Insights
Short dual antiplatelet therapy (DAPT) is safe for high bleeding risk patients after drug-eluting stent implantation. One month of DAPT, compared to three months, showed similar ischemic risk and reduced bleeding events at one year.
Area of Science:
- Cardiology
- Interventional Cardiology
- Clinical Trials
Background:
- Short dual antiplatelet therapy (DAPT) is a proposed strategy for patients at high bleeding risk (HBR) undergoing drug-eluting stent (DES) implantation.
- The safety and efficacy of abbreviated DAPT after non-ST-segment elevation acute coronary syndrome (NSTE-ACS) require further investigation.
Purpose of the Study:
- To compare the clinical outcomes of 1-month versus 3-month DAPT in HBR patients after DES implantation.
- To assess outcomes in both NSTE-ACS and non-NSTE-ACS patient subgroups.
Main Methods:
- Analysis of data from three prospective, international, single-arm studies (XIENCE Short DAPT programme).
- Evaluation of 1-month (XIENCE 28) versus 3-month (XIENCE 90) DAPT in HBR patients receiving cobalt-chromium everolimus-eluting stents.
- Propensity score stratification was used to compare ischemic and bleeding outcomes based on clinical presentation.
Main Results:
- In 3,364 HBR patients, 1-month DAPT showed similar rates of death or myocardial infarction compared to 3-month DAPT at 12 months, regardless of NSTE-ACS presence.
- Bleeding Academic Research Consortium (BARC) Type 2-5 bleeding was significantly reduced with 1-month DAPT in NSTE-ACS patients (HR 0.57) and showed a similar trend in stable patients (HR 0.84).
Conclusions:
- One-month DAPT is associated with similar ischemic risk and reduced bleeding compared to 3-month DAPT in HBR patients after everolimus-eluting stent implantation.
- This finding holds true irrespective of the patient's clinical presentation, including NSTE-ACS.
Background:
A short dual antiplatelet therapy (DAPT) duration has been proposed for patients at high bleeding risk (HBR) undergoing drug-eluting coronary stent (DES) implantation. Whether this strategy is safe and effective after a non-ST-segment elevation acute coronary syndrome (NSTE-ACS) remains uncertain.
Aims:
We aimed to compare the impact of 1-month versus 3-month DAPT on clinical outcomes after DES implantation among HBR patients with or without NSTE-ACS.
Methods:
This is a prespecified analysis from the XIENCE Short DAPT programme involving three prospective, international, single-arm studies evaluating the safety and efficacy of 1-month (XIENCE 28 USA and Global) or 3-month (XIENCE 90) DAPT among HBR patients after implantation of a cobalt-chromium everolimus-eluting stent. Ischaemic and bleeding outcomes associated with 1- versus 3-month DAPT were assessed according to clinical presentation using propensity score stratification.
Results:
Of 3,364 HBR patients (1,392 on 1-month DAPT and 1,972 on 3-month DAPT), 1,164 (34.6%) underwent DES implantation for NSTE-ACS. At 12 months, the risk of the primary endpoint of death or myocardial infarction was similar between 1- and 3-month DAPT in patients with (hazard ratio [HR] 1.09, 95% confidence interval [CI]: 0.71-1.65) and without NSTE-ACS (HR 0.88, 95% CI: 0.63-1.23; p-interaction=0.34). The key secondary endpoint of Bleeding Academic Research Consortium (BARC) Type 2-5 bleeding was consistently reduced in both NSTE-ACS (HR 0.57, 95% CI: 0.37-0.88) and stable patients (HR 0.84, 95% CI: 0.61-1.15; p-interaction=0.15) with 1-month DAPT.
Conclusions:
Among HBR patients undergoing implantation of an everolimus-eluting stent, 1-month, compared to 3-month DAPT, was associated with similar ischaemic risk and reduced bleeding at 1 year, irrespective of clinical presentation.
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