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Short dual antiplatelet therapy in patients with high bleeding risk undergoing percutaneous coronary intervention: a
Junyan Zhang1, Zhongxiu Chen1, Chen Li1
1Department of Cardiology, West China Hospital of Sichuan University, Chengdu, China.
Insights
Shortening dual antiplatelet therapy (DAPT) to 1 or 6 months is safe for high bleeding risk patients after PCI. A 6-month DAPT regimen reduces bleeding risk without increasing major adverse cardiac events.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacology
Background:
- Dual antiplatelet therapy (DAPT) duration after percutaneous coronary intervention (PCI) in high bleeding risk (HBR) patients is debated.
- Optimizing DAPT duration is crucial to balance ischemic and bleeding risks.
Purpose of the Study:
- To evaluate the efficacy and safety of abbreviated DAPT durations in HBR patients undergoing PCI.
- To compare short-term DAPT regimens (1, 3, and 6 months) against longer durations regarding clinical outcomes.
Main Methods:
- A systematic literature search was conducted across major databases (Cochrane, PubMed, EMBASE, Ovid MEDLINE).
- Meta-analysis of nine studies (10 cohorts) involving PCI-HBR patients comparing different DAPT durations.
- Outcomes assessed included major adverse cardiac events (MACE) and net adverse clinical events (NACE).
Main Results:
- One-month DAPT showed comparable risks of NACE and MACE versus longer durations (>1 month).
- Three-month DAPT did not increase MACE but elevated risks of ischemic stroke and stent thrombosis compared to >3 months.
- Six-month DAPT reduced major bleeding risk without increasing NACE or MACE compared to >6 months.
Conclusions:
- Shortened DAPT to 1 or 6 months is associated with comparable MACE risk in PCI-HBR patients.
- A 6-month DAPT regimen effectively reduces major bleeding risk.
- While generally beneficial, a 3-month DAPT regimen showed an increased risk of ischemic stroke.
Background:
The efficacy and safety of an abbreviated duration of dual antiplatelet therapy (DAPT) in patients with high bleeding risk (HBR) undergoing percutaneous coronary intervention (PCI) (PCI-HBR patients) remain controversial.
Methods:
The Cochrane Library, PubMed, EMBASE, and Ovid MEDLINE databases were searched. Studies that enrolled PCI-HBR patients as research subjects, compared different DAPT durations, and reported incidences of major adverse cardiac events (MACE) and net adverse clinical events (NACE) in PCI-HBR patients were obtained. The studies were stratified according to the DAPT duration (1, 3, and 6 months), and meta-analysis was subsequently performed.
Results:
Nine studies (10 cohorts) were included in the meta-analysis. Compared with those who received DAPT for >1 month, PCI-HBR patients who received the 1-month DAPT regimen had comparable risks of NACE and MACE. Compared to those who received DAPT for >3 months, the risk of developing MACE in PCI-HBR patients who received the 3-month DAPT was not increased; however, the risk of ischemic stroke and stent thrombosis increased. Compared to those who received DAPT for >6 months, patients who received the 6-month DAPT had a reduction in the risk of major bleeding without an increase in NACE and MACE.
Conclusions:
Shortening the DAPT regimen to 1 or 6 months did not increase the risk of MACE, and the 6-month DAPT regimen reduced the risk of major bleeding. However, the 3-month DAPT regimen increased the risk of ischemic stroke. Thus, shortened DAPT reduced the risk of MACE and bleeding, with a small absolute increase in ischemic strokes.
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