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Dual antiplatelet therapy after percutaneous coronary intervention in patients at high bleeding risk: A systematic
Yan Han1, Xiaohang Yuan1, Xin Hu1
1Senior Department of Cardiology, Sixth Medical Center of Chinese PLA General Hospital, Beijing, China.
Insights
Shortening dual antiplatelet therapy (DAPT) to 3 months or less in high bleeding risk (HBR) patients after stenting reduces major bleeding events. This approach is safe and effective, with no significant increase in stent thrombosis or myocardial infarction risks.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacology
Background:
- Determining optimal dual antiplatelet therapy (DAPT) duration for high bleeding risk (HBR) patients post-percutaneous coronary intervention (PCI) remains unclear.
- This study investigates the safety and efficacy of short-term DAPT (≤ 3 months) in HBR patients receiving new-generation drug-eluting stents (DES).
Approach:
- A systematic review and meta-analysis of studies published up to November 2021.
- Included five observational studies and one randomized controlled trial, encompassing 15,432 HBR patients.
- Analyzed primary endpoints of major bleeding, stent thrombosis (ST), and myocardial infarction (MI), alongside secondary endpoints of all-cause death and ischemic stroke.
Key Points:
- Short DAPT (≤ 3 months) significantly reduced major bleeding compared to standard DAPT (> 3 months) in HBR patients (2.3% vs. 3.2%, p=0.03).
- No significant differences were observed in definite/probable ST (0.4% vs. 0.3%) or MI (2.4% vs. 2.0%) between short and standard DAPT durations.
- The findings suggest a favorable safety and efficacy profile for shorter DAPT durations in this patient cohort.
Conclusions:
- Short-term DAPT (≤ 3 months) is associated with reduced major bleeding in HBR patients with new-generation DES.
- This strategy does not significantly elevate the risks of stent thrombosis or myocardial infarction.
- Shortening DAPT duration is a viable option for managing HBR patients undergoing PCI.
Background:
To date, it has not been ascertained whether shortening the duration of dual antiplatelet therapy (DAPT) can benefit high bleeding risk (HBR) patients. This systematic review and meta-analysis was performed to investigate the safety and efficacy of short (≤ 3 months) DAPT in HBR patients after percutaneous coronary intervention (PCI).
Methods:
The PubMed, Embase, and Clinical Trials databases were searched from inception until November 2021 to identify studies that evaluated the safety and efficacy of short DAPT in HBR patients implanted with new-generation drug-eluting stents (DES). Primary endpoints included major bleeding, definite or probable stent thrombosis (ST), and myocardial infarction (MI), while secondary endpoints included all-cause death and ischemic stroke. Based on the fixed and random effect model, the risk ratio (RR) and 95% confidence interval of each endpoint were measured.
Results:
Five observational studies and one randomized controlled trial were included, involving 15,432 HBR patients. Short DAPT for HBR patients undergoing PCI had a lower incidence of major bleeding in comparison with standard (> 3 months) DAPT (2.3% vs. 3.2%, RR 0.64 [0.44, 0.95], p = 0.03), while short DAPT was comparable to standard DAPT with regard to definite or probable ST (0.4% vs. 0.3%, RR 1.31 [0.77, 2.23], p = 0.32) and MI (2.4% vs. 2.0%, RR 1.17 [0.95, 1.45], p = 0.14).
Conclusions:
Among HBR patients implanted with new-generation DES, short DAPT was associated with reduced risk of major bleeding without significantly increasing the risk of definite or probable ST and MI in comparison with standard DAPT.
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