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Published on: May 14, 2013
Duration of dual antiplatelet therapy and risk of stent thrombosis in patients undergoing complex PCI: a
Fiorenzo Simonetti1,2, Claudia Carassia1, Hector Alfonso Alvarez Covarrubias1
1Klinik Für Herz- und Kreislauferkrankungen, TUM Klinikum Deutsches Herzzentrum, Technische Universität München, Munich, 80636, Germany.
Insights
For complex percutaneous coronary intervention (PCI), non-standard dual antiplatelet therapy (DAPT) durations did not significantly alter risks of stent thrombosis, myocardial infarction, death, or major bleeding compared to standard DAPT. These findings apply regardless of PCI complexity.
Area of Science:
- Cardiology
- Interventional Cardiology
- Clinical Trials
Background:
- Patients with complex percutaneous coronary intervention (PCI) face elevated ischemic event risks.
- Extended dual antiplatelet therapy (DAPT) is common for preventing stent thrombosis (ST) but balancing ischemic and bleeding risks is challenging.
- The impact of non-standard DAPT durations on outcomes in complex PCI is not well-established.
Purpose of the Study:
- To evaluate the effect of non-standard DAPT duration regimens on ischemic events in patients undergoing complex PCI.
- To compare the risks of stent thrombosis, myocardial infarction, all-cause death, and major bleeding between standard and non-standard DAPT durations in complex PCI.
Main Methods:
- A systematic search for randomized trials comparing DAPT duration strategies in complex PCI patients was conducted.
- Seven trials involving 46,696 patients (13,469 complex PCI) were included.
- Primary outcome was definite/probable stent thrombosis; secondary outcomes included myocardial infarction, all-cause death, and major bleeding.
Main Results:
- No significant difference in definite/probable ST risk was observed between non-standard and standard DAPT groups in complex PCI patients (IRR 1.08; 95% CI 0.63-1.82).
- Risks for myocardial infarction (IRR 0.87), all-cause death (IRR 0.85), and major bleeding (IRR 0.63) also showed no significant differences.
- The treatment effect on ST was independent of PCI complexity.
Conclusions:
- In complex PCI patients, varying DAPT durations did not lead to significant differences in stent thrombosis, myocardial infarction, death, or major bleeding.
- Current evidence suggests DAPT duration strategies may not critically impact key ischemic and bleeding outcomes in complex PCI settings.
Background:
Patients undergoing complex percutaneous coronary intervention (PCI) have a higher risk of ischemic events and often receive extended dual antiplatelet therapy (DAPT), particularly to protect against stent thrombosis (ST). The selection of an optimal DAPT strategy in this setting remains challenging given the intrinsic ischemic and bleeding risk. Previous observations have not clearly established the impact of non-standard DAPT duration regimens on ischemic events in complex PCI patients. This study aims to assess the effect of non-standard DAPT duration on ischemic events in this setting.
Methods And Results:
We searched for randomized trials comparing DAPT duration regimens in patients undergoing complex PCI. The primary outcome was definite/probable ST. Other outcomes were myocardial infarction (MI), all-cause death, and major bleeding. Seven trials with a total of 46,696 patients undergoing either complex (n = 13,469) or non-complex (n = 33,227) PCI were included in the analysis. In complex PCI patients, the risk of definite/probable ST was not significantly different between the non-standard DAPT and standard DAPT groups (incidence rate ratio (IRR) 1.08; 95% confidence intervals (CI) 0.63-1.82). Consistently, the risk of MI (IRR 0.87; 95% CI 0.70-1.09), all-cause death (IRR 0.85; 95% CI 0.51-1.39), and major bleeding (IRR 0.63; 95% CI 0.33-1.19) did not differ significantly between DAPT strategies. Treatment effect for definite/probable ST by DAPT duration strategy was independent of PCI complexity.
Conclusions:
In patients undergoing complex PCI, we found no significant differences in stent thrombosis, myocardial infarction, all-cause death, and major bleeding between DAPT duration strategies.
Prospero Registration Number:
CRD42024617534.
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