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Updated: Jun 2, 2026

A Murine Model of Stent Implantation in the Carotid Artery for the Study of Restenosis
Published on: May 14, 2013
[Coronary stent thrombosis: what's new in 2011?]
M Oberhänsli1, S Puricel, M Togni
1Cardiology, University Fribourg, Schweiz.
Insights
Stent thrombosis (ST), a complication of percutaneous coronary interventions (PCI), has high mortality. Optimizing dual antiplatelet therapy and using newer agents can reduce ST risk.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
Context:
- Stent thrombosis (ST) is a critical complication following percutaneous coronary interventions (PCI), associated with significant mortality.
- Both bare metal stents (BMS) and drug-eluting stents (DES) exhibit comparable rates of early and late ST.
- Very late ST is a distinct concern with first-generation DES, linked to healing issues and hypersensitivity.
Purpose:
- To review the incidence, predictors, and prevention strategies for stent thrombosis.
- To highlight the role of dual antiplatelet therapy (DAPT) and emerging pharmacologic agents in mitigating ST risk.
Summary:
- ST occurs early, late, and very late after PCI, with rates varying by stent type and time post-procedure.
- Key predictors include inadequate platelet inhibition, procedural complications (e.g., stent underexpansion), and patient factors (e.g., diabetes, renal failure).
- Premature DAPT cessation and clopidogrel resistance are significant ST risk factors, while newer agents like prasugrel and ticagrelor offer improved outcomes.
Impact:
- Understanding ST predictors and risk factors is crucial for optimizing patient management after PCI.
- The introduction of novel antiplatelet agents promises to further reduce the incidence of ST.
- Improved prevention strategies can lead to better long-term outcomes for patients undergoing coronary interventions.
Abstract:
Stent thrombosis (ST) is a serious complication of percutaneous coronary interventions (PCI) with high mortality rates of up to 45%. Bare metal stents (BMS) and drug-eluting stents (DES) present similar rates of early (0.6%-1.2%) and late (0.3%-0.4%) ST. Very late ST is a specific entity after implantation of first-generation DES (sirolimus and paclitaxel) with an observed rate at 0.6% events/year. Strong predictors for early and late ST include: inadequate platelet inhibition, acute coronary syndromes (ACS), procedure-related factors such as stent underexpansion or dissection and patient-related factors such as diabetes, renal failure or a low left ventricular ejection fraction. Very late ST has been associated with delayed endothelial healing and drug-induced hypersensitivity reaction with exaggerated positive vessel remodeling, secondary incomplete stent apposition and paradoxical vasoconstriction. Dual antiplatelet therapy plays a key role in the prevention of ST. Premature dual antiplatelet therapy interruption (<6 months after PCI) and clopidogrel resistance (25% of patients) are strongly associated with ST. Finally, promising new pharmacologic agents such as prasugrel and ticagrelor have been introduced, permitting more predictable inhibition of platelet aggregation and enabling a further reduction in ST risk.
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