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Updated: Jul 13, 2026

A Murine Model of Stent Implantation in the Carotid Artery for the Study of Restenosis
Published on: May 14, 2013
Late and very late thrombosis of drug-eluting stents: evolving concepts and perspectives
Ronen Jaffe1, Bradley H Strauss
1Schulich Heart Program, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.
Insights
Drug-eluting stents (DES) reduce restenosis but may increase late stent thrombosis risk compared to bare-metal stents (BMS). Ongoing research investigates optimal dual antiplatelet therapy duration and novel stent designs to mitigate this risk.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Biomaterials Science
Background:
- Coronary stents are crucial for percutaneous coronary revascularization, improving outcomes by reducing vessel closure and restenosis.
- Stent thrombosis (ST), though rare, is a severe complication of percutaneous coronary intervention (PCI), potentially leading to myocardial infarction and sudden death.
- Advances in stent implantation and dual antiplatelet therapy (DAPT) have significantly lowered ST rates.
Purpose of the Study:
- To review the pathophysiology of late drug-eluting stent (DES) thrombosis.
- To discuss the current understanding and ongoing controversies surrounding the incremental risk of ST with DES compared to bare-metal stents (BMS).
- To explore the role of DAPT duration and novel stent designs in managing ST.
Main Methods:
- Literature review of studies comparing BMS and DES regarding stent thrombosis.
- Analysis of data on the incidence and timing of ST in different stent types.
- Discussion of clinical significance and risk factors for late DES thrombosis.
Main Results:
- Bare-metal stent (BMS) thrombosis occurs in <1% of cases, typically within the first month.
- Concerns exist regarding late ST with drug-eluting stents (DES), particularly in complex lesions not studied in initial trials.
- Recent data suggest a potential 0.5% increased long-term thrombosis risk with DES, though clinical significance is debated.
Conclusions:
- While DES have improved revascularization, late ST remains a concern, especially in complex subsets.
- Optimal DAPT duration and novel stent designs are critical areas for future research to minimize ST risk.
- Further understanding of late DES thrombosis pathophysiology is needed.
Abstract:
Coronary stents are the mainstay of percutaneous coronary revascularization procedures and have significantly decreased the rates of acute vessel closure and restenosis. Stent thrombosis (ST) after percutaneous coronary intervention is an uncommon and potentially catastrophic event that might manifest as myocardial infarction and sudden death. Optimization of stent implantation and dual antiplatelet therapy have markedly reduced the occurrence of this complication. Bare-metal stent (BMS) thrombosis occurs in <1% of the cases, usually within the first month after implantation. The advent of drug-eluting stents (DES) has raised concerns regarding later occurrence of ST, beyond the traditional 1-month timeframe, especially in complex lesion subsets that were excluded from randomized trials that compared BMS to DES. There is widespread controversy regarding the actual incremental risk associated with DES. Recent studies suggest a 0.5% increased long-term thrombosis risk with DES; however, the clinical significance of these events remains under debate. The degree of protection achieved by dual antiplatelet therapy and optimal duration of treatment are under investigation. Novel stent designs might potentially decrease the incidence of this event. In this review, we will describe the current knowledge of the pathophysiology of late DES thrombosis, although many aspects remain incompletely understood.
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