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Fibrinolytic therapy for very late stent thrombosis--is it a viable option?
Abdul Hakeem1, Sabha Bhatti, Imran Arif
1Division of Cardiovascular Diseases, College of Medicine, University of Cincinnati, Cincinnati, OH 45257-0542, USA. ahakeem@gmail.com
Insights
Very late stent thrombosis (ST) carries high mortality. Fibrinolytic therapy may be a viable option for ST-related ST-elevation myocardial infarction (STEMI) when primary percutaneous coronary intervention (PCI) is unavailable.
Area of Science:
- Cardiology
- Interventional Cardiology
- Biomedical Engineering
Background:
- Stent thrombosis (ST) is a serious complication following coronary stent placement, associated with high mortality and morbidity.
- Drug-eluting stents (DES) show an increased risk of very late ST compared to bare-metal stents up to 4 years post-implantation.
- Discontinuation of antiplatelet therapy, specifically clopidogrel, is a primary risk factor for ST.
Observation:
- ST-elevation myocardial infarction (STEMI) secondary to ST presents with worse outcomes and lower reperfusion rates than de novo STEMI.
- Prompt revascularization is critical for STEMI due to ST, given its significantly higher associated mortality.
- This case highlights the potential role of fibrinolytic therapy in managing STEMI caused by very late ST.
Findings:
- Very late stent thrombosis (ST) is associated with significant risks, particularly with drug-eluting stents (DES).
- Discontinuation of clopidogrel is the most critical risk factor for stent thrombosis.
- Fibrinolytic therapy demonstrated potential utility in a case of STEMI due to very late ST.
Implications:
- Systemic fibrinolysis should be considered for ST-related STEMI in cases of ongoing ischemia where prompt percutaneous coronary intervention (PCI) is not feasible.
- This approach may improve outcomes in specific high-risk scenarios of stent thrombosis.
- Further research into the role of fibrinolysis for very late ST is warranted.
Abstract:
Stent thrombosis (ST) has a very high case fatality and morbidity rates. The risk of very late ST is significantly increased with drug-eluting stents (DES) compared to bare-metal stents for at least up to 4 years. Discontinuation of clopidogrel therapy is the single most important consistently identified risk factor. Immediate reperfusion, preferably by primary percutaneous coronary intervention (PCI), has been considered the therapy of choice. Compared to de novo ST-elevation myocardial infarction (STEMI), myocardial infarction (MI) related to ST has significantly higher major adverse cardiovascular events (MACE) and lower reperfusion rates. Due to the significantly higher mortality associated with STEMI due to ST, prompt revascularization assumes paramount significance. Our case reflects the potential utility of fibrinolytic therapy for STEMI due to very late ST. Systemic fibrinolysis should be considered for ST in the presence of ongoing significant ischemia and unavailability of prompt PCI.
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