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Updated: May 15, 2026

A Murine Model of Stent Implantation in the Carotid Artery for the Study of Restenosis
Published on: May 14, 2013
Five-year outcomes in patients with chronic total coronary occlusion treated with drug-eluting vs bare-metal stents:
Francesco De Felice1, Rosario Fiorilli, Antonio Parma
1UO Cardiologia Interventistica Azienda Ospedaliera S. Camillo Forlanini, Roma, Italy. f.defelice@lycos.com
Insights
Drug-eluting stents (DESs) significantly reduce major adverse cardiac events (MACE), target vessel failure (TVF), and target lesion revascularization (TLR) compared to bare-metal stents (BMS) in chronic total coronary occlusion (CTO) patients over 5 years.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Biomaterials Science
Background:
- Limited long-term data on drug-eluting stents (DESs) in chronic total coronary occlusion (CTO).
- Need to compare DES vs. bare-metal stents (BMS) for long-term safety and effectiveness in CTO.
- Previous studies focused on shorter follow-up periods.
Purpose of the Study:
- To evaluate the 5-year clinical outcomes of DES vs. BMS in patients with successfully treated CTO.
- To compare the incidence of major adverse cardiac events (MACE), target vessel failure (TVF), and target lesion revascularization (TLR) between DES and BMS groups.
- To identify predictors of MACE at 5-year follow-up.
Main Methods:
- Retrospective comparison of 156 patients treated with DES versus 159 historical controls treated with BMS.
- Primary endpoint: freedom from MACE (death, myocardial infarction, TLR).
- Secondary endpoints: freedom from TVF and TLR at 5 years.
Main Results:
- DES group showed significantly superior event-free survival from MACE (84% vs. 69%), TVF (71% vs. 84%), and TLR (77% vs. 92%) compared to BMS at 5 years.
- BMS vs. DES was an independent predictor of MACE (HR=3.37).
- Stent thrombosis rates were similar between groups (7% DES vs. 4% BMS).
Conclusions:
- Drug-eluting stents (DESs) are superior to bare-metal stents (BMSs) in reducing MACE, TVF, and TLR in CTO patients at 5-year follow-up.
- DESs should be the preferred treatment strategy for CTO.
- Long-term outcomes favor DES implantation in complex coronary artery disease.
Background:
Limited data exist on long-term safety and effectiveness of drug-eluting stents (DESs) in true chronic total coronary occlusion (CTO) settings. We evaluated 5-year clinical outcomes of patients with CTO treated successfully with DES vs bare-metal stent (BMS).
Methods:
We compared the 5-year clinical outcomes of 156 patients treated with DES implantation with outcomes of a historical cohort of 159 patients treated with BMS. Primary end point was freedom from major adverse cardiac events (MACEs; defined as death, myocardial infarction [MI], and target lesion revascularization [TLR]); secondary end points were freedom from target vessel failure (TVF; combination of target vessel revascularization, MI, and cardiac death) and TLR at 5 years.
Results:
After 5 years, the DES group had significantly superior event-free survival from MACE (84% vs 69%; log rank P < 0.001), TVF (71% vs 84%; P = 0.002), and TLR (77% vs 92%; P = 0.0001), compared with the BMS group. The Cox proportional hazards model identified BMS vs DES (adjusted hazard ratio [HR] = 3.37; 95% confidence interval [CI], 1.85-6.17; P = 0.001), final minimal lumen diameter (HR, 0.27; 95% CI, 0.14-0.52; P = 0.0001), and stent length (HR, 1.01; 95% CI, 1.00-1.03; P = 0.03) as independent predictors of MACE at 5-year follow-up. Twelve (7%) and 7 (4%) stent thromboses occurred in the DES and BMS groups (P = 0.23), respectively.
Conclusions:
After 5 years, DESs were superior to BMSs in reducing MACE, TVF, and TLR in patients with CTO and should be the preferred strategy.
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