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A Murine Model of Stent Implantation in the Carotid Artery for the Study of Restenosis
Published on: May 14, 2013
Management of Restenosis after Stenting in Left Main Coronary Artery Disease
Chen-Wei Huang1, Mu-Shiang Huang1,2, Pei-Fang Su2
1Division of Cardiology, Department of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University.
Insights
For left main coronary artery disease with in-stent restenosis, drug-coated balloon angioplasty and new drug-eluting stents offer similar outcomes. Both treatments are viable alternatives to bypass surgery when it is not an option.
Area of Science:
- Interventional Cardiology
- Cardiovascular Research
- Medical Device Technology
Background:
- Optimal treatment for in-stent restenosis (ISR) in left main (LM) coronary artery disease, especially as an alternative to coronary artery bypass graft surgery (CABG), is not well-defined.
- Left main coronary artery disease poses significant risks, and managing ISR within this critical vessel requires careful consideration of treatment strategies.
Purpose of the Study:
- To compare the clinical effectiveness of a new drug-eluting stent (new-DES) strategy versus a drug-coated balloon (DCB) only strategy for treating left main in-stent restenosis (LM-ISR).
- To evaluate major adverse cardiovascular events (MACEs) and individual components in patients with LM-ISR unsuitable for CABG.
Main Methods:
- Retrospective analysis of intervention reports from a database, identifying patients with LM stents and subsequent LM-ISR.
- Patients were divided into two groups: new-DES implantation and DCB-only treatment.
- Comparison of composite MACEs and individual endpoints, including cardiovascular death, myocardial infarction, and target lesion revascularization, with additional meta-analysis of similar studies.
Main Results:
- No significant differences in MACEs (50.0% vs. 50.0%) were observed between the new-DES (n=40) and DCB-only (n=22) groups.
- Individual endpoints such as cardiovascular death, nonfatal myocardial infarction, and target lesion revascularization also showed no statistically significant differences between the groups.
- A meta-analysis of four similar studies corroborated the comparable MACE findings (odds ratio: 0.85, 95% CI: 0.44-1.67).
Conclusions:
- Both DCB angioplasty and repeat DES implantation are effective treatment options for LM-ISR lesions in patients not suitable for CABG.
- These interventions demonstrate comparable medium-term clinical results regarding MACEs, providing valuable insights for treatment decisions.
Background:
The optimal alternative treatment strategy to coronary artery bypass graft surgery (CABG) for in-stent restenosis (ISR) in left main (LM) coronary artery disease remains uncertain.
Methods:
We retrospectively screened all intervention reports from an intervention database and extracted those mentioning an LM stent. We then manually confirmed reports involving LM ISR and divided them into two groups, those in which the patient received a new drug-eluting stent (new-DES) strategy, and those in which the patient received a drug-coated balloon (DCB) only. A composite endpoint of major adverse cardiovascular events (MACEs) and each individual endpoint were compared. We also performed a brief analysis of similar designed studies.
Results:
Between the new-DES (n = 40) and DCB-only (n = 22) groups, during median respective follow-up times of 581.5 and 642.5 days, no significant statistical differences were detected in MACEs (50.0% vs. 50.0%, p = 0.974), cardiovascular death (27.5% vs. 13.6%, p = 0.214), nonfatal myocardial infarction (30.0% vs. 31.8%, p = 0.835), or target lesion revascularization (35.0% vs. 45.5%, p = 0.542). We analyzed four similar studies and found comparable MACE findings (odds ratio: 0.85, 95% CI: 0.44-1.67).
Conclusions:
Our findings support both DCB angioplasty and repeat DES implantation for LMISR lesions in patients who were clinically judged to be unsuitable for CABG; the treatments achieved comparable clinical results in terms of MACEs in the medium term.
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