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Effectiveness and Safety of Zotarolimus-Eluting Stent (Resolute™ Integrity) in Patients with Diffuse Long Coronary
Keun Ho Park1, Youngkeun Ahn2, Young Youp Koh1
1Division of Cardiology, Department of Internal Medicine, Chosun University Hospital, Gwangju, Korea.
Insights
Resolute™ zotarolimus-eluting stents (R-ZES) show excellent 1-year outcomes for diffuse long coronary artery disease (DLCAD) patients in Korea. The study found low rates of major adverse cardiac events (MACE) and stent thrombosis.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Biomedical Engineering
Background:
- Diffuse long coronary artery disease (DLCAD) presents challenges with unfavorable outcomes post-percutaneous coronary intervention (PCI).
- Evaluating novel stent technologies is crucial for improving DLCAD management.
- The Resolute™ zotarolimus-eluting stent (R-ZES) offers a potential solution for complex coronary lesions.
Purpose of the Study:
- To assess the effectiveness and safety of the Resolute™ zotarolimus-eluting stent (R-ZES) in patients with DLCAD.
- To determine the 12-month incidence of major adverse cardiac events (MACE) following R-ZES implantation for DLCAD.
- To identify predictors of MACE in this patient cohort.
Main Methods:
- A prospective study involving 1,011 patients undergoing PCI with R-ZES for lesions >25 mm in Korea (December 2011-December 2014).
- Major adverse cardiac events (MACE) were defined as cardiac death, non-fatal myocardial infarction, or target vessel revascularization.
- Clinical outcomes were analyzed at 12 months post-procedure.
Main Results:
- The study included a significant cohort with a mean age of 63.8 years, predominantly male (69.3%), with high rates of hypertension (87.0%) and multi-vessel disease (53.9%).
- A total of 1,697 R-ZES were implanted in 1,472 lesions, with overlapping stents used in 13.8% of cases.
- The 12-month incidence of MACE was 3.0%, and definite stent thrombosis was 0.3%. Independent predictors of MACE included multiple overlapping stents, prior heart failure, multi-vessel disease, and age ≥75 years.
Conclusions:
- The Resolute™ zotarolimus-eluting stent (R-ZES) demonstrates excellent 1-year clinical outcomes in Korean patients with diffuse long coronary artery disease (DLCAD).
- The safety and efficacy profile of R-ZES supports its use in managing complex coronary artery lesions.
- Identifying predictors of MACE can aid in risk stratification and personalized treatment strategies for DLCAD patients.
Background And Objectives:
Diffuse long coronary artery disease (DLCAD) still has unfavorable clinical outcomes after successful percutaneous coronary intervention (PCI). Therefore, we aimed to evaluate the effectiveness and safety of Resolute™ zotarolimus-eluting stent (R-ZES; Resolute™ Integrity) for patients with DLCAD.
Methods:
From December 2011 to December 2014, 1,011 patients who underwent PCI using R-ZES for CAD with longer than 25 mm lesion were prospectively enrolled from 21 hospitals in Korea. We assessed the clinical outcome of major adverse cardiac events (MACE) defined as the composite of cardiac death, non-fatal myocardial infarction (MI), and clinically-driven target vessel revascularization at 12 months.
Results:
Mean age was 63.8±10.8 years, 701 (69.3%) patients were male, 572 (87.0%) patients had hypertension, 339 (33.8%) patients had diabetes, 549 (54.3%) patients diagnosed with acute MI and 545 (53.9%) patients had multi-vessel disease (MVD). A total of 1,697 stents were implanted into a total of 1,472 lesions. The mean diameter was 3.07±0.38 mm and the length was 28.27±6.97 mm. Multiple overlapping stents were performed in 205 (13.8%) lesions. A 12-month clinical follow-up was available in 1,004 patients (99.3%). The incidences of MACE and definite stent thrombosis at 12-month were 3.0% and 0.3% respectively. On multivariate Cox-regression analysis, multiple overlapping stents implantation, previous congestive heart failure, MVD, and age ≥75 years were independent predictors of one-year MACE.
Conclusions:
Our study shows that R-ZES has an excellent 1-year clinical outcome in Korean patients with DLCAD.
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