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Published on: January 21, 2020
Novel ultra-long (48 mm) everolimus-eluting stent for diffusely coronary vessels disease
Lorenzo Genuardi1, Francesco Burzotta2, Giulio Russo1
1Institute of Cardiology, A. Gemelli IRCCS University Policlinic Foundation, Sacred Heart Catholic University, Rome, Italy.
Insights
Ultra-long drug-eluting stents show promising results in treating diffuse coronary artery disease, reducing the need for stent overlaps during percutaneous coronary intervention (PCI). This real-world study found a 7% device-oriented composite endpoint rate in patients treated with 48 mm everolimus-eluting stents.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Biomedical Engineering
Background:
- Diffuse coronary artery disease often requires overlapping stents, increasing risks.
- Novel ultra-long drug-eluting stents (DES) aim to minimize stent overlap.
- Everolimus-eluting stents (EES) are a type of DES used in percutaneous coronary intervention (PCI).
Purpose of the Study:
- To evaluate the clinical outcomes of PCI using a novel 48 mm EES in a real-world population.
- To assess the effectiveness of ultra-long EES in reducing stent overlaps for diffuse coronary disease.
- To identify factors influencing device-oriented composite endpoint (DOCE) after PCI with ultra-long EES.
Main Methods:
- A real-world cohort of 216 patients undergoing PCI with 48 mm EES was analyzed.
- Patients were treated between June 2015 and April 2017, excluding those in cardiogenic shock.
- Vessels were categorized as "very long lesion" or "multiple focal disease"; DOCE was the primary endpoint.
Main Results:
- 230 vessels in 216 patients were treated; 43.9% required overlapping stents.
- The median follow-up was 474 days, with a 7% DOCE rate and no stent thrombosis.
- Diabetes was associated with increased DOCE, while "multiple focal disease" predicted lower DOCE.
Conclusions:
- The use of ultra-long EES in real-world practice shows promising results for diffuse coronary disease.
- These stents may effectively limit the need for stent overlaps during PCI.
- Further research can explore long-term outcomes and specific patient subgroups.
Background:
Long drug-eluting stents may limit the need of stent overlaps in patients with diffusely diseased coronary arteries. We evaluated the clinical results of percutaneous-coronary-intervention (PCI) using a novel ultra-long (48 mm) everolimus-eluting stent (EES) in a real-word population.
Methods:
Patients who underwent PCI with 48 mm EES between June 2015 and April 2017 in our Center were enrolled. The only exclusion criteria was cardiogenic shock established before PCI. Target vessels were divided in "very long lesion" (>38 mm) and "multiple focal disease" (multiple stenoses separated by healthy coronary segments >10 mm). Clinical follow-up was obtained to evaluate the occurrence of device-oriented composite endpoint (DOCE) (primary end-point).
Results:
A total of 216 patients were identified (70.6±11 years, 48.1% acute coronary syndrome) who were treated on 230 vessels. The target vessel appearance was "very long lesion" in 44.8% of cases and "multiple focal disease" in 55.2%. A single 48-mm EES was implanted in 129 (56.1%), while additional overlapping stents were needed in 101 cases (43.9%). Total stent length was 64.9±24.0 mm. The median follow-up time was of 474 (411-614) days, DOCE occurred in 7% of patients. No stent thrombosis was noticed. At multivariate analysis, diabetes was associated with DOCE increase (P=0.02), while "multiple focal disease" predicted lower DOCE (P=0.02).
Conclusions:
The present real-world experience shows promising clinical results with the use of ultra-long stents in order to limit the need of stents overlaps in patients with diffuse coronary disease undergoing PCI.
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