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Real-world five-year outcomes of FlexyRap ® cobalt-chromium rapamycin-eluting stents with biodegradable polymer in patients with de-novo coronary artery disease.
- Source :
-
World journal of cardiology [World J Cardiol] 2023 Mar 26; Vol. 15 (3), pp. 84-94. - Publication Year :
- 2023
-
Abstract
- Background: The use of biodegradable polymer drug-eluting stents (BP-DES) has been proven to minimize restenosis and stent thrombosis. The current post-marketing monitoring was observed at the 5-year clinical outcomes of individuals who had been treated with FlexyRap <superscript>®</superscript> DES in the real world.<br />Aim: To assess the safety and effectiveness of FlexyRap <superscript>®</superscript> DES at the 5-year follow-up in real-world settings.<br />Methods: Findings from a retrospective, multi-center, observational, post-market clinical follow-up study of patients treated with FlexyRap <superscript>®</superscript> DES for de novo coronary artery disease (CAD) were reported. During the 12-mo follow-up, the primary endpoint was target lesion failure, which was defined as the composite of cardiovascular death, target vessel myocardial infarction (TV-MI), and clinically driven target lesion revascularization.<br />Results: The data of 500 patients received with FlexyRap <superscript>®</superscript> DES was obtained at the completion of the surveillance timeline of 5-year. After the implantation of FlexyRap <superscript>®</superscript> DES, the device success rate was 100%. Adverse events that led to major bleeding, permanent disability, or death were not experienced in the patients. The major adverse cardiac event rate at 12-mo, 3-year, and 5-year follow-up was 1 (0.2%), 0 (0%), and 1 (0.2%) respectively with 0 (0%) cardiovascular death, 2 (0.4%) TV-MI, and 0 (0%) TLR compositely. Furthermore, late stent thrombosis was found in 2 (0.4%) patients at the follow-up of 12-mo, very late stent thrombosis was observed in 2 patients (0.4%) at 3-year follow-up.<br />Conclusion: FlexyRap <superscript>®</superscript> DES was proved to be safe and efficacious in real-world patients with de novo CAD, indicating a lowered rate of cardiac events and stent thrombosis at 5-year follow-up.<br />Competing Interests: Conflict-of-interest statement: Ms. Preeti and Dr. Malte are employees of Sahajanand Laser Technology Ltd. (SLTL), India. All other authors have nothing to disclose.<br /> (©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved.)
Details
- Language :
- English
- ISSN :
- 1949-8462
- Volume :
- 15
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- World journal of cardiology
- Publication Type :
- Academic Journal
- Accession number :
- 37033681
- Full Text :
- https://doi.org/10.4330/wjc.v15.i3.84