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First in human evaluation of a novel Sirolimus-eluting ultra-high molecular weight bioresorbable scaffold: 9-, 24-and 36-months imaging and clinical results from the multi-center RENASCENT study.
- Source :
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International journal of cardiology [Int J Cardiol] 2020 Dec 15; Vol. 321, pp. 48-53. Date of Electronic Publication: 2020 Aug 15. - Publication Year :
- 2020
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Abstract
- Background: RENASCENT is a prospective, multi-center first-in-human clinical study to evaluate the clinical performance of the novel sirolimus-eluting 150-μm strut thickness FORTITUDE® BRS for percutaneous coronary intervention of single de novo coronary lesions.<br />Methods: FORTITUDE® BRS was tested in a prospective study in Italy and Colombia. Study objectives were in-scaffold angiographic late lumen loss (LLL) measured by quantitative coronary angiography and target vessel failure (TVF) defined as the composite rate of cardiac death, target vessel myocardial infarction or ischemia driven target lesion revascularization (TLR) at 9- and 24-months with clinical results up to 36-months.<br />Results: A total of 63 patients were enrolled. All patients underwent lesion pre-dilatation and 22 patients (34.9%) underwent post-dilatation. Clinical device and procedural success was 98.4% (62/63 patients) and 96.8% (61/63 patients) respectively. At 9-months, TVF occurred in 3/61 (4.9%) of the patients including 2 peri-procedural MI and one ischemia-driven TLR. Between 9- to 24-months, ischemia-driven TLR occurred in 3 additional patients (4.9%) including 1 patient who presented with very late ST after stopping all medications. There were no further TVF between 24- and 36-months.<br />Conclusions: In this multi-center prospective study, the FORTITUDE® BRS was shown to be safe and effective in the treatment of single coronary lesions with low levels of TVF and LLL at 9- and 24-months. It was shown to be clinically safe upto 36-months follow-up.<br />Competing Interests: Declaration of Competing Interest Alaide Chieffo, MD: Proctorship fees from Amaranth Medical Inc. Juan F. Granada, MD: Scientific advisor and equity shareholder Amaranth Medical Inc. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.<br /> (Copyright © 2020. Published by Elsevier B.V.)
- Subjects :
- Absorbable Implants
Colombia
Coronary Angiography
Humans
Italy
Molecular Weight
Prospective Studies
Prosthesis Design
Sirolimus
Tomography, Optical Coherence
Treatment Outcome
Cardiovascular Agents therapeutic use
Coronary Artery Disease diagnostic imaging
Coronary Artery Disease drug therapy
Coronary Artery Disease surgery
Coronary Restenosis drug therapy
Drug-Eluting Stents
Percutaneous Coronary Intervention
Subjects
Details
- Language :
- English
- ISSN :
- 1874-1754
- Volume :
- 321
- Database :
- MEDLINE
- Journal :
- International journal of cardiology
- Publication Type :
- Academic Journal
- Accession number :
- 32810542
- Full Text :
- https://doi.org/10.1016/j.ijcard.2020.08.014