Safety and efficacy of the COMBO bio-engineered stent in an all-comer PCI cohort: 1-Year final clinical outcomes from the MASCOT post-marketing registry
Language English Country Netherlands Media print-electronic
Document type Journal Article, Multicenter Study, Observational Study
PubMed
30826192
DOI
10.1016/j.ijcard.2019.01.053
PII: S0167-5273(18)31841-2
Knihovny.cz E-resources
- Keywords
- COMBO drug eluting stent, Dual therapy stent, Percutaneous coronary intervention, Target lesion failure,
- MeSH
- Bioengineering methods MeSH
- Time Factors MeSH
- Immunosuppressive Agents pharmacology MeSH
- Percutaneous Coronary Intervention methods MeSH
- Middle Aged MeSH
- Humans MeSH
- Follow-Up Studies MeSH
- Coronary Artery Disease surgery MeSH
- Product Surveillance, Postmarketing statistics & numerical data MeSH
- Prosthesis Design MeSH
- Registries * MeSH
- Retrospective Studies MeSH
- Sirolimus pharmacology MeSH
- Drug-Eluting Stents * MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Observational Study MeSH
- Names of Substances
- Immunosuppressive Agents MeSH
- Sirolimus MeSH
BACKGROUND: The COMBO stent (OrbusNeich Medical, Ft. Lauderdale, Florida) is a new-generation bio-engineered drug eluting stent, combining an abluminal coating of a bioabsorbable polymer matrix for sustained release of sirolimus and luminal anti-CD34 coating for endothelial progenitor cell capture and rapid endothelialization. METHODS: The Multinational Abluminal Sirolimus Coated BiO-Engineered StenT (MASCOT) registry was a prospective post-marketing study conducted from June 2014-May 2017 across 60 centers globally. Patients were eligible if COMBO stent implantation was attempted, and they received dual antiplatelet therapy (DAPT) per local guidelines. Follow-up was conducted by trained research staff at 1, 6 and 12 months by phone or clinic visit to capture clinical events and DAPT cessation events. The primary endpoint was 1-year target lesion failure (TLF), composite of cardiac death, non-fatal myocardial infarction not clearly attributable to a non-target vessel, or ischemia-driven target lesion revascularization. RESULTS: A total of 2614 patients were enrolled over the study period with 96.7% completion of 1-year follow-up. The mean age of enrolled patients was 62.9 ± 11.2 years and 23.0% were female. Diabetes mellitus was present at baseline in 33.5%. A total of 56.1% patients underwent PCI for acute coronary syndrome (ACS). The 1-year primary endpoint of TLF occurred in 3.4% patients (n = 88). Definite stent thrombosis occurred in 0.5% patients (n = 12). CONCLUSION: The MASCOT post marketing registry provides comprehensive safety and efficacy outcomes following contemporary PCI using the novel COMBO stent in an all-comer population. This platform is associated with low rates of 1-year TLF and ST. CLINICALTRIALS. GOV IDENTIFIER: NCT02183454.
2nd Faculty of Medicine and Motol University Hospital Praha Czech Republic
Amphia Hospital Breda Breda Netherlands
Icahn School of Medicine at Mount Sinai New York NY USA
MBAL Puls Blagoevgrad Blagoevgrad Bulgaria
MBAL St Ivan Rilski Stara Zagora Bulgaria
Meixoeiro Hospital University Hospital of Vigo Vigo Spain
Nemocnice na Homolce Praha 5 Czech Republic
OrbusNeich Ltd Fort Lauderdale FL USA
Pusat Jantung Hospital Umum Sarawak Sarawak Malaysia
Queen Elizabeth Hospital Singapore
San Raffaele Scientific Institute Milan Italy
References provided by Crossref.org
ClinicalTrials.gov
NCT02183454