Five-Year Clinical Outcomes of the COBRA Polyzene F NanoCoated Coronary Stent System.


Journal

Cardiovascular revascularization medicine : including molecular interventions
ISSN: 1878-0938
Titre abrégé: Cardiovasc Revasc Med
Pays: United States
ID NLM: 101238551

Informations de publication

Date de publication:
08 2022
Historique:
received: 09 09 2021
revised: 28 11 2021
accepted: 27 12 2021
pubmed: 21 1 2022
medline: 20 7 2022
entrez: 20 1 2022
Statut: ppublish

Résumé

The COBRA Polyzene F™ NanoCoated Coronary Stent System (PzF coated stent) stent demonstrated favorable clinical outcomes at 9 months but late results have not been reported. We sought to assess the late safety and effectiveness of the PzF coated stent for treatment of de novo coronary artery lesions. Patients with de novo coronary artery lesions meeting eligibility criteria were enrolled in a non-randomized, prospective clinical trial and followed for 5 years. The primary endpoint was target vessel failure (TVF, cardiac death, myocardial infarction [MI], or clinically-driven target vessel revascularization [TVR]) at 9 months. Secondary endpoints included major adverse clinical events (MACE, cardiac death, MI, or clinically driven TLR), clinically driven target lesion revascularization (TLR) and definite or probable stent thrombosis during 5-year follow-up. Endpoints at 5 years were analyzed as cumulative incidence accounting for competing risk of death. Of 296 enrolled patients, 290 (98%) were evaluable at 5 years. By 5 years, MACE had occurred in 61 (21.3%), cardiac death in 11 (4.2%), MI in 25 (8.6%), and TLR in 34 (12.0%) subjects. Between follow-up years 1 and 5, a first MACE occurred in 17 (6.2%), including 10 (4.0%) cardiac death, 4 (1.6%) MI, and 7 (2.9%) TLR events. There were no definite or probable stent thromboses. The PzF coated stent demonstrated continued safety and effectiveness through 5 years with low to very low incident rates of MACE, MI, TLR and stent thrombosis between 1 and 5 years after stent placement.

Sections du résumé

BACKGROUND/PURPOSE
The COBRA Polyzene F™ NanoCoated Coronary Stent System (PzF coated stent) stent demonstrated favorable clinical outcomes at 9 months but late results have not been reported. We sought to assess the late safety and effectiveness of the PzF coated stent for treatment of de novo coronary artery lesions.
METHODS
Patients with de novo coronary artery lesions meeting eligibility criteria were enrolled in a non-randomized, prospective clinical trial and followed for 5 years. The primary endpoint was target vessel failure (TVF, cardiac death, myocardial infarction [MI], or clinically-driven target vessel revascularization [TVR]) at 9 months. Secondary endpoints included major adverse clinical events (MACE, cardiac death, MI, or clinically driven TLR), clinically driven target lesion revascularization (TLR) and definite or probable stent thrombosis during 5-year follow-up. Endpoints at 5 years were analyzed as cumulative incidence accounting for competing risk of death.
RESULTS
Of 296 enrolled patients, 290 (98%) were evaluable at 5 years. By 5 years, MACE had occurred in 61 (21.3%), cardiac death in 11 (4.2%), MI in 25 (8.6%), and TLR in 34 (12.0%) subjects. Between follow-up years 1 and 5, a first MACE occurred in 17 (6.2%), including 10 (4.0%) cardiac death, 4 (1.6%) MI, and 7 (2.9%) TLR events. There were no definite or probable stent thromboses.
CONCLUSIONS
The PzF coated stent demonstrated continued safety and effectiveness through 5 years with low to very low incident rates of MACE, MI, TLR and stent thrombosis between 1 and 5 years after stent placement.

Identifiants

pubmed: 35045942
pii: S1553-8389(21)00831-9
doi: 10.1016/j.carrev.2021.12.030
pii:
doi:

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

76-80

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest Drs. Cutlip, Jauhar, Meraj, Garratt, Maillard, Erglis, and Silber report receiving institutional research funding from Celonova. Dr. Victor and Dr. Lena Novack report statistical consulting fees from Ceonova. Dr. Stoler reports receiving institutional research funding from Celonova and serves as a member of the Advisory Board or as a proctor for Medtronic, Boston Scientific, Edwards Lifesciences, and Biotronik. Dr. Barakat is a paid employee of Celonova.

Auteurs

Donald E Cutlip (DE)

Cardiology Division, Beth Israel Deaconess Medical Center, Baim Institute for Clinical Research and Harvard Medical School, Boston, MA, United States of America. Electronic address: dcutlip@bidmc.harvard.edu.

Rajiv Jauhar (R)

North Shore University Hospital, Manhasset, NY, United States of America.

Perwaiz Meraj (P)

North Shore University Hospital, Manhasset, NY, United States of America.

Kirk N Garratt (KN)

ChristianaCare, Wilmington, DE, United States of America.

Victor Novack (V)

Clinical Research Center, Soroka University Medical Center, Beersheba, Israel.

Lena Novack (L)

Clinical Research Center, Soroka University Medical Center, Beersheba, Israel.

Luc Maillard (L)

GCS ES Axium Rambot, Aix-en-Provence, France.

Andrejs Erglis (A)

University of Latvia, Riga, Latvia.

Robert Stoler (R)

Baylor Heart and Vascular Hospital at Baylor University Medical Center, Dallas, TX, United States of America.

Mark Barakat (M)

CeloNova BioSciences, San Antonio, TX, United States of America.

Sigmund Silber (S)

Department of Cardiology, Heart Center at the Isar, Munich, Germany.

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