Percutaneous coronary interventions with the Absorb Bioresorbable vascular scaffold in real life: 1-year results from the FRANCE ABSORB registry.


Journal

Archives of cardiovascular diseases
ISSN: 1875-2128
Titre abrégé: Arch Cardiovasc Dis
Pays: Netherlands
ID NLM: 101465655

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 03 05 2018
revised: 13 07 2018
accepted: 06 09 2018
pubmed: 12 1 2019
medline: 23 4 2019
entrez: 12 1 2019
Statut: ppublish

Résumé

Several randomized studies have shown that bioresorbable vascular scaffold (BVS) technology is associated with an increased risk of stent thrombosis. This study aimed to assess the rates of adverse outcomes at 1 year in patients treated with the Absorb BVS (Abbott Vascular, Santa Clara, CA, USA), using data from a large nationwide prospective multicentre registry (FRANCE ABSORB). All patients receiving the Absorb BVS in France were included prospectively in the study. Predilatation, optimal sizing and postdilatation were recommended systematically. The primary endpoint was a composite of cardiovascular death, myocardial infarction and target lesion revascularization at 1 year. Secondary endpoints were scaffold thrombosis and target vessel revascularization at 1 year. A total of 2072 patients at 86 centres were included: mean age 55±11 years; 80% men. The indication was acute coronary syndrome (ACS) in 49% of cases. Predilatation and postdilatation were done in 93% and 83% of lesions, respectively. At 1 year, the primary endpoint occurred in 3.9% of patients, the rate of scaffold thrombosis was 1.5% and the rate of target vessel revascularization was 3.3%. In a multivariable analysis, diabetes and total Absorb BVS length>30mm were independently associated with the occurrence of the primary endpoint, whereas oral anticoagulation and total Absorb BVS length>30mm were independently associated with occurrence of scaffold thrombosis. The Absorb BVS was implanted in a relatively young population, half of whom had ACS. Predilatation and postdilatation rates were high, and 1-year outcomes were acceptable.

Sections du résumé

BACKGROUND BACKGROUND
Several randomized studies have shown that bioresorbable vascular scaffold (BVS) technology is associated with an increased risk of stent thrombosis.
AIM OBJECTIVE
This study aimed to assess the rates of adverse outcomes at 1 year in patients treated with the Absorb BVS (Abbott Vascular, Santa Clara, CA, USA), using data from a large nationwide prospective multicentre registry (FRANCE ABSORB).
METHODS METHODS
All patients receiving the Absorb BVS in France were included prospectively in the study. Predilatation, optimal sizing and postdilatation were recommended systematically. The primary endpoint was a composite of cardiovascular death, myocardial infarction and target lesion revascularization at 1 year. Secondary endpoints were scaffold thrombosis and target vessel revascularization at 1 year.
RESULTS RESULTS
A total of 2072 patients at 86 centres were included: mean age 55±11 years; 80% men. The indication was acute coronary syndrome (ACS) in 49% of cases. Predilatation and postdilatation were done in 93% and 83% of lesions, respectively. At 1 year, the primary endpoint occurred in 3.9% of patients, the rate of scaffold thrombosis was 1.5% and the rate of target vessel revascularization was 3.3%. In a multivariable analysis, diabetes and total Absorb BVS length>30mm were independently associated with the occurrence of the primary endpoint, whereas oral anticoagulation and total Absorb BVS length>30mm were independently associated with occurrence of scaffold thrombosis.
CONCLUSIONS CONCLUSIONS
The Absorb BVS was implanted in a relatively young population, half of whom had ACS. Predilatation and postdilatation rates were high, and 1-year outcomes were acceptable.

Identifiants

pubmed: 30630761
pii: S1875-2136(18)30191-8
doi: 10.1016/j.acvd.2018.09.007
pii:
doi:

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

113-123

Informations de copyright

Copyright © 2018 Elsevier Masson SAS. All rights reserved.

Auteurs

Guillaume Cayla (G)

Service de cardiologie, hôpital universitaire Carémeau, université de Montpellier, CHU de Nîmes, place du Professeur-Robert-Debré, 30029 Nîmes, France. Electronic address: cayla.guillaume@gmail.com.

René Koning (R)

Clinique Saint-Hilaire, 76000 Rouen, France.

Jean Fajadet (J)

Clinique Pasteur, 31076 Toulouse, France.

Joel Sainsous (J)

Clinique Rhône-Durance, 84000 Avignon, France.

Didier Carrié (D)

Hôpital Rangueuil, CHU de Toulouse, 31400 Toulouse, France.

Simon Elhadad (S)

Centre hospitalier de Marne-la-Vallée, 77600 Jossigny, France.

Francois Tarragano (F)

Hôpital Américain, 92200 Neuilly-sur-Seine, France.

Thierry Lefévre (T)

Hôpital privé Jacques-Cartier, Institut Cardiovasculaire Paris-Sud, Ramsay-Générale de Santé, 91300 Massy, France.

Sylvain Ranc (S)

Centre hospitalier Saint-Joseph et Saint-Luc, 69007 Lyon, France.

Said Ghostine (S)

Centre chirurgical Marie-Lannelongue, 92350 Le Plessis Robinson, France.

Philippe Garot (P)

Hôpital privé Claude-Galien, Institut Cardiovasculaire Paris-Sud, Ramsay-Générale de Santé, 91480 Quincy, France.

Frédéric Marco (F)

Polyclinique du Parc, 31400 Toulouse, France.

Luc Maillard (L)

GCS-ES Axium-Rambot, clinique Axium, 13100 Aix-en-Provence, France.

Pascal Motreff (P)

CHU Gabriel-Montpied, 63000 Clermont-Ferrand, France.

Hervé Le Breton (H)

Service de cardiologie et maladies vasculaires, CIC-IT 804, hôpital Pontchaillou, CHU de Rennes, 35033 Rennes, France; Inserm U1099, laboratoire de traitement du signal et de l'image, université de Rennes 1, 35000 Rennes, France.

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