Comparison among ultra-thin coronary stents: a network meta-analysis.

Network meta-analysis Percutaneous coronary intervention Ultrathin drug-eluting stents

Journal

The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277

Informations de publication

Date de publication:
30 Jan 2024
Historique:
received: 09 10 2023
revised: 08 01 2024
accepted: 19 01 2024
medline: 2 2 2024
pubmed: 2 2 2024
entrez: 1 2 2024
Statut: aheadofprint

Résumé

Ultrathin-strut DES have been related to potential improvement in stent-related outcomes compared to thicker-struts drug-eluting stents (DESs). However, comparisons among different ultrathin devices are lacking. All randomized controlled trials comparing ultrathin (struts thickness < 70 µm) and thicker-struts DESs in an all-comers population were included. Target lesion failure (TLF), as defined by included trials, at 1-year follow-up was the primary endpoint. Overall mortality, myocardial infarction, target lesion revascularization (TLR), and stent thrombosis were the secondary endpoints. Arms of included trials were compared by means of network meta-analysis. Nine studies encompassing 20081 patients were included, of which 9509 patients had an ultrathin DES: Orsiro (evaluated in 7 arms with 8086 patients), MiStent (one arm with 703 patients), or Supraflex (one arm with 720 patients). At 1-year follow-up, no significant differences were noted for TLF among these ultrathin DES. In particular, Orsiro was associated with a similar risk of TLF compared with Supraflex (RR, 1.07; 95% confidence interval, 0.59-1.78) and showed the highest probability of performing best in terms of TLF, myocardial infarction and TLR. Ultrathin DESs are all associated with a comparable risk of TLF as compared with thicker-strut DESs. In terms of TLR and TLF risk, Orsiro was the one with the highest probability of best performances, either compared to other ultrathin DESs or to devices with thicker struts.

Sections du résumé

BACKGROUND BACKGROUND
Ultrathin-strut DES have been related to potential improvement in stent-related outcomes compared to thicker-struts drug-eluting stents (DESs). However, comparisons among different ultrathin devices are lacking.
METHODS METHODS
All randomized controlled trials comparing ultrathin (struts thickness < 70 µm) and thicker-struts DESs in an all-comers population were included. Target lesion failure (TLF), as defined by included trials, at 1-year follow-up was the primary endpoint. Overall mortality, myocardial infarction, target lesion revascularization (TLR), and stent thrombosis were the secondary endpoints. Arms of included trials were compared by means of network meta-analysis.
RESULTS RESULTS
Nine studies encompassing 20081 patients were included, of which 9509 patients had an ultrathin DES: Orsiro (evaluated in 7 arms with 8086 patients), MiStent (one arm with 703 patients), or Supraflex (one arm with 720 patients). At 1-year follow-up, no significant differences were noted for TLF among these ultrathin DES. In particular, Orsiro was associated with a similar risk of TLF compared with Supraflex (RR, 1.07; 95% confidence interval, 0.59-1.78) and showed the highest probability of performing best in terms of TLF, myocardial infarction and TLR.
CONCLUSIONS CONCLUSIONS
Ultrathin DESs are all associated with a comparable risk of TLF as compared with thicker-strut DESs. In terms of TLR and TLF risk, Orsiro was the one with the highest probability of best performances, either compared to other ultrathin DESs or to devices with thicker struts.

Identifiants

pubmed: 38301755
pii: S0002-9149(24)00067-5
doi: 10.1016/j.amjcard.2024.01.018
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: THOMAS PILGRIM reports a relationship with BIOTRONIK Inc that includes: funding grants.

Auteurs

Giorgio Marengo (G)

Division of Cardiology, Cardiovascular and Thoracic Department and Città della Salute e della Scienza, Turin Cardiology, Department of Medical Sciences, University of Turin, Italy.

Francesco Bruno (F)

Division of Cardiology, Cardiovascular and Thoracic Department and Città della Salute e della Scienza, Turin Cardiology, Department of Medical Sciences, University of Turin, Italy. Electronic address: cescobruno@hotmail.it.

Luca Scudeler (L)

Division of Cardiology, Cardiovascular and Thoracic Department and Città della Salute e della Scienza, Turin Cardiology, Department of Medical Sciences, University of Turin, Italy.

Federica Savoca (F)

Division of Cardiology, Cardiovascular and Thoracic Department and Città della Salute e della Scienza, Turin Cardiology, Department of Medical Sciences, University of Turin, Italy.

Daniela Zugna (D)

Cancer Epidemiology Unit, Department of Medical Sciences, University of Turin, Turin, Italy.

Elena Isaevska (E)

Cancer Epidemiology Unit, Department of Medical Sciences, University of Turin, Turin, Italy.

Thomas Pilgrim (T)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, CH-3010, Bern, Switzerland.

Lisette Okkels Jensen (LO)

Odense University Hospital, Odense, Denmark.

Ovidio De Filippo (O)

Division of Cardiology, Cardiovascular and Thoracic Department and Città della Salute e della Scienza, Turin Cardiology, Department of Medical Sciences, University of Turin, Italy.

Lorenzo Richiardi (L)

Cancer Epidemiology Unit, Department of Medical Sciences, University of Turin, Turin, Italy.

Gaetano Maria De Ferrari (GM)

Division of Cardiology, Cardiovascular and Thoracic Department and Città della Salute e della Scienza, Turin Cardiology, Department of Medical Sciences, University of Turin, Italy.

Fabrizio D'Ascenzo (F)

Division of Cardiology, Cardiovascular and Thoracic Department and Città della Salute e della Scienza, Turin Cardiology, Department of Medical Sciences, University of Turin, Italy.

Classifications MeSH