Opportunities for enhancing the care of older patients with ST-elevation myocardial infarction presenting for primary percutaneous coronary intervention: Rationale and design of the SAFE-STEMI for Seniors trial.


Journal

American heart journal
ISSN: 1097-6744
Titre abrégé: Am Heart J
Pays: United States
ID NLM: 0370465

Informations de publication

Date de publication:
12 2019
Historique:
received: 25 06 2019
accepted: 18 09 2019
pubmed: 13 11 2019
medline: 13 3 2020
entrez: 13 11 2019
Statut: ppublish

Résumé

Advanced age is directly related to worse outcomes following ST-elevation myocardial infarction (STEMI) and higher complication rates from antithrombotic therapies and primary percutaneous coronary intervention (PCI). Often excluded from clinical trials, seniors presenting with STEMI remain an understudied population despite contributing to 140,000 hospital admissions annually. The SAFE-STEMI for Seniors study is a prospective, multicenter, unblinded, randomized clinical trial designed to examine the efficacy and safety of instantaneous wave-free ratio-guided complete revascularization in multivessel disease, while also investigating other components of STEMI care for patients ≥60 years including the efficacy and safety of zotarolimus-eluting stents for primary PCI and transradial PCI with the Glidesheath Slender and TR band. The SAFE-STEMI trial represents North America's first and only prospective randomized investigational device exemption study to use a Coordinated Registry Network infrastructure with collaborative partnering across industry manufacturers, promoting both efficiency and reduced cost of evidence development for regulatory decisions related to both diagnostic and therapeutic technologies in a single study design. The study has been powered to evaluate 2 independent co-primary end points in a population of older patients with STEMI: (1) third-generation drug-eluting stents for primary PCI and (2) instantaneous wave-free ratio-guided complete revascularization versus infarct-related artery-only revascularization.

Identifiants

pubmed: 31715434
pii: S0002-8703(19)30272-8
doi: 10.1016/j.ahj.2019.09.014
pii:
doi:

Substances chimiques

Immunosuppressive Agents 0
zotarolimus H4GXR80IZE
Sirolimus W36ZG6FT64

Types de publication

Clinical Trial Protocol Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

84-91

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Jennifer A Rymer (JA)

From the Department of Medicine, Division of Cardiology, Duke University Medical Center, Durham, NC; Duke Clinical Research Institute, Durham, NC. Electronic address: jennifer.rymer@duke.edu.

Aditya Mandawat (A)

From the Department of Medicine, Division of Cardiology, Duke University Medical Center, Durham, NC.

J Dawn Abbott (JD)

Lifespan Cardiovascular Institute, Providence, RI.

Mauricio G Cohen (MG)

University of Miami Health System, Miami, FL.

Justin E Davies (JE)

Imperial College Division of Cardiology, London, UK.

Ian C Gilchrist (IC)

Penn State Heart and Vascular Institute, Hershey, PA.

Sanjit S Jolly (SS)

Population Health Research Institute, McMaster University, Hamilton General Hospital, Hamilton, Ontario, Canada.

Jeffrey J Popma (JJ)

Beth Beth Israel Deaconess Medical Center, Boston, MA.

Hussein R Al-Khalidi (HR)

Duke Clinical Research Institute, Durham, NC.

Sunil V Rao (SV)

From the Department of Medicine, Division of Cardiology, Duke University Medical Center, Durham, NC; Duke Clinical Research Institute, Durham, NC.

David Kong (D)

From the Department of Medicine, Division of Cardiology, Duke University Medical Center, Durham, NC; Duke Clinical Research Institute, Durham, NC.

Mitchell Krucoff (M)

From the Department of Medicine, Division of Cardiology, Duke University Medical Center, Durham, NC; Duke Clinical Research Institute, Durham, NC.

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