A randomized, double-blind, placebo-controlled trial investigating the effect of ticagrelor on saphenous vein graft patency in patients undergoing coronary artery bypass grafting surgery-Rationale and design of the POPular CABG 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:
02 2020
Historique:
received: 29 10 2019
accepted: 06 12 2019
pubmed: 31 12 2019
medline: 24 4 2020
entrez: 30 12 2019
Statut: ppublish

Résumé

An estimated 15% of saphenous vein grafts (SVGs) occlude in the first year after coronary artery bypass grafting (CABG) despite aspirin therapy. Graft occlusion can result in symptoms, myocardial infarction, and death. SVG occlusion is primarily caused by atherothrombosis, in which platelet activation plays a pivotal role. Evidence regarding the effect of stronger platelet inhibition on SVG patency after CABG is limited. The main objective of the POPular CABG trial is to determine whether dual antiplatelet therapy with aspirin plus ticagrelor improves SVG patency when compared to aspirin alone. The POPular CABG is a randomized, double-blind, placebo-controlled, multicenter trial investigating the effect of adding ticagrelor to standard aspirin therapy on the rate of SVG occlusion. A total of 500 patients undergoing CABG with ≥ 1 SVG are randomized to ticagrelor or placebo. The primary end point is SVG occlusion rate, assessed with coronary computed tomography angiography at 1 year. Secondary end points are stenoses and occlusions in both SVGs and arterial grafts and SVG failure at 1 year, defined as a composite of SVG occlusion on coronary computed tomography angiography or coronary angiography, SVG revascularization, myocardial infarction in the territory supplied by an SVG, or sudden death. Safety end points are bleeding events at 30 days and 1 year. The POPular CABG trial investigates whether adding ticagrelor to standard aspirin after CABG reduces the rate of SVG occlusion at 1 year.

Identifiants

pubmed: 31884246
pii: S0002-8703(19)30341-2
doi: 10.1016/j.ahj.2019.12.001
pii:
doi:

Substances chimiques

Placebos 0
Platelet Aggregation Inhibitors 0
Ticagrelor GLH0314RVC
Aspirin R16CO5Y76E

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

237-245

Informations de copyright

Copyright © 2019. Published by Elsevier Inc.

Auteurs

Laura M Willemsen (LM)

Department of Cardiology and Cardiothoracic Surgery, St Antonius Hospital, Nieuwegein, the Netherlands.

Paul W A Janssen (PWA)

Department of Cardiology and Cardiothoracic Surgery, St Antonius Hospital, Nieuwegein, the Netherlands.

Chris M Hackeng (CM)

Department of Clinical Chemistry, St Antonius Hospital, Nieuwegein, the Netherlands.

Johannes C Kelder (JC)

Department of Cardiology and Cardiothoracic Surgery, St Antonius Hospital, Nieuwegein, the Netherlands.

Jan G P Tijssen (JGP)

Department of Cardiology, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.

Albert H M van Straten (AHM)

Department of Cardiothoracic Surgery, Catharina Hospital, Eindhoven, the Netherlands.

Mohammed A Soliman-Hamad (MA)

Department of Cardiothoracic Surgery, Catharina Hospital, Eindhoven, the Netherlands.

Vera H M Deneer (VHM)

Department of Clinical Pharmacy, Division of Laboratories, Pharmacy, and Biomedical Genetics, University Medical Center Utrecht, Utrecht.

Edgar J Daeter (EJ)

Department of Cardiology and Cardiothoracic Surgery, St Antonius Hospital, Nieuwegein, the Netherlands.

Uday Sonker (U)

Department of Cardiology and Cardiothoracic Surgery, St Antonius Hospital, Nieuwegein, the Netherlands.

Patrick Klein (P)

Department of Cardiology and Cardiothoracic Surgery, St Antonius Hospital, Nieuwegein, the Netherlands.

Jurriën M Ten Berg (JM)

Department of Cardiology and Cardiothoracic Surgery, St Antonius Hospital, Nieuwegein, the Netherlands. Electronic address: jurtenberg@gmail.com.

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