Safety and efficacy of double vs. triple antithrombotic therapy in patients with atrial fibrillation with or without acute coronary syndrome undergoing percutaneous coronary intervention: a collaborative meta-analysis of non-vitamin K antagonist oral anticoagulant-based randomized clinical trials.


Journal

European heart journal. Cardiovascular pharmacotherapy
ISSN: 2055-6845
Titre abrégé: Eur Heart J Cardiovasc Pharmacother
Pays: England
ID NLM: 101669491

Informations de publication

Date de publication:
09 04 2021
Historique:
received: 20 08 2020
revised: 10 09 2020
accepted: 23 09 2020
pubmed: 30 10 2020
medline: 31 3 2022
entrez: 29 10 2020
Statut: ppublish

Résumé

Safety and efficacy of antithrombotic regimens in patients with atrial fibrillation (AF) undergoing percutaneous coronary intervention (PCI) may differ based on clinical presentation. We sought to compare double vs. triple antithrombotic therapy (DAT vs. TAT) in AF patients with or without acute coronary syndrome (ACS) undergoing PCI. A systematic review and meta-analysis was performed using PubMed to search for non-vitamin K antagonist oral anticoagulant (NOAC)-based randomized clinical trials. Data on subgroups of ACS or elective PCI were obtained by published reports or trial investigators. A total of 10 193 patients from four NOAC trials were analysed, of whom 5675 presenting with ACS (DAT = 3063 vs. TAT = 2612) and 4518 with stable coronary artery disease (SCAD; DAT = 2421 vs. TAT = 2097). The primary safety endpoint of ISTH major bleeding or clinically relevant non-major bleeding was reduced with DAT compared with TAT in both ACS (12.2% vs. 19.4%; RR 0.63, 95% CI 0.56-0.71; P < 0.0001; I2 = 0%) and SCAD (14.6% vs. 22.0%; RR 0.68, 95% CI 0.55-0.85; P = 0.0008; I2 = 66%), without interaction (P-int = 0.54). Findings were consistent for secondary bleeding endpoints, including intra-cranial haemorrhage. In both subgroups, there was no difference between DAT and TAT for all-cause death, major adverse cardiovascular events, or stroke. Myocardial infarction and stent thrombosis were numerically higher with DAT vs. TAT consistently in ACS and SCAD (P-int = 0.60 and 0.86, respectively). Findings were confirmed by multiple sensitivity analyses, including a separate analysis on dabigatran regimens and a restriction to PCI population. DAT, compared with TAT, is associated with lower bleeding risks, including intra-cranial haemorrhage, and a small non-significant excess of cardiac ischaemic events in both patients with or without ACS.

Identifiants

pubmed: 33119069
pii: 5942977
doi: 10.1093/ehjcvp/pvaa116
pmc: PMC8117456
doi:

Substances chimiques

Anticoagulants 0
Fibrinolytic Agents 0
Platelet Aggregation Inhibitors 0

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

f50-f60

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the European Society of Cardiology.

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Auteurs

Giuseppe Gargiulo (G)

Department of Advanced Biomedical Sciences, Federico II University of Naples, Naples, Italy.

Christopher P Cannon (CP)

Cardiovascular Division, Brigham and Women's Hospital, Heart and Vascular Center and Harvard Medical School, 75 Francis Street, Boston, MA 02115, USA.
Baim Institute for Clinical Research, 930-W Commonwealth Avenue, Boston, MA 02215, USA.

Charles Michael Gibson (CM)

Division of Cardiovascular Medicine, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.

Andreas Goette (A)

St. Vincenz-Hospital, Am Busdorf 2, 33098 Paderborn, Germany.
Working Group of Molecular Electrophysiology, University Hospital Magdeburg, Leipziger Str. 44, 39120 Magdeburg, Germany.
Atrial Fibrillation Network (AFNET), Mendel Str.11, 48149 Münster, Germany.

Renato D Lopes (RD)

Duke Clinical Research Institute, Duke University School of Medicine, 200 Morris Street, Durham, NC 27701, USA.

Jonas Oldgren (J)

Uppsala Clinical Research Center and, Department of Medical Sciences, Uppsala University, Dag Hammarskjolds vag 38, SE-751 85 Uppsala, Sweden.

Serge Korjian (S)

Division of Cardiovascular Medicine, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.

Stephan Windecker (S)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Freiburgstrasse 10, 3030 Bern, Switzerland.

Giovanni Esposito (G)

Department of Advanced Biomedical Sciences, Federico II University of Naples, Naples, Italy.

Pascal Vranckx (P)

Department of Cardiology and Intensive Care Medicine, Jessa Ziekenhuis, Faculty of Medicine and Life Sciences, Hasselt University, Stadsomvaart 11, 3500 Hasselt, Belgium.

Marco Valgimigli (M)

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Freiburgstrasse 10, 3030 Bern, Switzerland.

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