Relationship of stroke and bleeding risk profiles to efficacy and safety of dabigatran dual therapy versus warfarin triple therapy in atrial fibrillation after percutaneous coronary intervention: An ancillary analysis from the RE-DUAL PCI 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:
06 2019
Historique:
received: 21 10 2018
accepted: 19 02 2019
pubmed: 1 4 2019
medline: 6 2 2020
entrez: 1 4 2019
Statut: ppublish

Résumé

In the RE-DUAL PCI trial of patients with atrial fibrillation (AF) who underwent percutaneous coronary intervention (PCI), dabigatran dual therapy (110 or 150 mg bid, plus clopidogrel or ticagrelor) reduced International Society on Thrombosis and Haemostasis bleeding events compared with warfarin triple therapy, with noninferiority in overall thromboembolic events. This analysis assessed outcomes in relation to patient bleeding and stroke risk profiles, based on the modified HAS-BLED and CHA The primary endpoint, major bleeding event (MBE) or clinically relevant nonmajor bleeding event (CRNMBE), was compared across study arms in patients categorized by modified HAS-BLED score 0-2 or ≥3. The composite endpoint of death, thromboembolic event, and unplanned revascularization rates was compared in patients categorized by CHA Risk of MBE or CRNMBE was lower with dabigatran dual therapy (both doses) versus warfarin triple therapy, irrespective of modified HAS-BLED category (treatment-by-subgroup interaction P-value 0.584 and 0.273 for dabigatran 110 and 150 mg dual therapy, respectively, vs warfarin). Risk of the composite thromboembolic endpoint was similar across CHA Dabigatran dual therapy reduced bleeding events irrespective of bleeding risk category and demonstrated similar efficacy regardless of stroke risk category when compared with warfarin triple therapy.

Sections du résumé

BACKGROUND
In the RE-DUAL PCI trial of patients with atrial fibrillation (AF) who underwent percutaneous coronary intervention (PCI), dabigatran dual therapy (110 or 150 mg bid, plus clopidogrel or ticagrelor) reduced International Society on Thrombosis and Haemostasis bleeding events compared with warfarin triple therapy, with noninferiority in overall thromboembolic events. This analysis assessed outcomes in relation to patient bleeding and stroke risk profiles, based on the modified HAS-BLED and CHA
METHODS
The primary endpoint, major bleeding event (MBE) or clinically relevant nonmajor bleeding event (CRNMBE), was compared across study arms in patients categorized by modified HAS-BLED score 0-2 or ≥3. The composite endpoint of death, thromboembolic event, and unplanned revascularization rates was compared in patients categorized by CHA
RESULTS
Risk of MBE or CRNMBE was lower with dabigatran dual therapy (both doses) versus warfarin triple therapy, irrespective of modified HAS-BLED category (treatment-by-subgroup interaction P-value 0.584 and 0.273 for dabigatran 110 and 150 mg dual therapy, respectively, vs warfarin). Risk of the composite thromboembolic endpoint was similar across CHA
CONCLUSION
Dabigatran dual therapy reduced bleeding events irrespective of bleeding risk category and demonstrated similar efficacy regardless of stroke risk category when compared with warfarin triple therapy.

Identifiants

pubmed: 30928824
pii: S0002-8703(19)30040-7
doi: 10.1016/j.ahj.2019.02.006
pii:
doi:

Substances chimiques

Anticoagulants 0
Warfarin 5Q7ZVV76EI
Clopidogrel A74586SNO7
Ticagrelor GLH0314RVC
Dabigatran I0VM4M70GC

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

13-22

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Gregory Y H Lip (GYH)

Liverpool Centre for Cardiovascular Science, University of Liverpool and Liverpool Heart and Chest Hospital, Liverpool, United Kingdom; Aalborg Thrombosis Research Unit, Department of Clinical Medicine, Aalborg University, Aalborg, Denmark. Electronic address: gregory.lip@liverpool.ac.uk.

Laura Mauri (L)

Brigham and Women's Hospital, Boston, MA.

Gilles Montalescot (G)

Sorbonne University-Paris VI, ACTION Study Group, Pitié-Salpêtrière Hospital, Paris, France.

Mick Ozkor (M)

St Bartholomew's Hospital, London, United Kingdom.

Panagiotis Vardas (P)

Heart Sector, Hygeia Group Hospitals, Athens, Greece.

Philippe Gabriel Steg (PG)

FACT, an F-CRIN Network, DHU FIRE, Université Paris Diderot, INSERM U_1148 and Hôpital Bichat Assistance Publique-Hôpitaux de Paris, Paris, France.

Deepak L Bhatt (DL)

Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School, Boston, MA.

Stefan H Hohnloser (SH)

Johann Wolfgang Goethe University, Department of Cardiology, Division of Clinical Electrophysiology, Frankfurt/Main, Germany.

Corinna Miede (C)

HMS Analytical Software GmbH, Weimar, (Lahn), Germany.

Matias Nordaby (M)

Boehringer Ingelheim International GmbH, Ingelheim, Germany.

Martina Brueckmann (M)

Boehringer Ingelheim International GmbH, Ingelheim, Germany; Faculty of Medicine, University of Heidelberg, Mannheim, Germany.

Joerg Kreuzer (J)

Boehringer Ingelheim Singapore Pte. Ltd, Singapore.

Takeshi Kimura (T)

Kyoto University, Department of Cardiovascular Medicine, Kyoto, Japan.

Jonas Oldgren (J)

Uppsala Clinical Research Center and Department of Medical Sciences, Uppsala University, Uppsala, Sweden.

Jurrien M Ten Berg (JM)

St. Antonius Ziekenhuis, Nieuwegein, The Netherlands.

Christopher P Cannon (CP)

Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School, Boston, MA.

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Classifications MeSH