Effect of Lesion Complexity and Clinical Risk Factors on the Efficacy and Safety of Dabigatran Dual Therapy Versus Warfarin Triple Therapy in Atrial Fibrillation After Percutaneous Coronary Intervention: A Subgroup Analysis From the REDUAL PCI Trial.


Journal

Circulation. Cardiovascular interventions
ISSN: 1941-7632
Titre abrégé: Circ Cardiovasc Interv
Pays: United States
ID NLM: 101499602

Informations de publication

Date de publication:
04 2020
Historique:
entrez: 8 4 2020
pubmed: 8 4 2020
medline: 11 11 2020
Statut: ppublish

Résumé

The REDUAL PCI trial (Evaluation of Dual Therapy With Dabigatran vs Triple Therapy With Warfarin in Patients With AF That Undergo a PCI With Stenting) demonstrated that, in patients with atrial fibrillation following percutaneous coronary intervention, bleeding risk was lower with dabigatran plus clopidogrel or ticagrelor (dual therapy) than warfarin plus clopidogrel or ticagrelor and aspirin (triple therapy). Dual therapy was noninferior for risk of thromboembolic events. Whether these results apply equally to patients at higher risk of ischemic events due to lesion complexity or clinical risk factors is unclear. The primary end point was time to first major or clinically relevant nonmajor bleeding event. The composite efficacy end point was death, thromboembolic event, or unplanned revascularization. Our prespecified subgroup analysis categorized patients by presence of procedural complexity and/or clinical complexity factors at baseline. A modified dual antiplatelet therapy score categorized patients according to degree of clinical risk. Of 2725 patients, 43.1% had clinical complexity factors alone, 9.9% procedural factors alone, 10.0% both, and 37.0% neither. Risk of the primary bleeding end point was lower in both dabigatran dual therapy groups than warfarin triple therapy groups, regardless of procedural and/or clinical lesion complexity (interaction In patients with atrial fibrillation undergoing percutaneous coronary intervention, dabigatran 110 and 150 mg dual therapy reduced bleeding risk compared with warfarin triple therapy, with a similar risk of thromboembolic outcomes, irrespective of procedural and/or clinical complexity and modified dual antiplatelet therapy score. Registration: URL: https://clinicaltrials.gov/; Unique identifier: NCT02164864.

Sections du résumé

BACKGROUND
The REDUAL PCI trial (Evaluation of Dual Therapy With Dabigatran vs Triple Therapy With Warfarin in Patients With AF That Undergo a PCI With Stenting) demonstrated that, in patients with atrial fibrillation following percutaneous coronary intervention, bleeding risk was lower with dabigatran plus clopidogrel or ticagrelor (dual therapy) than warfarin plus clopidogrel or ticagrelor and aspirin (triple therapy). Dual therapy was noninferior for risk of thromboembolic events. Whether these results apply equally to patients at higher risk of ischemic events due to lesion complexity or clinical risk factors is unclear.
METHODS
The primary end point was time to first major or clinically relevant nonmajor bleeding event. The composite efficacy end point was death, thromboembolic event, or unplanned revascularization. Our prespecified subgroup analysis categorized patients by presence of procedural complexity and/or clinical complexity factors at baseline. A modified dual antiplatelet therapy score categorized patients according to degree of clinical risk.
RESULTS
Of 2725 patients, 43.1% had clinical complexity factors alone, 9.9% procedural factors alone, 10.0% both, and 37.0% neither. Risk of the primary bleeding end point was lower in both dabigatran dual therapy groups than warfarin triple therapy groups, regardless of procedural and/or clinical lesion complexity (interaction
CONCLUSIONS
In patients with atrial fibrillation undergoing percutaneous coronary intervention, dabigatran 110 and 150 mg dual therapy reduced bleeding risk compared with warfarin triple therapy, with a similar risk of thromboembolic outcomes, irrespective of procedural and/or clinical complexity and modified dual antiplatelet therapy score. Registration: URL: https://clinicaltrials.gov/; Unique identifier: NCT02164864.

Identifiants

pubmed: 32252548
doi: 10.1161/CIRCINTERVENTIONS.119.008349
doi:

Substances chimiques

Anticoagulants 0
Antithrombins 0
Platelet Aggregation Inhibitors 0
Warfarin 5Q7ZVV76EI
Clopidogrel A74586SNO7
Ticagrelor GLH0314RVC
Dabigatran I0VM4M70GC
Aspirin R16CO5Y76E

Banques de données

ClinicalTrials.gov
['NCT02164864', 'NCT02164864']

Types de publication

Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e008349

Auteurs

Natalia C Berry (NC)

Mid-Atlantic Permanente Medical Group, McLean, VA (N.C.B.).

Laura Mauri (L)

Medtronic, Minneapolis, MN (L.M.).

Philippe Gabriel Steg (PG)

Université de Paris, FACT, INSERM U_1148 and Hôpital Bichat, Assistance Publique-Hôpitaux de Paris, France (P.G.S.).

Deepak L Bhatt (DL)

Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School, Boston, MA (D.L.B., C.P.C.).

Stefan H Hohnloser (SH)

Johann Wolfgang Goethe University, Frankfurt am Main, Germany (S.H.H.).

Matias Nordaby (M)

Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany (M.N.).

Corinna Miede (C)

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

Takeshi Kimura (T)

Kyoto University, Japan (T.K.).

Gregory Y H Lip (GYH)

Liverpool Centre for Cardiovascular Science, University of Liverpool and Liverpool Heart and Chest Hospital, United Kingdom (G.Y.H.L.).
Aalborg Thrombosis Research Unit, Department of Clinical Medicine, Aalborg University, Denmark (G.Y.H.L).

Jonas Oldgren (J)

Uppsala Clinical Research Center and Department of Medical Sciences, Uppsala University, Sweden (J.O.).

Jurriën M Ten Berg (JM)

St Antonius Ziekenhuis, Nieuwegein, the Netherlands (J.M.t.B.).

Christopher P Cannon (CP)

Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School, Boston, MA (D.L.B., C.P.C.).

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Classifications MeSH