Safety and Efficacy of Double Antithrombotic Therapy With Non-Vitamin K Antagonist Oral Anticoagulants in Patients With Atrial Fibrillation Undergoing Percutaneous Coronary Intervention: A Systematic Review and Meta-Analysis.

Davide Capodanno, Marco Di Maio, Antonio Greco, Deepak L Bhatt, C Michael Gibson, Andreas Goette, Renato D Lopes, Roxana Mehran, Pascal Vranckx, Dominick J Angiolillo

Journal: Journal of the American Heart Association 2021;9(16):e017212

PMID: 32805186

Abstract

Background The optimal antithrombotic therapy for patients with atrial fibrillation undergoing percutaneous coronary intervention is a topic of debate. We aimed at defining the efficacy and safety of double antithrombotic therapy with single antiplatelet therapy (SAPT) plus a non-vitamin K antagonist oral anticoagulant (NOAC) against triple antithrombotic therapy with dual antiplatelet therapy (DAPT) added to a vitamin K antagonist (VKA), illustrating the pooled cumulative distribution of events, the ranking of different NOACs tested in NOAC+SAPT combination strategies, and the state of the current evidence in the field. Methods and Results Randomized controlled trials meeting the inclusion criteria were identified. The primary efficacy end point was the composite of trial-defined major adverse cardiac events. The primary safety end point was clinically significant bleeding. Secondary end points were the components of primary end points. Trial-level pairwise and Bayesian network meta-analyses, reconstructed Kaplan-Meier analyses, and trial sequential analysis were performed. Four randomized controlled trials (10 969 patients) were included. No differences were found in terms of major adverse cardiac events (hazard ratio [HR], 1.07; 95% CI, 0.94-1.22), and the NOAC+SAPT strategy showed a lower rate of clinically significant bleeding compared with VKA + DAPT (HR, 0.56; 95% CI, 0.39-0.80). These results were consistent in reconstructed Kaplan-Meier analyses. In the Bayesian network meta-analysis, different NOACs displayed diverse risk-benefit profiles. Trial sequential analyses suggest that the evidence for the similarity in major adverse cardiac events compared with VKA + DAPT and the bleeding risk reduction observed with NOAC+SAPT is likely to be conclusive. Conclusions NOAC+SAPT does not increase the risk of major adverse cardiac events and reduces the risk of bleeding compared with VKA + DAPT in AF patients undergoing percutaneous coronary intervention. Various NOACs may have different risk-benefit profiles in combination strategies. Registration URL: https://www.crd.york.ac.uk/prospero/; Unique identifier: CRD42020151089.

Address: Division of Cardiology A.O.U. Policlinico "G. Rodolico - S. Marco"University of Catania Italy.; Division of Cardiology A.O.U. Policlinico "G. Rodolico - S. Marco"University of Catania Italy.; Division of Cardiology Department of Translational Medical Sciences University of Campania "Luigi Vanvitelli" Naples Italy.; Department of Medicine Brigham and Women's Hospital and Harvard Medical School Boston MA.; Cardiovascular Division Department of Medicine Beth Israel Deaconess Medical CenterHarvard Medical School Boston MA.; Atrial Fibrillation Network Munster Germany.; Cardiology and Intensive Care Medicine St Vincenz-Hospital Paderborn Germany.; Working Group of Molecular Electrophysiology University Hospital Magdeburg Magdeburg Germany.; Duke Health Duke Clinical Research Institute Durham NC.; Cardiovascular Institute Mount Sinai Medical CenterIcahn School of Medicine at Mount Sinai New York NY.; Jessa Ziekenhuis Faculty of Medicine and Life Sciences at the Hasselt University Hasselt Belgium.; Division of Cardiology University of Florida College of Medicine Jacksonville FL.
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