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  3. Apixaban and Limiting Aspirin for Patients With Atrial Fibrillation, Percutaneous Coronary Intervention, and Multimorbidity.
 

Apixaban and Limiting Aspirin for Patients With Atrial Fibrillation, Percutaneous Coronary Intervention, and Multimorbidity.

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BORIS DOI
10.48620/78546
Date of Publication
November 2024
Publication Type
Article
Division/Institute

Clinic of Cardiology

Author
Krychtiuk, Konstantin A
Lopes, Renato D
Wojdyla, Daniel M
Goodman, Shaun G
Aronson, Ronald
Windecker, Stephan
Clinic of Cardiology
Mehran, Roxana
Granger, Christopher B
Alexander, John H
Alexander, Karen P
Subject(s)

600 - Technology::610...

Series
JACC: Advances
ISSN or ISBN (if monograph)
2772-963X
Publisher
Elsevier
Language
English
Publisher DOI
10.1016/j.jacadv.2024.101335
PubMed ID
39493312
Uncontrolled Keywords

PCI

anticoagulation

apixaban

aspirin

atrial fibrillation

bleeding

multimorbidity

Description
Background
Patients with atrial fibrillation (AF) after an acute coronary syndrome (ACS) and/or undergoing percutaneous coronary intervention (PCI) with multiple comorbidities are at increased risk for bleeding and ischemic events.Objectives
This post-hoc analysis of AUGUSTUS describes the safety and efficacy of antithrombotic regimens in patients with multimorbidity.Methods
AUGUSTUS was a 2 × 2 factorial, randomized controlled trial evaluating the safety of apixaban vs vitamin K antagonists (VKA) (open-label) and aspirin vs placebo (double-blind) in patients with AF and ACS and/or PCI treated with a P2Y12 inhibitor. Patients were categorized as having no multimorbidity (0-2 comorbidities), moderate multimorbidity (3-4 comorbidities), or high multimorbidity (≥5 comorbidities). The associations between multimorbidity and clinical outcomes and interactions with antithrombotic regimens were tested.Results
Of 4,493 patients (97.4%) with available comorbidity data, 1,897 (42.2%) had no multimorbidity, 2,110 (47%) had moderate, and 486 (10.8%) had high multimorbidity. Patients with moderate (HR: 1.23; 95% CI: 1.02-1.47) and high (HR: 1.98; 95% CI: 1.55-2.54) multimorbidity had higher rates of International Society on Thrombosis and Haemostasis (ISTH) major or clinically relevant nonmajor (CRNM) bleeding compared to patients with no multimorbidity. No significant interaction between multimorbidity and apixaban vs vitamin K antagonists was observed for ISTH major bleeding/CRNM (P int = 0.415), death or hospitalization (P int = 0.092), or death or ischemic event (P int = 0.299). Similarly, no significant interaction between multimorbidity and aspirin vs placebo was seen for ISTH major bleeding/CRNM (P int = 0.261), death or hospitalization (P int = 0.646), or death or ischemic event (P int = 0.608).Conclusions
Our findings support the standard use of apixaban plus a P2Y12 inhibitor in patients with AF and ACS/PCI, irrespective of the presence of multimorbidity.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/189713
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1-s2.0-S2772963X2400615X-main.pdftextAdobe PDF1.15 MBpublishedOpen
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