Title
Antithrombotic Therapy in Patients with Atrial Fibrillation and Acute Coronary Syndrome Treated Medically or with Percutaneous Coronary Intervention or Undergoing Elective Percutaneous Coronary Intervention: Insights from the AUGUSTUS Trial
Date Issued
03 December 2019
Access level
open access
Resource Type
journal article
Author(s)
Windecker S.
Lopes R.D.
Massaro T.
Jones-Burton C.
Granger C.B.
Aronson R.
Heizer G.
Goodman S.G.
Darius H.
Jones W.S.
Aschermann M.
Brieger D.
Cura F.
Engstrøm T.
Fridrich V.
Halvorsen S.
Huber K.
Kang H.J.
Leiva-Pons J.L.
Lewis B.S.
Meneveau N.
Merkely B.
Milicic D.
Morais J.
Potpara T.S.
Raev D.
Sabaté M.
De Waha-Thiele S.
Welsh R.C.
Xavier D.
Mehran R.
Alexander J.H.
Publisher(s)
Lippincott Williams and Wilkins
Abstract
Background: The safety and efficacy of antithrombotic regimens may differ between patients with atrial fibrillation who have acute coronary syndromes (ACS), treated medically or with percutaneous coronary intervention (PCI), and those undergoing elective PCI. Methods: Using a 2×2 factorial design, we compared apixaban with vitamin K antagonists and aspirin with placebo in patients with atrial fibrillation who had ACS or were undergoing PCI and were receiving a P2Y12 inhibitor. We explored bleeding, death and hospitalization, as well as death and ischemic events, by antithrombotic strategy in 3 prespecified subgroups: Patients with ACS treated medically, patients with ACS treated with PCI, and those undergoing elective PCI. Results: Of 4614 patients enrolled, 1097 (23.9%) had ACS treated medically, 1714 (37.3%) had ACS treated with PCI, and 1784 (38.8%) had elective PCI. Apixaban compared with vitamin K antagonist reduced International Society on Thrombosis and Haemostasis major or clinically relevant nonmajor bleeding in patients with ACS treated medically (hazard ratio [HR], 0.44 [95% CI, 0.28-0.68]), patients with ACS treated with PCI (HR, 0.68 [95% CI, 0.52-0.89]), and patients undergoing elective PCI (HR, 0.82 [95% CI, 0.64-1.04]; Pinteraction=0.052) and reduced death or hospitalization in the ACS treated medically (HR, 0.71 [95% CI, 0.54-0.92]), ACS treated with PCI (HR, 0.88 [95% CI, 0.74-1.06]), and elective PCI (HR, 0.87 [95% CI, 0.72-1.04]; Pinteraction=0.345) groups. Compared with vitamin K antagonists, apixaban resulted in a similar effect on death and ischemic events in the ACS treated medically, ACS treated with PCI, and elective PCI groups (Pinteraction=0.356). Aspirin had a higher rate of bleeding than did placebo in patients with ACS treated medically (HR, 1.49 [95% CI, 0.98-2.26]), those with ACS treated with PCI (HR, 2.02 [95% CI, 1.53-2.67]), and those undergoing elective PCI (HR, 1.91 [95% CI, 1.48-2.47]; Pinteraction=0.479). For the same comparison, there was no difference in outcomes among the 3 groups for the composite of death or hospitalization (Pinteraction=0.787) and death and ischemic events (Pinteraction=0.710). Conclusions: An antithrombotic regimen consisting of apixaban and a P2Y12 inhibitor without aspirin provides superior safety and similar efficacy in patients with atrial fibrillation who have ACS, whether managed medically or with PCI, and those undergoing elective PCI compared with regimens that include vitamin K antagonists, aspirin, or both.
Start page
1921
End page
1932
Volume
140
Issue
23
Language
English
OCDE Knowledge area
Sistema cardiaco, Sistema cardiovascular
Subjects
Scopus EID
2-s2.0-85075526111
PubMed ID
Source
Circulation
ISSN of the container
00097322
Sponsor(s)
The AUGUSTUS study was funded by Bristol-Myers Squibb (Princeton, NJ) and Pfizer, Inc (New York, NY). The study was designed and led by an academic steering committee whose members were responsible for the conduct of the trial. The current analyses were designed by the authors, who were responsible for the collection, analysis, and interpretation of the data; writing of the report; and the decision to submit the article for publication. The corresponding author (R.D.L.) had full access to all the data in the study and had final responsibility for the decision to submit for publication.
Sources of information:
Directorio de Producción Científica
Scopus