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  3. 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.
 

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.

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BORIS DOI
10.7892/boris.139074
Publisher DOI
10.1161/CIRCULATIONAHA.119.043308
PubMed ID
31557056
Description
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.

CLINICAL TRIAL REGISTRATION

URL: https://www.clinicaltrials.gov. Unique identifier: NCT02415400.
Date of Publication
2019-12-03
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Keyword(s)
acute coronary syndrome anticoagulants antithrombotic therapy aspirin atrial fibrillation hemorrhage percutaneous coronary intervention stroke
Language(s)
en
Contributor(s)
Windecker, Stephan
Universitätsklinik für Kardiologie
Lopes, Renato D
Massaro, Tyler
Jones-Burton, Charlotte
Granger, Christopher B
Aronson, Ronald
Heizer, Gretchen
Goodman, Shaun G
Darius, Harald
Jones, W Schuyler
Aschermann, Michael
Brieger, David
Cura, Fernando
Engstrøm, Thomas
Fridrich, Viliam
Halvorsen, Sigrun
Huber, Kurt
Kang, Hyun-Jae
Leiva-Pons, Jose L
Lewis, Basil S
Malaga, German
Meneveau, Nicolas
Merkely, Bela
Milicic, Davor
Morais, João
Potpara, Tatjana S
Raev, Dimitar
Sabaté, Manel
de Waha-Thiele, Suzanne
Welsh, Robert C
Xavier, Denis
Mehran, Roxana
Alexander, John H
Additional Credits
Universitätsklinik für Kardiologie
Series
Circulation
Publisher
American Heart Association
ISSN
1524-4539
Access(Rights)
restricted
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