TY - JOUR
T1 - Treatment of atrial fibrillation with concomitant coronary or peripheral artery disease
T2 - Results from the outcomes registry for better informed treatment of atrial fibrillation II
AU - ORBIT AF Patients and Investigators
AU - Inohara, Taku
AU - Shrader, Peter
AU - Pieper, Karen
AU - Blanco, Rosalia G.
AU - Allen, Larry A.
AU - Fonarow, Gregg C.
AU - Gersh, Bernard J.
AU - Go, Alan S.
AU - Ezekowitz, Michael D.
AU - Kowey, Peter R.
AU - Reiffel, James A.
AU - Naccarelli, Gerald V.
AU - Chan, Paul S.
AU - Mahaffey, Kenneth W.
AU - Singer, Daniel E.
AU - Freeman, James V.
AU - Steinberg, Benjamin A.
AU - Peterson, Eric D.
AU - Piccini, Jonathan P.
N1 - Funding Information:
This project was supported in part by cooperative agreement 1 U19 HS021092 from the Agency of Healthcare Research and Quality, and JSPS Overseas Research Fellowship. The Outcomes Registry for Better Informed Treatment of Atrial Fibrillation is sponsored by Janssen Scientific Affairs LLC. With the exception of Janssen Scientific Affairs LLC, the funders had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
Funding Information:
JA Reiffel : Research grant from Janssen Pharmaceuticals. Research support from Boehringer Ingelheim Pharmaceuticals Inc. and GlaxoSmithKline. Consultancies with Sanofi, Gilead Sciences Inc., CV Therapeutics, GlaxoSmithKline, Merck & Co Inc., Cardiome Pharma Corp, Boehringer Ingelheim Pharmaceuticals Inc., and Medtronic Inc. Speakers' bureau income from Sanofi and Boehringer Ingelheim Pharmaceuticals Inc.
Funding Information:
ED Peterson : Research grant from Janssen Pharmaceuticals and Eli Lilly. Consultant for Janssen Pharmaceuticals and Boehringer Ingelheim.
Funding Information:
T Inohara : Research Grant: JSPS Overseas Research fellowship, and Boston Scientific.
Funding Information:
GV Naccarelli : Research Grant from Janssen. Consultant/Advisory Board for Janssen and Daiichi Sankyo.
Funding Information:
BA Steinberg : Research support from Boston Scientific and Janssen. Consult for Janssen. Speakers' bureau income Biosense Webster.
Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2019/7
Y1 - 2019/7
N2 - Background: Treatment patterns and outcomes of individuals with vascular disease who have new-onset atrial fibrillation (AF) are not well characterized. Methods: Among patients with new-onset AF, we analyzed treatment and outcomes in those with or without vascular disease in the ORBIT-AF II registry. Vascular disease was defined as coronary disease with or without myocardial infarction (MI) or revascularization, or peripheral artery disease. The primary outcomes included major adverse cardiovascular or neurological events (MACNE) and major bleeding. Cox proportional hazard models were used to adjust the difference in patient characteristics. Results: Overall 1920 of 6203 (31.0%) of new-onset AF had vascular disease. In patients with vascular disease, 62.2% of those were treated with direct oral anticoagulants (DOACs) and 23.4% with warfarin. Dual therapy and triple therapy were used in 36.9% and 4.9%, respectively. Vascular disease patients had increased risk of MACNE (adjusted hazard ratio [aHR] 1.83 [95%CIs 1.32–2.55]), but not major bleeding (aHR 1.24 [0.95–1.63]). Among patients with vascular disease, relative to those on warfarin, those treated with DOACs had similar risk for MACNE (aHR 1.20 [0.77–1.87]) but lower risks for bleeding, although it did not reach statistical significance (aHR 0.70 [0.43–1.15]). Concomitant antiplatelet therapy was associated with higher bleeding (aHR 2.27 [1.38–3.73]) with no apparent reduction in MACNE (aHR 1.50 [1.00–2.25]). Conclusions: Most patients with AF and vascular disease were managed with oral anticoagulation. About half of them were also treated with concomitant antiplatelet therapy, which was associated with increased risk of bleeding, without evidence of improved cardiovascular outcomes.
AB - Background: Treatment patterns and outcomes of individuals with vascular disease who have new-onset atrial fibrillation (AF) are not well characterized. Methods: Among patients with new-onset AF, we analyzed treatment and outcomes in those with or without vascular disease in the ORBIT-AF II registry. Vascular disease was defined as coronary disease with or without myocardial infarction (MI) or revascularization, or peripheral artery disease. The primary outcomes included major adverse cardiovascular or neurological events (MACNE) and major bleeding. Cox proportional hazard models were used to adjust the difference in patient characteristics. Results: Overall 1920 of 6203 (31.0%) of new-onset AF had vascular disease. In patients with vascular disease, 62.2% of those were treated with direct oral anticoagulants (DOACs) and 23.4% with warfarin. Dual therapy and triple therapy were used in 36.9% and 4.9%, respectively. Vascular disease patients had increased risk of MACNE (adjusted hazard ratio [aHR] 1.83 [95%CIs 1.32–2.55]), but not major bleeding (aHR 1.24 [0.95–1.63]). Among patients with vascular disease, relative to those on warfarin, those treated with DOACs had similar risk for MACNE (aHR 1.20 [0.77–1.87]) but lower risks for bleeding, although it did not reach statistical significance (aHR 0.70 [0.43–1.15]). Concomitant antiplatelet therapy was associated with higher bleeding (aHR 2.27 [1.38–3.73]) with no apparent reduction in MACNE (aHR 1.50 [1.00–2.25]). Conclusions: Most patients with AF and vascular disease were managed with oral anticoagulation. About half of them were also treated with concomitant antiplatelet therapy, which was associated with increased risk of bleeding, without evidence of improved cardiovascular outcomes.
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U2 - 10.1016/j.ahj.2019.04.007
DO - 10.1016/j.ahj.2019.04.007
M3 - Article
C2 - 31129441
AN - SCOPUS:85065922693
SN - 0002-8703
VL - 213
SP - 81
EP - 90
JO - American Heart Journal
JF - American Heart Journal
ER -