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Predictors of NOAC versus VKA use for stroke prevention in patients with newly diagnosed atrial fibrillation: Results from GARFIELD-AF - 16/06/19

Doi : 10.1016/j.ahj.2019.03.013 
Sylvia Haas a, , A John Camm b, Jean-Pierre Bassand c, d, Pantep Angchaisuksiri e, Frank Cools f, Ramon Corbalan g, Harry Gibbs h, Barry Jacobson i, Yukihiro Koretsune j, Lorenzo G Mantovani k, Frank Misselwitz l, Elizaveta Panchenko m, Hany Ibrahim Ragy n, Janina Stepinska o, Alexander GG Turpie p, Jitendra PS Sawhney q, Jan Steffel r, Toon Wei Lim s, Karen S Pieper d, t, Saverio Virdone d, Freek WA Verheugt u, Ajay K Kakkar d, v

for the GARFIELD-AF Investigators1

  A complete list of investigators is given in the Appendix.

a Formerly Technical University of Munich, Munich, Germany 
b Molecular and Clinical Sciences Research Institute, Cardiology Clinical Academic Group, St George's University of London, London, United Kingdom 
c University of Besançon, Besançon, France 
d Thrombosis Research Institute, London, United Kingdom 
e Ramathibodi Hospital, Mahidol University, Bangkok, Thailand 
f AZ Klina, Brasschaat, Belgium 
g Catholic University, Santiago, Chile 
h The Alfred Hospital, Melbourne, Australia 
i NHLS and University of the Witwatersrand, Charlotte Maxeke Hospital, Johannesburg, South Africa 
j National Hospital Organization, Osaka National Hospital, Osaka, Japan 
k University of Milano-Bicocca, Milan, Italy 
l Bayer AG, Pharmaceuticals, Berlin, Germany 
m Russian Cardiology Research and Production Center, Department of Atherothrombosis, 3-d Cherepkovskaya str., 15 A, Moscow, Russian Federation 
n National Heart Institute, Cairo, Egypt 
o Institute of Cardiology, Warsaw, Poland 
p McMaster University, Hamilton, Canada 
q Sir Ganga Ram Hospital, New Delhi, India 
r University Hospital Zurich, Zurich, Switzerland 
s National University Heart Centre, Singapore (NUHCS), 1E Kent Ridge Road, NUHS Tower Block, Level 9, Singapore, Republic of Singapore 
t Duke Clinical Research Institute, Durham, NC, USA 
u Onze Lieve Vrouwe Gasthuis (OLVG), Amsterdam, The Netherlands 
v University College London, London, United Kingdom 

Reprint requests: Sylvia Haas, Emeritus Professor and Senior Consultant, Technical University of Munich, Munich, Germany.Emeritus Professor and Senior Consultant, Technical University of MunichMunichGermany

Abstract

Introduction

A principal aim of the Global Anticoagulant Registry in the FIELD-Atrial Fibrillation (GARFIELD-AF) was to document changes in treatment practice for patients with newly diagnosed atrial fibrillation during an era when non–vitamin K antagonist oral anticoagulants (NOACs) were becoming more widely adopted. In these analyses, the key factors which determined the choice between NOACs and vitamin K antagonists (VKAs) are explored.

Methods

Logistic least absolute shrinkage and selection operator regression determined predictors of NOAC and VKA use. Data were collected from 24,137 patients who were initiated on AC ± antiplatelet (AP) therapy (NOAC [51.4%] or VKA [48.6%]) between April 2013 and August 2016.

Results

The most significant predictors of AC therapy were country, enrolment year, care setting at diagnosis, AF type, concomitant AP, and kidney disease. Patients enrolled in emergency care or in the outpatient setting were more likely to receive a NOAC than those enrolled in hospital (OR 1.16 [95% CI: 1.04-1.30], OR: 1.15 [95% CI: 1.05-1.25], respectively). NOAC prescribing seemed to be favored in lower-risk groups, namely, patients with paroxysmal AF, normotensive patients, and those with moderate alcohol consumption, but also the elderly and patients with acute coronary syndrome. By contrast, VKAs were preferentially used in patients with permanent AF, moderate to severe kidney disease, heart failure, vascular disease, and diabetes and with concomitant AP.

Conclusion

GARFIELD-AF data highlight marked heterogeneity in stroke prevention strategies globally. Physicians are adopting an individualized approach to stroke prevention where NOACs are favored in patients with a lower stroke risk but also in the elderly and patients with acute coronary syndrome.

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Plan


 Clinical Trial Registration: URL: www.clinicaltrials.gov. Unique identifier: NCT01090362.
 Funding: This work was supported by an unrestricted research grant from Bayer AG (Berlin, Germany) to the Thrombosis Research Institute (London, UK), which sponsors the GARFIELD-AF registry. The funding source had no involvement in the data collection, data analysis, or data interpretation.


© 2019  The Authors. Publié par Elsevier Masson SAS. Tous droits réservés.
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Vol 213

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