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Persistence with Anticoagulation for Atrial Fibrillation: Report from the GLORIA-AF Phase III 1-Year Follow-up.
Koziel, Monika; Mazurek, Michal; Teutsch, Christine; Diener, Hans-Christoph; Dubner, Sergio J; Halperin, Jonathan L; Ma, Chang-Sheng; Rothman, Kenneth J; Brandes, Axel; Paquette, Miney; Zint, Kristina; França, Lionel Riou; Lu, Shihai; Bartels, Dorothee B; Huisman, Menno V; Lip, Gregory Y H.
Afiliação
  • Koziel M; Liverpool Centre for Cardiovascular Science, University of Liverpool and Liverpool Heart & Chest Hospital, Liverpool L7 8TX, UK.
  • Mazurek M; 1st Department of Cardiology and Angiology, Silesian Centre for Heart Diseases, 41-800 Zabrze, Poland.
  • Teutsch C; 1st Department of Cardiology and Angiology, Silesian Centre for Heart Diseases, 41-800 Zabrze, Poland.
  • Diener HC; Department of Clinical Development and Medical Affairs, Therapeutic Area Cardiometabolism, Boehringer Ingelheim International GmbH, 55216 Ingelheim am Rhein, Germany.
  • Dubner SJ; Institute for Medical Informatics, Biometry and Epidemiology, University of Duisburg-Essen, 45133 Essen, Germany.
  • Halperin JL; Clínica y Maternidad Suizo Argentina, Buenos Aires C1420, Argentina.
  • Ma CS; Icahn School of Medicine at Mount Sinai, New York, NY 10001, USA.
  • Rothman KJ; Cardiology Department, Atrial Fibrillation Center, Beijing AnZhen Hospital, Capital Medical University, Beijing 100011, China.
  • Brandes A; RTI Health Solutions, Research Triangle Park, NC 27709, USA.
  • Paquette M; Department of Cardiology, Odense University Hospital, 5000 Odense, Denmark.
  • Zint K; Department of Medicine, Boehringer Ingelheim, Burlington, ON 05401, Canada.
  • França LR; Global Epidemiology Department, Boehringer Ingelheim International GmbH, 55216 Ingelheim am Rhein, Germany.
  • Lu S; Global Epidemiology Department, Boehringer Ingelheim International GmbH, 55216 Ingelheim am Rhein, Germany.
  • Bartels DB; Sanofi-Aventis Recherche et Development, 91380 Chilly-Mazarin, France.
  • Huisman MV; Biostatistics and Data Sciences Department, Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877, USA.
  • Lip GYH; Global Epidemiology Department, Boehringer Ingelheim International GmbH, 55216 Ingelheim am Rhein, Germany.
J Clin Med ; 9(6)2020 Jun 23.
Article em En | MEDLINE | ID: mdl-32586056
ABSTRACT

BACKGROUND:

We aimed to assess the extent to which drug persistence is better with non-vitamin K antagonist oral anticoagulants (NOACs) than vitamin K antagonists (VKAs) in atrial fibrillation (AF) patients and to estimate the difference in therapy persistence depending on NOAC dosing regimen (once daily (QD) vs. twice daily (BID)).

METHODS:

Consecutive patients were followed for 1 year in phase III of the GLORIA-AF registry. Drug persistence was defined as the use of OAC without any discontinuation in >30 days or switching to alternative therapy.

RESULTS:

Among 21,109 eligible patients in phase III, 17,266 patients who were prescribed OAC at baseline and those who took ≥1 OAC dose were included. The 1-year proportion of patients receiving NOAC and VKA who persisted on treatment was 80% and 75%, respectively. The 1-year persistence with NOACs BID and NOACs QD was 81% and 80%, respectively. Female gender, hypertension, older age, alcohol use, permanent, asymptomatic, and minimally symptomatic AF were associated with better OAC persistence. Region, medication usage predisposing to bleeding, being a current smoker, treatment reimbursement, and proton pump inhibitors were associated with lower OAC persistence.

CONCLUSIONS:

Drug persistence was higher with NOACs (1-year persistence was 80%) than with VKAs (75%). There was little difference in 1-year persistence between NOAC dosing regimens.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article