Persistence with Anticoagulation for Atrial Fibrillation: Report from the GLORIA-AF Phase III 1-Year Follow-up

被引:12
|
作者
Koziel, Monika [1 ,2 ,3 ]
Mazurek, Michal [3 ]
Teutsch, Christine [4 ]
Diener, Hans-Christoph [5 ]
Dubner, Sergio J. [6 ]
Halperin, Jonathan L. [7 ]
Ma, Chang-Sheng [8 ]
Rothman, Kenneth J. [9 ]
Brandes, Axel [10 ]
Paquette, Miney [11 ]
Zint, Kristina [12 ]
Franca, Lionel Riou [12 ,13 ]
Lu, Shihai [14 ]
Bartels, Dorothee B. [12 ,15 ]
Huisman, Menno V. [16 ]
Lip, Gregory Y. H. [1 ,2 ,3 ,17 ]
机构
[1] Univ Liverpool, Liverpool Ctr Cardiovasc Sci, Liverpool L7 8TX, Merseyside, England
[2] Liverpool Heart & Chest Hosp, Liverpool L7 8TX, Merseyside, England
[3] Silesian Ctr Heart Dis, Dept Cardiol & Angiol 1, PL-41800 Zabrze, Poland
[4] Boehringer Ingelheim Int GmbH, Therapeut Area Cardiometab, Dept Clin Dev & Med Affairs, D-55216 Ingelheim, Germany
[5] Univ Duisburg Essen, Inst Med Informat Biometry & Epidemiol, D-45133 Essen, Germany
[6] Clin & Maternidad Suizo Argentina, RA-1420 Buenos Aires, DF, Argentina
[7] Icahn Sch Med Mt Sinai, New York, NY 10001 USA
[8] Capital Med Univ, Beijing AnZhen Hosp, Atrial Fibrillat Ctr, Cardiol Dept, Beijing 100011, Peoples R China
[9] RTI Hlth Solut, Res Triangle Pk, NC 27709 USA
[10] Odense Univ Hosp, Dept Cardiol, DK-5000 Odense, Denmark
[11] Boehringer Ingelheim GmbH & Co KG, Dept Med, Burlington, ON 05401, Canada
[12] Boehringer Ingelheim Int GmbH, Global Epidemiol Dept, D-55216 Ingelheim, Germany
[13] Sanofi Aventis Rech & Dev, F-91380 Chilly Mazarin, France
[14] Boehringer Ingelheim Pharmaceut Inc, Biostat & Data Sci Dept, Ridgefield, CT 06877 USA
[15] Hannover Med Sch, D-30159 Hannover, Germany
[16] Leiden Univ, Med Ctr, Dept Thrombosis & Hemostasis, NL-1043 AJ Leiden, Netherlands
[17] Aalborg Univ, Dept Clin Med, Aalborg Thrombosis Res Unit, DK-9000 Aalborg, Denmark
关键词
atrial fibrillation; dosing frequency; GLORIA-AF; non-vitamin K antagonist oral anticoagulants; oral anticoagulants; vitamin K antagonists; DOSING FREQUENCY; ORAL ANTICOAGULATION; STROKE PREVENTION; ADHERENCE; WARFARIN; RIVAROXABAN; DABIGATRAN; THERAPY; RISK; MEDICATIONS;
D O I
10.3390/jcm9061969
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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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页码:1 / 11
页数:11
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