Suscribirse

Comparative Stroke, Bleeding, and Mortality Risks in Older Medicare Patients Treated with Oral Anticoagulants for Nonvalvular Atrial Fibrillation - 07/05/19

Doi : 10.1016/j.amjmed.2018.12.023 
David J. Graham, MD, MPH a, , Elande Baro, PhD b, Rongmei Zhang, PhD b, Jiemin Liao, MA c, Michael Wernecke, BA c, Marsha E. Reichman, PhD a, Mao Hu, BS c, Onyekachukwu Illoh, OD, MPH a, Yuqin Wei, MS c, Margie R. Goulding, PhD a, Yoganand Chillarige, MPA c, Mary Ross Southworth, PharmD d, Thomas E. MaCurdy, PhD c, e, Jeffrey A. Kelman, MD, MMSc f
a Office of Surveillance and Epidemiology, Center for Drug Evaluation and Research 
b Office of Biostatistics, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, Md 
c Acumen LLC, Burlingame, Calif 
d Office of New Drugs, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, Md 
e Department of Economics, Stanford University, Stanford, Calif 
f Centers for Medicare & Medicaid Services, Washington, DC 

Requests for reprints should be addressed to David J. Graham, MD, MPH, Office of Surveillance and Epidemiology, 10903 New Hampshire Ave, Building 22, Room 4314, Silver Spring, MD, 20993-0002.Office of Surveillance and Epidemiology10903 New Hampshire Ave, Building 22, Room 4314Silver SpringMD20993-0002

Abstract

Background

Nonvitamin K antagonist oral anticoagulants (NOACs) are alternatives to warfarin in patients with nonvalvular atrial fibrillation. Randomized trials compared NOACs with warfarin, but none have compared individual NOACs against each other for safety and effectiveness.

Methods

We performed a retrospective new-user cohort study of patients with nonvalvular atrial fibrillation enrolled in US Medicare who initiated warfarin (n = 183,318), or a standard dose of dabigatran (150 mg twice daily; n = 86,198), rivaroxaban (20 mg once daily; n = 106,389), or apixaban (5 mg twice daily; n = 73,039) between October 2010 and September 2015. Propensity score-adjusted Cox proportional hazards regression was used to estimate adjusted hazard ratios (HR) and 95% confidence intervals (CI) for the outcomes of thromboembolic stroke, intracranial hemorrhage, major extracranial bleeding, and all-cause mortality, comparing each NOAC with warfarin, and with each other NOAC.

Results

Compared with warfarin, each NOAC was associated with reduced risks of thromboembolic stroke (20%-29% reduction; P = .002 [dabigatran], P < 0.001 [rivaroxaban, apixaban]), intracranial hemorrhage (35%-62% reduction; P < 0.001 [each NOAC]), and mortality (19%-34% reduction; P < .001 [each NOAC]). The NOACs were similar for thromboembolic stroke but rivaroxaban was associated with increased risks of intracranial hemorrhage (vs dabigatran: HR = 1.71; 95% CI, 1.35-2.17), major extracranial bleeding (vs dabigatran: HR = 1.32; 95% CI, 1.21-1.45; vs apixaban: HR = 2.70; 95% CI, 2.38-3.05), and death (vs dabigatran: HR = 1.12; 95% CI, 1.01-1.24; vs apixaban: HR = 1.23; 95% CI, 1.09-1.38). Dabigatran was associated with reduced risk of intracranial hemorrhage (HR = 0.70; 95% CI ,0.53-0.94) and increased risk of major extracranial bleeding (HR = 2.04; 95% CI, 1.78-2.32) compared with apixaban.

Conclusions

Among patients treated with standard-dose NOAC for nonvalvular atrial fibrillation and warfarin users with similar baseline characteristics, dabigatran, rivaroxaban, and apixaban were associated with a more favorable benefit–harm profile than warfarin. Among NOAC users, dabigatran and apixaban were associated with a more favorable benefit–harm profile than rivaroxaban.

El texto completo de este artículo está disponible en PDF.

Keywords : Anticoagulants, Apixaban, Atrial fibrillation, Comparative effectiveness, Comparative safety, Dabigatran, Rivaroxaban, Warfarin


Esquema


 Funding: The US Food and Drug Administration, through an interagency agreement between it and the Centers for Medicare & Medicaid Services.
 Conflict of Interest: None of the authors have any conflicts of interest to declare.
 Authorship: All authors had access to the data and a role in writing the manuscript. The views expressed are the authors’ and not necessarily those of the Centers for Medicare & Medicaid Services, the Food and Drug Administration, or the Department of Health and Human Services.


© 2019  Elsevier Inc. Reservados todos los derechos.
Añadir a mi biblioteca Eliminar de mi biblioteca Imprimir
Exportación

    Exportación citas

  • Fichero

  • Contenido

Vol 132 - N° 5

P. 596 - mai 2019 Regresar al número
Artículo precedente Artículo precedente
  • Magnitude of Venous Thromboembolism Risk in US Hospitals: Impact of Evolving National Guidelines for Prevention of Venous Thromboembolism
  • Wei Huang, Alexander T. Cohen, Anne-Céline Martin, Frederick A. Anderson
| Artículo siguiente Artículo siguiente
  • Young Adults and Adverse Childhood Events: A Potent Measure of Cardiovascular Risk
  • Catherine Kreatsoulas, Eric W. Fleegler, Laura D Kubzansky, Catherine M. McGorrian, Subu V. Subramanian

Bienvenido a EM-consulte, la referencia de los profesionales de la salud.
El acceso al texto completo de este artículo requiere una suscripción.

¿Ya suscrito a @@106933@@ revista ?

@@150455@@ Voir plus

Mi cuenta


Declaración CNIL

EM-CONSULTE.COM se declara a la CNIL, la declaración N º 1286925.

En virtud de la Ley N º 78-17 del 6 de enero de 1978, relativa a las computadoras, archivos y libertades, usted tiene el derecho de oposición (art.26 de la ley), el acceso (art.34 a 38 Ley), y correcta (artículo 36 de la ley) los datos que le conciernen. Por lo tanto, usted puede pedir que se corrija, complementado, clarificado, actualizado o suprimido información sobre usted que son inexactos, incompletos, engañosos, obsoletos o cuya recogida o de conservación o uso está prohibido.
La información personal sobre los visitantes de nuestro sitio, incluyendo su identidad, son confidenciales.
El jefe del sitio en el honor se compromete a respetar la confidencialidad de los requisitos legales aplicables en Francia y no de revelar dicha información a terceros.


Todo el contenido en este sitio: Copyright © 2026 Elsevier, sus licenciantes y colaboradores. Se reservan todos los derechos, incluidos los de minería de texto y datos, entrenamiento de IA y tecnologías similares. Para todo el contenido de acceso abierto, se aplican los términos de licencia de Creative Commons.