Apixaban vs warfarine chez les patients en FA et Insuffisance Rénale Chronique Terminale.

Titre original : 
Outcomes Associated with Apixaban Use in End-Stage Kidney Disease Patients with Atrial Fibrillation in the United States
Titre en français : 
Apixaban vs warfarine chez les patients en FA et Insuffisance Rénale Chronique Terminale.
Auteurs : 
Siontis KC, Zhang X, Eckard A, Bhave N, et al.
Revue : 
Circulation. 2018 Jun 28. pii: CIRCULATIONAHA.118.035418




Résumé : 

BACKGROUND : Patients with end-stage kidney disease (ESKD) on dialysis were excluded from clinical trials of direct oral anticoagulants for atrial fibrillation (AF). Recent data have raised concern regarding the safety of dabigatran and rivaroxaban, but apixaban has not been evaluated despite current labeling supporting its use in this population. The goal of this study was to determine patterns of apixaban use and its associated outcomes in dialysis-dependent ESKD patients with AF.
METHODS : We performed a retrospective cohort study of Medicare beneficiaries included in the United States Renal Data System (October 2010 to December 2015). Eligible patients were those with ESKD and AF undergoing dialysis who initiated treatment with an oral anticoagulant. Due to the small number of dabigatran and rivaroxaban users, outcomes were assessed only in patients treated with apixaban or warfarin. Apixaban and warfarin patients were matched (1:3) based on prognostic score. Differences between groups in survival free of stroke or systemic embolism, major bleeding, gastrointestinal bleeding, intracranial bleeding, and death were assessed using Kaplan-Meier analyses. Hazard ratios (HR) and 95% confidence intervals (CI) were derived from Cox regression analyses.
RESULTS : The study population consisted of 25,523 patients (45.7% women; age 68.2±11.9 years), including 2,351 patients on apixaban and 23,172 patients on warfarin. An annual increase in apixaban prescriptions was observed following its marketing approval in the end of 2012, such that 26.6% of new anticoagulant prescriptions in 2015 were for apixaban. In matched cohorts, there was no difference in the risks of stroke/systemic embolism between apixaban and warfarin (HR 0.88, 95% CI 0.69-1.12; P=0.29), but apixaban was associated with significantly lower risk of major bleeding (HR 0.72, 95% CI 0.59-0.87; P<0.001). In sensitivity analyses, standard dose apixaban (5 mg twice a day; n=1,034) was associated with significantly lower risks of stroke/systemic embolism and death as compared with either reduced dose apixaban (2.5 mg twice a day; n=1,317; HR 0.61, 95% CI 0.37-0.98, P=0.04 for stroke/systemic embolism; and HR 0.64, 95% CI 0.45-0.92, P=0.01 for death) or warfarin (HR 0.64, 95% CI 0.42-0.97, P=0.04 for stroke/systemic embolism; and HR 0.63, 95% CI 0.46-0.85, P=0.003 for death);
CONCLUSIONS : Among ESKD patients with AF on dialysis, apixaban use may be associated with lower risk of major bleeding compared with warfarin, with a standard 5 mg twice a day dose also associated with reductions in thromboembolic and mortality risk.