Risk of Cardiovascular Events and Mortality Among Elderly Patients With Reduced GFR Receiving Direct Oral Anticoagulants.
Aged
Aged, 80 and over
Antithrombins
/ adverse effects
Brain Ischemia
/ epidemiology
Cause of Death
Comorbidity
Dabigatran
/ adverse effects
Female
Glomerular Filtration Rate
Hemorrhage
/ chemically induced
Humans
Male
Mortality
Myocardial Infarction
/ epidemiology
Myocardial Revascularization
Ontario
/ epidemiology
Procedures and Techniques Utilization
Propensity Score
Proportional Hazards Models
Pyrazoles
/ adverse effects
Pyridones
/ adverse effects
Renal Insufficiency, Chronic
/ complications
Retrospective Studies
Rivaroxaban
/ adverse effects
Thrombophilia
/ complications
Vitamin K
/ antagonists & inhibitors
Direct oral anticoagulants (DOACs)
anticoagulation
cardiovascular events
chronic kidney disease (CKD)
estimated glomerular filtration rate (eGFR)
hemorrhage
kidney function
vitamin K antagonists (VKAs)
warfarin
Journal
American journal of kidney diseases : the official journal of the National Kidney Foundation
ISSN: 1523-6838
Titre abrégé: Am J Kidney Dis
Pays: United States
ID NLM: 8110075
Informations de publication
Date de publication:
09 2020
09 2020
Historique:
received:
24
07
2019
accepted:
11
02
2020
pubmed:
26
4
2020
medline:
9
10
2020
entrez:
26
4
2020
Statut:
ppublish
Résumé
Evidence for the efficacy of direct oral anticoagulants (DOACs) to prevent cardiovascular (CV) events and mortality in older individuals with a low estimated glomerular filtration rate (eGFR) is lacking. We sought to characterize the association of oral anticoagulant use with CV morbidity in elderly patients with or without reductions in eGFRs, comparing DOACs with vitamin K antagonists (VKAs). Population-based retrospective cohort study. All individuals 66 years or older with an initial prescription for oral anticoagulants dispensed in Ontario, Canada, from 2009 to 2016. DOACs (apixaban, dabigatran, and rivaroxaban) compared with VKAs by eGFR group (≥60, 30-59, and<30mL/min/1.73m The primary outcome was a composite of a CV event (myocardial infarction, revascularization, or ischemic stroke) or mortality. Secondary outcomes were CV events alone, mortality, and hemorrhage requiring hospitalization. High-dimensional propensity score matching of DOAC to VKA users and Cox proportional hazards regression. 27,552 new DOAC users were matched to 27,552 new VKA users (median age, 78 years; 49% women). There was significantly lower risk for CV events or mortality among DOAC users compared with VKA users (event rates of 79.78 vs 99.77 per 1,000 person-years, respectively; HR, 0.82 [95% CI, 0.75-0.90]) and lower risk for hemorrhage (event rates of 10.35 vs 16.77 per 1,000 person-years, respectively; HR, 0.73 [95% CI, 0.58-0.91]). There was an interaction between eGFR and the association of anticoagulant class with the primary composite outcome (P<0.02): HRs of 1.01 [95% CI, 0.92-1.12], 0.83 [95% CI, 0.75-0.93], and 0.75 [95% CI, 0.51-1.10] for eGFRs of≥60, 30 to 59, and<30mL/min/1.73m Retrospective observational study design limits causal inference; dosages of DOACs and international normalized ratio values were not available; low event rates in some subgroups limited statistical power. DOACs compared with VKAs were associated with lower risk for the composite of CV events or mortality, an association for which the strength was most apparent among those with reduced eGFRs. The therapeutic implications of these findings await further study.
Identifiants
pubmed: 32333946
pii: S0272-6386(20)30639-9
doi: 10.1053/j.ajkd.2020.02.446
pii:
doi:
Substances chimiques
Antithrombins
0
Pyrazoles
0
Pyridones
0
Vitamin K
12001-79-5
apixaban
3Z9Y7UWC1J
Rivaroxaban
9NDF7JZ4M3
Dabigatran
I0VM4M70GC
Types de publication
Comparative Study
Journal Article
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
311-320Subventions
Organisme : CIHR
Pays : Canada
Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2020 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.