Risk of Cardiovascular Events and Mortality Among Elderly Patients With Reduced GFR Receiving Direct Oral Anticoagulants.


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
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

311-320

Subventions

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.

Auteurs

Justin Ashley (J)

Department of Medicine, University of Ottawa, Ottawa.

Eric McArthur (E)

Institute for Clinical Evaluative Sciences, Ontario.

Sarah Bota (S)

Institute for Clinical Evaluative Sciences, Ontario.

Ziv Harel (Z)

Section of Nephrology, University of Toronto, Toronto.

Marissa Battistella (M)

Department of Pharmacy, University of Toronto, Toronto.

Amber O Molnar (AO)

Institute for Clinical Evaluative Sciences, Ontario; Section of Nephrology, McMaster University, Hamilton, Canada.

Min Jun (M)

The George Institute for Global Health, University of New South Wales, Sydney, Australia.

Sunil V Badve (SV)

The George Institute for Global Health, University of New South Wales, Sydney, Australia; Department of Nephrology, St George Hospital, Sydney, Australia.

Amit X Garg (AX)

Institute for Clinical Evaluative Sciences, Ontario; Section of Nephrology, Western University, London.

Doug Manuel (D)

Institute for Clinical Evaluative Sciences, Ontario; Departments of Family Medicine, University of Ottawa, Ottawa, Canada.

Peter Tanuseputro (P)

Institute for Clinical Evaluative Sciences, Ontario; Departments of Family Medicine, University of Ottawa, Ottawa, Canada; Departments of Public Health, University of Ottawa, Ottawa, Canada.

Phil Wells (P)

Section of Hematology, University of Ottawa, Ottawa, Canada.

Thomas Mavrakanas (T)

Division of General Internal Medicine, Geneva University Hospitals, Geneva, Switzerland.

Emily Rhodes (E)

Department of Medicine, University of Ottawa, Ottawa.

Manish M Sood (MM)

Department of Medicine, University of Ottawa, Ottawa; Division of General Internal Medicine, Geneva University Hospitals, Geneva, Switzerland; Section of Nephrology, University of Ottawa, Ottawa, Canada. Electronic address: msood@toh.on.ca.

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Classifications MeSH