Association of frailty and cognitive impairment with benefits of oral anticoagulation in patients with atrial fibrillation.


Journal

American heart journal
ISSN: 1097-6744
Titre abrégé: Am Heart J
Pays: United States
ID NLM: 0370465

Informations de publication

Date de publication:
05 2019
Historique:
received: 09 07 2018
accepted: 15 01 2019
pubmed: 23 3 2019
medline: 13 2 2020
entrez: 23 3 2019
Statut: ppublish

Résumé

The incidence of cognitive impairment and frailty increase with age and may impact both therapy and outcomes in atrial fibrillation (AF). We examined the prevalence of clinically recognized cognitive impairment and frailty (as defined by the American Geriatric Society Criteria) in the Outcomes Registry for Better Informed Care in AF (ORBIT AF) and associated adjusted outcomes via multivariable Cox regression. The interaction between cognitive impairment and frailty and oral anticoagulation (OAC) in determining outcomes was examined. Among 9749 patients with AF [median (IQR) age 75 (67-82) y, 57% male], cognitive impairment and frailty was identified in 293 (3.0%) and 575 (5.9%) patients respectively. Frail patients (68 vs 77%, P < .001) and those with cognitive impairment (70 vs 77%, P = .006) were both less likely to receive an OAC. Both cognitive impairment [HR (95% CI) 1.34 (1.05-1.72), P = .0198] and frailty [HR 1.29 (1.08-1.55), P = .0060] were associated with increased risk of death. Cognitive impairment and frailty were not associated with stroke/transient ischemic attack (TIA) or major bleeding. In multivariable analysis, there was no interaction between OAC use and cognitive impairment or frailty in their associations with mortality, major bleeding and a composite end point of stroke, non-central nervous system systemic embolism, TIA, myocardial infarction or cardiovascular death. Those with cognitive impairment or frailty in AF had higher predicted risk for stroke and higher observed mortality, yet were less likely to be treated with OAC. Despite this, the benefits of OAC were similar in patients with and without cognitive impairment or frailty.

Sections du résumé

BACKGROUND
The incidence of cognitive impairment and frailty increase with age and may impact both therapy and outcomes in atrial fibrillation (AF).
METHODS
We examined the prevalence of clinically recognized cognitive impairment and frailty (as defined by the American Geriatric Society Criteria) in the Outcomes Registry for Better Informed Care in AF (ORBIT AF) and associated adjusted outcomes via multivariable Cox regression. The interaction between cognitive impairment and frailty and oral anticoagulation (OAC) in determining outcomes was examined.
RESULTS
Among 9749 patients with AF [median (IQR) age 75 (67-82) y, 57% male], cognitive impairment and frailty was identified in 293 (3.0%) and 575 (5.9%) patients respectively. Frail patients (68 vs 77%, P < .001) and those with cognitive impairment (70 vs 77%, P = .006) were both less likely to receive an OAC. Both cognitive impairment [HR (95% CI) 1.34 (1.05-1.72), P = .0198] and frailty [HR 1.29 (1.08-1.55), P = .0060] were associated with increased risk of death. Cognitive impairment and frailty were not associated with stroke/transient ischemic attack (TIA) or major bleeding. In multivariable analysis, there was no interaction between OAC use and cognitive impairment or frailty in their associations with mortality, major bleeding and a composite end point of stroke, non-central nervous system systemic embolism, TIA, myocardial infarction or cardiovascular death.
CONCLUSION
Those with cognitive impairment or frailty in AF had higher predicted risk for stroke and higher observed mortality, yet were less likely to be treated with OAC. Despite this, the benefits of OAC were similar in patients with and without cognitive impairment or frailty.

Identifiants

pubmed: 30901602
pii: S0002-8703(19)30006-7
doi: 10.1016/j.ahj.2019.01.005
pii:
doi:

Substances chimiques

Anticoagulants 0

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

77-89

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Malini Madhavan (M)

Department of Cardiology, Mayo Clinic, Rochester, MN. Electronic address: Madhavan.malini@mayo.edu.

DaJuanicia N Holmes (DN)

Duke Clinical Research Institute, Durham, NC.

Jonathan P Piccini (JP)

Duke Clinical Research Institute, Durham, NC.

Jack E Ansell (JE)

New York University School of Medicine, Lenox Hill Hospital, New York.

Gregg C Fonarow (GC)

University of California, Los Angeles, CA.

Elaine M Hylek (EM)

Boston University School of Medicine, Boston, MA.

Peter R Kowey (PR)

Lankenau Heart Institute and the Jefferson Medical College, Philadelphia, PA.

Kenneth W Mahaffey (KW)

Stanford University School of Medicine, Palo Alto, CA.

Laine Thomas (L)

Duke Clinical Research Institute, Durham, NC.

Eric D Peterson (ED)

Duke Clinical Research Institute, Durham, NC.

Paul Chan (P)

University of Missouri-Kansas City School of Medicine, Kansas City, MO.

Larry A Allen (LA)

University of Colorado School of Medicine, Aurora, CO.

Bernard J Gersh (BJ)

Department of Cardiology, Mayo Clinic, Rochester, MN.

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