TY - JOUR
T1 - Association of frailty and cognitive impairment with benefits of oral anticoagulation in patients with atrial fibrillation
AU - on behalf of the ORBIT AF Investigators
AU - Madhavan, Malini
AU - Holmes, Da Juanicia N.
AU - Piccini, Jonathan P.
AU - Ansell, Jack E.
AU - Fonarow, Gregg C.
AU - Hylek, Elaine M.
AU - Kowey, Peter R.
AU - Mahaffey, Kenneth W.
AU - Thomas, Laine
AU - Peterson, Eric D.
AU - Chan, Paul
AU - Allen, Larry A.
AU - Gersh, Bernard J.
N1 - Funding Information:
M Madhavan: Consultant to Convatec. D Holmes: None. JP Piccini: ARCA biopharma, Boston Scientific, GE Healthcare, and Johnson & Johnson/Janssen Scientific Affairs and consultancies to Forest Laboratories, Janssen Scientific Affairs, Pfizer/ Bristol Myers Squibb, Spectranetics, and Medtronic. JE Ansell: Consultant activities and honoraria from: Bristol Myers Squibb, Pfizer, Daiichi Sankyo, Berhenger Ingelheim, Janssen, Instrumentation Laboratories, Perosphere Inc, Equity interest: Perosphere, Inc. GC Fonarow: consultant to Janssen. EM Hylek: honoraria, modest: Boehringer-Ingelheim, Bayer, and consultant/advisory board, modest: Daiichi Sankyo, Ortho-McNeil-Janssen, Johnson & Johnson, Boehringer-Ingelheim, Bristol-Myers Squibb. PR Kowey: Consultant J&J, Daiich-Sankyo, Bristol Myers Squibb, BI. KW Mahaffey: financial disclosures can be viewed at http://med.stanford.edu/profiles/kenneth-mahaffey . L Thomas: Participation in research with Novartis, Boston Scientific, Gilead Sciences, Inc, Janssen Scientific. ED Peterson: Research support from Eli Lilly & Company and Janssen. BJ Gersh: modest DSMB/Advisory Board support from Medtronic, Baxter Healthcare Corporation, InspireMD, Cardiovascular Research Foundation, PPD Development, LP, Boston Scientific, and St. Jude.
Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2019/5
Y1 - 2019/5
N2 - 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.
AB - 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.
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U2 - 10.1016/j.ahj.2019.01.005
DO - 10.1016/j.ahj.2019.01.005
M3 - Article
C2 - 30901602
AN - SCOPUS:85063065077
SN - 0002-8703
VL - 211
SP - 77
EP - 89
JO - American heart journal
JF - American heart journal
ER -