Antithrombotic Treatment in Patients With Heart Failure and Associated Atrial Fibrillation and Vascular Disease : A Nationwide Cohort Study

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Antithrombotic Treatment in Patients With Heart Failure and Associated Atrial Fibrillation and Vascular Disease : A Nationwide Cohort Study. / Lamberts, Morten; Lip, Gregory Y H; Ruwald, Martin H; Hansen, Morten Lock; Özcan, Cengiz; Kristensen, Søren L; Køber, Lars; Torp-Pedersen, Christian; Gislason, Gunnar H.

In: Journal of the American College of Cardiology, Vol. 63, No. 24, 24.06.2014, p. 2689–2698.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Lamberts, M, Lip, GYH, Ruwald, MH, Hansen, ML, Özcan, C, Kristensen, SL, Køber, L, Torp-Pedersen, C & Gislason, GH 2014, 'Antithrombotic Treatment in Patients With Heart Failure and Associated Atrial Fibrillation and Vascular Disease : A Nationwide Cohort Study', Journal of the American College of Cardiology, vol. 63, no. 24, pp. 2689–2698. https://doi.org/10.1016/j.jacc.2014.03.039

APA

Lamberts, M., Lip, G. Y. H., Ruwald, M. H., Hansen, M. L., Özcan, C., Kristensen, S. L., Køber, L., Torp-Pedersen, C., & Gislason, G. H. (2014). Antithrombotic Treatment in Patients With Heart Failure and Associated Atrial Fibrillation and Vascular Disease : A Nationwide Cohort Study. Journal of the American College of Cardiology, 63(24), 2689–2698. https://doi.org/10.1016/j.jacc.2014.03.039

Vancouver

Lamberts M, Lip GYH, Ruwald MH, Hansen ML, Özcan C, Kristensen SL et al. Antithrombotic Treatment in Patients With Heart Failure and Associated Atrial Fibrillation and Vascular Disease : A Nationwide Cohort Study. Journal of the American College of Cardiology. 2014 Jun 24;63(24):2689–2698. https://doi.org/10.1016/j.jacc.2014.03.039

Author

Lamberts, Morten ; Lip, Gregory Y H ; Ruwald, Martin H ; Hansen, Morten Lock ; Özcan, Cengiz ; Kristensen, Søren L ; Køber, Lars ; Torp-Pedersen, Christian ; Gislason, Gunnar H. / Antithrombotic Treatment in Patients With Heart Failure and Associated Atrial Fibrillation and Vascular Disease : A Nationwide Cohort Study. In: Journal of the American College of Cardiology. 2014 ; Vol. 63, No. 24. pp. 2689–2698.

Bibtex

@article{595db78953ee43598d07c14d1e47965d,
title = "Antithrombotic Treatment in Patients With Heart Failure and Associated Atrial Fibrillation and Vascular Disease :: A Nationwide Cohort Study",
abstract = "OBJECTIVES: The aim of this study was to investigate the impact of atrial fibrillation (AF) and antithrombotic treatment on the prognosis in patients with heart failure (HF) as well as vascular disease.BACKGROUND: HF, vascular disease, and AF are pathophysiologically related, and understanding antithrombotic treatment for these conditions is crucial.METHODS: In hospitalized patients with HF and coexisting vascular disease (coronary artery disease or peripheral arterial disease) followed from 1997 to 2009, AF status was categorized as prevalent AF, incident AF, or no AF. Risk of thromboembolism (TE), myocardial infarction (MI), and serious bleeding was assessed by Cox regression models (hazard ratio [HR] with 95% confidence interval [CI]) with antithrombotic therapy and AF as time-dependent variables.RESULTS: A total of 37,464 patients were included (age, 74.5 ± 10.7 years; 36.3% females) with a mean follow-up of 3 years during which 20.7% were categorized as prevalent AF and 17.2% as incident AF. Compared with vitamin K antagonist (VKA) in prevalent AF, VKA plus antiplatelet was not associated with a decreased risk of TE (HR: 0.91; 95% CI: 0.73 to 1.12) or MI (HR: 1.11; 95% CI: 0.96 to 1.28), whereas bleeding risk was significantly increased (HR: 1.31; 95% CI: 1.09 to 1.57). Corresponding estimates for incident AF were HRs of 0.77 (95% CI: 0.56 to 1.06), 1.07 (95% CI: 0.89 to 1.28), and 2.71 (95% CI: 1.33 to 2.21) for TE, MI, and bleeding, respectively. In no AF patients, no statistical differences were seen between antithrombotic therapies in TE or MI risk, whereas bleeding risk was significantly increased for VKA with and without single-antiplatelet therapy.CONCLUSIONS: In AF patients with coexisting HF and vascular disease, adding single-antiplatelet therapy to VKA therapy is not associated with additional benefit in thromboembolic or coronary risk, but notably increased bleeding risk.",
keywords = "Aged, Aged, 80 and over, Atrial Fibrillation, Cohort Studies, Denmark, Female, Fibrinolytic Agents, Follow-Up Studies, Heart Failure, Hospitalization, Humans, Male, Middle Aged, Registries, Retrospective Studies, Treatment Outcome, Vascular Diseases",
author = "Morten Lamberts and Lip, {Gregory Y H} and Ruwald, {Martin H} and Hansen, {Morten Lock} and Cengiz {\"O}zcan and Kristensen, {S{\o}ren L} and Lars K{\o}ber and Christian Torp-Pedersen and Gislason, {Gunnar H}",
note = "Copyright {\textcopyright} 2014 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.",
year = "2014",
month = jun,
day = "24",
doi = "10.1016/j.jacc.2014.03.039",
language = "English",
volume = "63",
pages = "2689–2698",
journal = "Journal of the American College of Cardiology",
issn = "0735-1097",
publisher = "Elsevier",
number = "24",

}

RIS

TY - JOUR

T1 - Antithrombotic Treatment in Patients With Heart Failure and Associated Atrial Fibrillation and Vascular Disease :

T2 - A Nationwide Cohort Study

AU - Lamberts, Morten

AU - Lip, Gregory Y H

AU - Ruwald, Martin H

AU - Hansen, Morten Lock

AU - Özcan, Cengiz

AU - Kristensen, Søren L

AU - Køber, Lars

AU - Torp-Pedersen, Christian

AU - Gislason, Gunnar H

N1 - Copyright © 2014 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

PY - 2014/6/24

Y1 - 2014/6/24

N2 - OBJECTIVES: The aim of this study was to investigate the impact of atrial fibrillation (AF) and antithrombotic treatment on the prognosis in patients with heart failure (HF) as well as vascular disease.BACKGROUND: HF, vascular disease, and AF are pathophysiologically related, and understanding antithrombotic treatment for these conditions is crucial.METHODS: In hospitalized patients with HF and coexisting vascular disease (coronary artery disease or peripheral arterial disease) followed from 1997 to 2009, AF status was categorized as prevalent AF, incident AF, or no AF. Risk of thromboembolism (TE), myocardial infarction (MI), and serious bleeding was assessed by Cox regression models (hazard ratio [HR] with 95% confidence interval [CI]) with antithrombotic therapy and AF as time-dependent variables.RESULTS: A total of 37,464 patients were included (age, 74.5 ± 10.7 years; 36.3% females) with a mean follow-up of 3 years during which 20.7% were categorized as prevalent AF and 17.2% as incident AF. Compared with vitamin K antagonist (VKA) in prevalent AF, VKA plus antiplatelet was not associated with a decreased risk of TE (HR: 0.91; 95% CI: 0.73 to 1.12) or MI (HR: 1.11; 95% CI: 0.96 to 1.28), whereas bleeding risk was significantly increased (HR: 1.31; 95% CI: 1.09 to 1.57). Corresponding estimates for incident AF were HRs of 0.77 (95% CI: 0.56 to 1.06), 1.07 (95% CI: 0.89 to 1.28), and 2.71 (95% CI: 1.33 to 2.21) for TE, MI, and bleeding, respectively. In no AF patients, no statistical differences were seen between antithrombotic therapies in TE or MI risk, whereas bleeding risk was significantly increased for VKA with and without single-antiplatelet therapy.CONCLUSIONS: In AF patients with coexisting HF and vascular disease, adding single-antiplatelet therapy to VKA therapy is not associated with additional benefit in thromboembolic or coronary risk, but notably increased bleeding risk.

AB - OBJECTIVES: The aim of this study was to investigate the impact of atrial fibrillation (AF) and antithrombotic treatment on the prognosis in patients with heart failure (HF) as well as vascular disease.BACKGROUND: HF, vascular disease, and AF are pathophysiologically related, and understanding antithrombotic treatment for these conditions is crucial.METHODS: In hospitalized patients with HF and coexisting vascular disease (coronary artery disease or peripheral arterial disease) followed from 1997 to 2009, AF status was categorized as prevalent AF, incident AF, or no AF. Risk of thromboembolism (TE), myocardial infarction (MI), and serious bleeding was assessed by Cox regression models (hazard ratio [HR] with 95% confidence interval [CI]) with antithrombotic therapy and AF as time-dependent variables.RESULTS: A total of 37,464 patients were included (age, 74.5 ± 10.7 years; 36.3% females) with a mean follow-up of 3 years during which 20.7% were categorized as prevalent AF and 17.2% as incident AF. Compared with vitamin K antagonist (VKA) in prevalent AF, VKA plus antiplatelet was not associated with a decreased risk of TE (HR: 0.91; 95% CI: 0.73 to 1.12) or MI (HR: 1.11; 95% CI: 0.96 to 1.28), whereas bleeding risk was significantly increased (HR: 1.31; 95% CI: 1.09 to 1.57). Corresponding estimates for incident AF were HRs of 0.77 (95% CI: 0.56 to 1.06), 1.07 (95% CI: 0.89 to 1.28), and 2.71 (95% CI: 1.33 to 2.21) for TE, MI, and bleeding, respectively. In no AF patients, no statistical differences were seen between antithrombotic therapies in TE or MI risk, whereas bleeding risk was significantly increased for VKA with and without single-antiplatelet therapy.CONCLUSIONS: In AF patients with coexisting HF and vascular disease, adding single-antiplatelet therapy to VKA therapy is not associated with additional benefit in thromboembolic or coronary risk, but notably increased bleeding risk.

KW - Aged

KW - Aged, 80 and over

KW - Atrial Fibrillation

KW - Cohort Studies

KW - Denmark

KW - Female

KW - Fibrinolytic Agents

KW - Follow-Up Studies

KW - Heart Failure

KW - Hospitalization

KW - Humans

KW - Male

KW - Middle Aged

KW - Registries

KW - Retrospective Studies

KW - Treatment Outcome

KW - Vascular Diseases

U2 - 10.1016/j.jacc.2014.03.039

DO - 10.1016/j.jacc.2014.03.039

M3 - Journal article

C2 - 24794118

VL - 63

SP - 2689

EP - 2698

JO - Journal of the American College of Cardiology

JF - Journal of the American College of Cardiology

SN - 0735-1097

IS - 24

ER -

ID: 138423360