Oral anticoagulation for stroke prevention in atrial fibrillation and advanced kidney disease

Research output: Contribution to journalJournal articleResearchpeer-review

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Oral anticoagulation for stroke prevention in atrial fibrillation and advanced kidney disease. / Ballegaard, Ellen Linnea Freese; Olesen, Jonas Bjerring; Kamper, Anne Lise; Feldt-Rasmussen, Bo; Gislason, Gunnar; Torp-Pedersen, Christian; Carlson, Nicholas.

In: Research and Practice in Thrombosis and Haemostasis, Vol. 8, No. 2, 102350, 2024.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Ballegaard, ELF, Olesen, JB, Kamper, AL, Feldt-Rasmussen, B, Gislason, G, Torp-Pedersen, C & Carlson, N 2024, 'Oral anticoagulation for stroke prevention in atrial fibrillation and advanced kidney disease', Research and Practice in Thrombosis and Haemostasis, vol. 8, no. 2, 102350. https://doi.org/10.1016/j.rpth.2024.102350

APA

Ballegaard, E. L. F., Olesen, J. B., Kamper, A. L., Feldt-Rasmussen, B., Gislason, G., Torp-Pedersen, C., & Carlson, N. (2024). Oral anticoagulation for stroke prevention in atrial fibrillation and advanced kidney disease. Research and Practice in Thrombosis and Haemostasis, 8(2), [102350]. https://doi.org/10.1016/j.rpth.2024.102350

Vancouver

Ballegaard ELF, Olesen JB, Kamper AL, Feldt-Rasmussen B, Gislason G, Torp-Pedersen C et al. Oral anticoagulation for stroke prevention in atrial fibrillation and advanced kidney disease. Research and Practice in Thrombosis and Haemostasis. 2024;8(2). 102350. https://doi.org/10.1016/j.rpth.2024.102350

Author

Ballegaard, Ellen Linnea Freese ; Olesen, Jonas Bjerring ; Kamper, Anne Lise ; Feldt-Rasmussen, Bo ; Gislason, Gunnar ; Torp-Pedersen, Christian ; Carlson, Nicholas. / Oral anticoagulation for stroke prevention in atrial fibrillation and advanced kidney disease. In: Research and Practice in Thrombosis and Haemostasis. 2024 ; Vol. 8, No. 2.

Bibtex

@article{d4d262beb6f44aa58f99539d1f491286,
title = "Oral anticoagulation for stroke prevention in atrial fibrillation and advanced kidney disease",
abstract = "Background: The net benefit of oral anticoagulation (OAC) with vitamin K antagonists or direct oral anticoagulants in patients with advanced chronic kidney disease and atrial fibrillation remains uncertain. Objectives: We examined the use, efficacy, and safety of OAC in patients with estimated glomerular filtration rate (eGFR) of <30 mL/min/1.73 m2 (including dialysis-treated patients) and atrial fibrillation. Methods: In a retrospective cohort study, patients diagnosed with atrial fibrillation and eGFR of <30 mL/min/1.73 m2 were identified in national Danish registers between 2010 and 2022. Initiation of OAC was identified based on redemption of a relevant prescription. One-year risks of thromboembolic event, major bleeding, and death associated with OAC and no treatment were computed and standardized to the distribution of risk factors in the sample based on hazards determined in multiple Cox regression models adjusted for age and sex. Results: A total of 3208 patients were included (mean age 80 years, 52.8% males, 20.9% chronic dialysis). OAC was initiated in 1375 (42.9%) patients, of whom 48.1% were vitamin K antagonists and 51.9% were direct oral anticoagulants. One-year risks in nontreated and anticoagulated patients were 4.8% (95% CI, 3.8%-5.7%) and 3.6% (95% CI, 2.8%-4.6%; P = .028) for thromboembolic event, 7.6% (95% CI, 6.6%-8.7%) and 10.5% (95% CI, 9.3%-12.1%; P < .001) for major bleeding, and 36.3% (95% CI, 34.2%-38.3%) and 29.6% (95% CI, 27.6%-31.6%; P < .001) for death, respectively. Conclusion: In a retrospective study on patients with advanced chronic kidney disease and atrial fibrillation, OAC was associated with overall decreased 1-year risk of thromboembolic event and death offset by increased 1-year risk of major bleeding.",
keywords = "anticoagulants, atrial fibrillation, hemorrhage, renal dialysis, thromboembolism",
author = "Ballegaard, {Ellen Linnea Freese} and Olesen, {Jonas Bjerring} and Kamper, {Anne Lise} and Bo Feldt-Rasmussen and Gunnar Gislason and Christian Torp-Pedersen and Nicholas Carlson",
note = "Publisher Copyright: {\textcopyright} 2024 The Author(s)",
year = "2024",
doi = "10.1016/j.rpth.2024.102350",
language = "English",
volume = "8",
journal = "Research and Practice in Thrombosis and Haemostasis",
issn = "2475-0379",
publisher = "Wiley",
number = "2",

}

RIS

TY - JOUR

T1 - Oral anticoagulation for stroke prevention in atrial fibrillation and advanced kidney disease

AU - Ballegaard, Ellen Linnea Freese

AU - Olesen, Jonas Bjerring

AU - Kamper, Anne Lise

AU - Feldt-Rasmussen, Bo

AU - Gislason, Gunnar

AU - Torp-Pedersen, Christian

AU - Carlson, Nicholas

N1 - Publisher Copyright: © 2024 The Author(s)

PY - 2024

Y1 - 2024

N2 - Background: The net benefit of oral anticoagulation (OAC) with vitamin K antagonists or direct oral anticoagulants in patients with advanced chronic kidney disease and atrial fibrillation remains uncertain. Objectives: We examined the use, efficacy, and safety of OAC in patients with estimated glomerular filtration rate (eGFR) of <30 mL/min/1.73 m2 (including dialysis-treated patients) and atrial fibrillation. Methods: In a retrospective cohort study, patients diagnosed with atrial fibrillation and eGFR of <30 mL/min/1.73 m2 were identified in national Danish registers between 2010 and 2022. Initiation of OAC was identified based on redemption of a relevant prescription. One-year risks of thromboembolic event, major bleeding, and death associated with OAC and no treatment were computed and standardized to the distribution of risk factors in the sample based on hazards determined in multiple Cox regression models adjusted for age and sex. Results: A total of 3208 patients were included (mean age 80 years, 52.8% males, 20.9% chronic dialysis). OAC was initiated in 1375 (42.9%) patients, of whom 48.1% were vitamin K antagonists and 51.9% were direct oral anticoagulants. One-year risks in nontreated and anticoagulated patients were 4.8% (95% CI, 3.8%-5.7%) and 3.6% (95% CI, 2.8%-4.6%; P = .028) for thromboembolic event, 7.6% (95% CI, 6.6%-8.7%) and 10.5% (95% CI, 9.3%-12.1%; P < .001) for major bleeding, and 36.3% (95% CI, 34.2%-38.3%) and 29.6% (95% CI, 27.6%-31.6%; P < .001) for death, respectively. Conclusion: In a retrospective study on patients with advanced chronic kidney disease and atrial fibrillation, OAC was associated with overall decreased 1-year risk of thromboembolic event and death offset by increased 1-year risk of major bleeding.

AB - Background: The net benefit of oral anticoagulation (OAC) with vitamin K antagonists or direct oral anticoagulants in patients with advanced chronic kidney disease and atrial fibrillation remains uncertain. Objectives: We examined the use, efficacy, and safety of OAC in patients with estimated glomerular filtration rate (eGFR) of <30 mL/min/1.73 m2 (including dialysis-treated patients) and atrial fibrillation. Methods: In a retrospective cohort study, patients diagnosed with atrial fibrillation and eGFR of <30 mL/min/1.73 m2 were identified in national Danish registers between 2010 and 2022. Initiation of OAC was identified based on redemption of a relevant prescription. One-year risks of thromboembolic event, major bleeding, and death associated with OAC and no treatment were computed and standardized to the distribution of risk factors in the sample based on hazards determined in multiple Cox regression models adjusted for age and sex. Results: A total of 3208 patients were included (mean age 80 years, 52.8% males, 20.9% chronic dialysis). OAC was initiated in 1375 (42.9%) patients, of whom 48.1% were vitamin K antagonists and 51.9% were direct oral anticoagulants. One-year risks in nontreated and anticoagulated patients were 4.8% (95% CI, 3.8%-5.7%) and 3.6% (95% CI, 2.8%-4.6%; P = .028) for thromboembolic event, 7.6% (95% CI, 6.6%-8.7%) and 10.5% (95% CI, 9.3%-12.1%; P < .001) for major bleeding, and 36.3% (95% CI, 34.2%-38.3%) and 29.6% (95% CI, 27.6%-31.6%; P < .001) for death, respectively. Conclusion: In a retrospective study on patients with advanced chronic kidney disease and atrial fibrillation, OAC was associated with overall decreased 1-year risk of thromboembolic event and death offset by increased 1-year risk of major bleeding.

KW - anticoagulants

KW - atrial fibrillation

KW - hemorrhage

KW - renal dialysis

KW - thromboembolism

U2 - 10.1016/j.rpth.2024.102350

DO - 10.1016/j.rpth.2024.102350

M3 - Journal article

AN - SCOPUS:85186726262

VL - 8

JO - Research and Practice in Thrombosis and Haemostasis

JF - Research and Practice in Thrombosis and Haemostasis

SN - 2475-0379

IS - 2

M1 - 102350

ER -

ID: 385024582