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Risk of overanticoagulation during acute kidney injury in patients treated with vitamin K antagonists

BACKGROUND: Vitamin K antagonists (VKAs) are still in use for oral anticoagulation, but not all indications allow their replacement by direct oral anticoagulants. Although formal dose reduction is not required in patients with impaired kidney function, case reports indicate that acute kidney injury...

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Autores principales: Süfling, Luisa, Greinert, Daniel, Girndt, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8951229/
https://www.ncbi.nlm.nih.gov/pubmed/33459792
http://dx.doi.org/10.1093/ndt/gfab008
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author Süfling, Luisa
Greinert, Daniel
Girndt, Matthias
author_facet Süfling, Luisa
Greinert, Daniel
Girndt, Matthias
author_sort Süfling, Luisa
collection PubMed
description BACKGROUND: Vitamin K antagonists (VKAs) are still in use for oral anticoagulation, but not all indications allow their replacement by direct oral anticoagulants. Although formal dose reduction is not required in patients with impaired kidney function, case reports indicate that acute kidney injury (AKI) might be associated with derailment of VKA therapy. METHODS: The study retrospectively collected patients from a tertiary nephrology care centre who experienced AKI while being treated with VKA. In these individuals, the international normalized ratio (INR) as a measure of anticoagulant effect during renal failure was compared with a reference time point with stable kidney function. RESULTS: A total of 100 patients with AKI and ongoing VKA therapy met the inclusion criteria. The majority (76%) of patients had AKI with CKD. Volume depletion (n = 43), septic renal failure (n = 22), decompensated heart failure (n = 18) and toxic renal damage (n = 11) were the most important causes of AKI. The average INR values at the time of AKI were higher than at the reference time point [median 3.17 (range 1.10–13.0) versus 2.24 (1.07–5.17); P < 0.0001]. Fifty-four patients had INR values above the recommended therapeutic range for their indication at the time point of AKI. Bleeding complications occurred in 24 patients during AKI and the VKA dose had to be reduced in 55. Women, patients with low body mass index and patients with diabetes were predisposed to overanticoagulation during AKI. CONCLUSIONS: The effect of AKI on anticoagulation by VKA has not been systematically described. This risk should be considered in patients at high risk for AKI.
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spelling pubmed-89512292022-03-28 Risk of overanticoagulation during acute kidney injury in patients treated with vitamin K antagonists Süfling, Luisa Greinert, Daniel Girndt, Matthias Nephrol Dial Transplant Original Article BACKGROUND: Vitamin K antagonists (VKAs) are still in use for oral anticoagulation, but not all indications allow their replacement by direct oral anticoagulants. Although formal dose reduction is not required in patients with impaired kidney function, case reports indicate that acute kidney injury (AKI) might be associated with derailment of VKA therapy. METHODS: The study retrospectively collected patients from a tertiary nephrology care centre who experienced AKI while being treated with VKA. In these individuals, the international normalized ratio (INR) as a measure of anticoagulant effect during renal failure was compared with a reference time point with stable kidney function. RESULTS: A total of 100 patients with AKI and ongoing VKA therapy met the inclusion criteria. The majority (76%) of patients had AKI with CKD. Volume depletion (n = 43), septic renal failure (n = 22), decompensated heart failure (n = 18) and toxic renal damage (n = 11) were the most important causes of AKI. The average INR values at the time of AKI were higher than at the reference time point [median 3.17 (range 1.10–13.0) versus 2.24 (1.07–5.17); P < 0.0001]. Fifty-four patients had INR values above the recommended therapeutic range for their indication at the time point of AKI. Bleeding complications occurred in 24 patients during AKI and the VKA dose had to be reduced in 55. Women, patients with low body mass index and patients with diabetes were predisposed to overanticoagulation during AKI. CONCLUSIONS: The effect of AKI on anticoagulation by VKA has not been systematically described. This risk should be considered in patients at high risk for AKI. Oxford University Press 2021-01-18 /pmc/articles/PMC8951229/ /pubmed/33459792 http://dx.doi.org/10.1093/ndt/gfab008 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the ERA. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Süfling, Luisa
Greinert, Daniel
Girndt, Matthias
Risk of overanticoagulation during acute kidney injury in patients treated with vitamin K antagonists
title Risk of overanticoagulation during acute kidney injury in patients treated with vitamin K antagonists
title_full Risk of overanticoagulation during acute kidney injury in patients treated with vitamin K antagonists
title_fullStr Risk of overanticoagulation during acute kidney injury in patients treated with vitamin K antagonists
title_full_unstemmed Risk of overanticoagulation during acute kidney injury in patients treated with vitamin K antagonists
title_short Risk of overanticoagulation during acute kidney injury in patients treated with vitamin K antagonists
title_sort risk of overanticoagulation during acute kidney injury in patients treated with vitamin k antagonists
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8951229/
https://www.ncbi.nlm.nih.gov/pubmed/33459792
http://dx.doi.org/10.1093/ndt/gfab008
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