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Impact of Vitamin K Administration on Elevated International Normalized Ratio in Chronic Liver Disease

Limited studies assess the efficacy of vitamin K administration in patients with chronic liver disease (CLD). However, vitamin K is commonly used to treat elevations in international normalized ratio (INR) in these patients with the intended benefit of reducing bleeding risk. This retrospective, sin...

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Autores principales: Smith, Carmen B., Hennessey, Erin K., Crossey, Caroline D., Crannage, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10134161/
https://www.ncbi.nlm.nih.gov/pubmed/37093741
http://dx.doi.org/10.1177/10760296231164642
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author Smith, Carmen B.
Hennessey, Erin K.
Crossey, Caroline D.
Crannage, Andrew J.
author_facet Smith, Carmen B.
Hennessey, Erin K.
Crossey, Caroline D.
Crannage, Andrew J.
author_sort Smith, Carmen B.
collection PubMed
description Limited studies assess the efficacy of vitamin K administration in patients with chronic liver disease (CLD). However, vitamin K is commonly used to treat elevations in international normalized ratio (INR) in these patients with the intended benefit of reducing bleeding risk. This retrospective, single-center cohort study aimed to evaluate the impact of vitamin K administration on INR in patients with CLD. Hospitalized patients ≥ 18 years of age with a diagnosis of CLD or cirrhosis and received vitamin K were included. The primary outcome was the absolute change in INR from baseline to 24 to 48 h after vitamin K administration. Secondary endpoints included subgroup analyses of the primary outcome by route of administration and single versus multidose administration, and incidence of in-hospital venous thromboembolism (VTE) or major bleeding. A total of eighty-five patients, primarily with Child–Pugh class C (76.5%), were included. Route of vitamin K administration included oral (PO) (72%) and intravenous (IV) (26%) with a mean daily dose of 8.5 ± 2.3 mg. The absolute change in INR was −0.07 ± −0.35 following vitamin K administration. There was no difference in absolute INR change between single versus multiple dose administration (−0.16 ± −0.35 and −0.03 ± −0.35; P= .13) or between PO versus IV administration (−0.06 ± −0.23 and −0.18 ± −0.48; P = .11). The incidences of in-hospital VTE and major bleeding were 2.4% and 3.5%, respectively. The administration of vitamin K in hospitalized patients with CLD resulted in minimal INR change, suggesting this intervention may not have the intended benefit of reducing bleeding risk.
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spelling pubmed-101341612023-04-28 Impact of Vitamin K Administration on Elevated International Normalized Ratio in Chronic Liver Disease Smith, Carmen B. Hennessey, Erin K. Crossey, Caroline D. Crannage, Andrew J. Clin Appl Thromb Hemost Original Article Limited studies assess the efficacy of vitamin K administration in patients with chronic liver disease (CLD). However, vitamin K is commonly used to treat elevations in international normalized ratio (INR) in these patients with the intended benefit of reducing bleeding risk. This retrospective, single-center cohort study aimed to evaluate the impact of vitamin K administration on INR in patients with CLD. Hospitalized patients ≥ 18 years of age with a diagnosis of CLD or cirrhosis and received vitamin K were included. The primary outcome was the absolute change in INR from baseline to 24 to 48 h after vitamin K administration. Secondary endpoints included subgroup analyses of the primary outcome by route of administration and single versus multidose administration, and incidence of in-hospital venous thromboembolism (VTE) or major bleeding. A total of eighty-five patients, primarily with Child–Pugh class C (76.5%), were included. Route of vitamin K administration included oral (PO) (72%) and intravenous (IV) (26%) with a mean daily dose of 8.5 ± 2.3 mg. The absolute change in INR was −0.07 ± −0.35 following vitamin K administration. There was no difference in absolute INR change between single versus multiple dose administration (−0.16 ± −0.35 and −0.03 ± −0.35; P= .13) or between PO versus IV administration (−0.06 ± −0.23 and −0.18 ± −0.48; P = .11). The incidences of in-hospital VTE and major bleeding were 2.4% and 3.5%, respectively. The administration of vitamin K in hospitalized patients with CLD resulted in minimal INR change, suggesting this intervention may not have the intended benefit of reducing bleeding risk. SAGE Publications 2023-04-24 /pmc/articles/PMC10134161/ /pubmed/37093741 http://dx.doi.org/10.1177/10760296231164642 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Smith, Carmen B.
Hennessey, Erin K.
Crossey, Caroline D.
Crannage, Andrew J.
Impact of Vitamin K Administration on Elevated International Normalized Ratio in Chronic Liver Disease
title Impact of Vitamin K Administration on Elevated International Normalized Ratio in Chronic Liver Disease
title_full Impact of Vitamin K Administration on Elevated International Normalized Ratio in Chronic Liver Disease
title_fullStr Impact of Vitamin K Administration on Elevated International Normalized Ratio in Chronic Liver Disease
title_full_unstemmed Impact of Vitamin K Administration on Elevated International Normalized Ratio in Chronic Liver Disease
title_short Impact of Vitamin K Administration on Elevated International Normalized Ratio in Chronic Liver Disease
title_sort impact of vitamin k administration on elevated international normalized ratio in chronic liver disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10134161/
https://www.ncbi.nlm.nih.gov/pubmed/37093741
http://dx.doi.org/10.1177/10760296231164642
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