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Vitamin K antagonist use: evidence of the difficulty of achieving and maintaining target INR range and subsequent consequences
Vitamin K antagonists (VKAs) are effective oral anticoagulants that are titrated to a narrow therapeutic international normalized ratio (INR) range. We reviewed published literature assessing the impact of INR stability - getting into and staying in target INR range - on outcomes including thromboti...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906845/ https://www.ncbi.nlm.nih.gov/pubmed/27303213 http://dx.doi.org/10.1186/s12959-016-0088-y |
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author | Schein, Jeff R. White, C. Michael Nelson, Winnie W. Kluger, Jeffrey Mearns, Elizabeth S. Coleman, Craig I. |
author_facet | Schein, Jeff R. White, C. Michael Nelson, Winnie W. Kluger, Jeffrey Mearns, Elizabeth S. Coleman, Craig I. |
author_sort | Schein, Jeff R. |
collection | PubMed |
description | Vitamin K antagonists (VKAs) are effective oral anticoagulants that are titrated to a narrow therapeutic international normalized ratio (INR) range. We reviewed published literature assessing the impact of INR stability - getting into and staying in target INR range - on outcomes including thrombotic events, major bleeding, and treatment costs, as well as key factors that impact INR stability. A time in therapeutic range (TTR) of ≥65 % is commonly accepted as the definition of INR stability. In the real-world setting, this is seldom achieved with standard-of-care management, thus increasing the patients’ risks of thrombotic or major bleeding events. There are many factors associated with poor INR control. Being treated in community settings, newly initiated on a VKA, younger in age, or nonadherent to therapy, as well as having polymorphisms of CYP2C9 or VKORC1, or multiple physical or mental co-morbid disease states have been associated with lower TTR. Clinical prediction tools are available, though they can only explain <10 % of the variance behind poor INR control. Clinicians caring for patients who require anticoagulation are encouraged to intensify diligence in INR management when using VKAs and to consider appropriate use of newer anticoagulants as a therapeutic option. |
format | Online Article Text |
id | pubmed-4906845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49068452016-06-15 Vitamin K antagonist use: evidence of the difficulty of achieving and maintaining target INR range and subsequent consequences Schein, Jeff R. White, C. Michael Nelson, Winnie W. Kluger, Jeffrey Mearns, Elizabeth S. Coleman, Craig I. Thromb J Review Vitamin K antagonists (VKAs) are effective oral anticoagulants that are titrated to a narrow therapeutic international normalized ratio (INR) range. We reviewed published literature assessing the impact of INR stability - getting into and staying in target INR range - on outcomes including thrombotic events, major bleeding, and treatment costs, as well as key factors that impact INR stability. A time in therapeutic range (TTR) of ≥65 % is commonly accepted as the definition of INR stability. In the real-world setting, this is seldom achieved with standard-of-care management, thus increasing the patients’ risks of thrombotic or major bleeding events. There are many factors associated with poor INR control. Being treated in community settings, newly initiated on a VKA, younger in age, or nonadherent to therapy, as well as having polymorphisms of CYP2C9 or VKORC1, or multiple physical or mental co-morbid disease states have been associated with lower TTR. Clinical prediction tools are available, though they can only explain <10 % of the variance behind poor INR control. Clinicians caring for patients who require anticoagulation are encouraged to intensify diligence in INR management when using VKAs and to consider appropriate use of newer anticoagulants as a therapeutic option. BioMed Central 2016-06-13 /pmc/articles/PMC4906845/ /pubmed/27303213 http://dx.doi.org/10.1186/s12959-016-0088-y Text en © Schein et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Schein, Jeff R. White, C. Michael Nelson, Winnie W. Kluger, Jeffrey Mearns, Elizabeth S. Coleman, Craig I. Vitamin K antagonist use: evidence of the difficulty of achieving and maintaining target INR range and subsequent consequences |
title | Vitamin K antagonist use: evidence of the difficulty of achieving and maintaining target INR range and subsequent consequences |
title_full | Vitamin K antagonist use: evidence of the difficulty of achieving and maintaining target INR range and subsequent consequences |
title_fullStr | Vitamin K antagonist use: evidence of the difficulty of achieving and maintaining target INR range and subsequent consequences |
title_full_unstemmed | Vitamin K antagonist use: evidence of the difficulty of achieving and maintaining target INR range and subsequent consequences |
title_short | Vitamin K antagonist use: evidence of the difficulty of achieving and maintaining target INR range and subsequent consequences |
title_sort | vitamin k antagonist use: evidence of the difficulty of achieving and maintaining target inr range and subsequent consequences |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906845/ https://www.ncbi.nlm.nih.gov/pubmed/27303213 http://dx.doi.org/10.1186/s12959-016-0088-y |
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