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Thrombin generation assays to personalize treatment in bleeding and thrombotic diseases
Treatment of bleeding and thrombotic disorders is highly standardized and based on evidence-based medicine guidelines. These evidence-based treatment schemes are well accepted but may lead to either insufficient treatment or over-dosing, because the individuals’ hemostatic properties are not taken i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684194/ https://www.ncbi.nlm.nih.gov/pubmed/36440026 http://dx.doi.org/10.3389/fcvm.2022.1033416 |
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author | Valke, Lars L. F. G. Rijpma, Sanna Meijer, Danielle Schols, Saskia E. M. van Heerde, Waander L. |
author_facet | Valke, Lars L. F. G. Rijpma, Sanna Meijer, Danielle Schols, Saskia E. M. van Heerde, Waander L. |
author_sort | Valke, Lars L. F. G. |
collection | PubMed |
description | Treatment of bleeding and thrombotic disorders is highly standardized and based on evidence-based medicine guidelines. These evidence-based treatment schemes are well accepted but may lead to either insufficient treatment or over-dosing, because the individuals’ hemostatic properties are not taken into account. This can potentially introduce bleeding or thrombotic complications in individual patients. With the incorporation of pharmacokinetic (PK) and pharmacodynamic (PK-PD) parameters, based on global assays such as thrombin generation assays (TGAs), a more personalized approach can be applied to treat either bleeding or thrombotic disorders. In this review, we will discuss the recent literature about the technical aspects of TGAs and the relation to diagnosis and management of bleeding and thrombotic disorders. In patients with bleeding disorders, such as hemophilia A or factor VII deficiency, TGAs can be used to identify patients with a more severe bleeding phenotype and also in the management with non-replacement therapy and/or bypassing therapy. These assays have also a role in patients with venous thrombo-embolism, but the usage of TGAs in patients with arterial thrombosis is less clear. However, there is a potential role for TGAs in the monitoring of (long-term) antithrombotic therapy, for example with the use of direct oral anticoagulants. Finally this review will discuss controversies, limitations and knowledge gaps in relation to the introduction of TGAs to personalize medicine in daily medical practice. |
format | Online Article Text |
id | pubmed-9684194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96841942022-11-25 Thrombin generation assays to personalize treatment in bleeding and thrombotic diseases Valke, Lars L. F. G. Rijpma, Sanna Meijer, Danielle Schols, Saskia E. M. van Heerde, Waander L. Front Cardiovasc Med Cardiovascular Medicine Treatment of bleeding and thrombotic disorders is highly standardized and based on evidence-based medicine guidelines. These evidence-based treatment schemes are well accepted but may lead to either insufficient treatment or over-dosing, because the individuals’ hemostatic properties are not taken into account. This can potentially introduce bleeding or thrombotic complications in individual patients. With the incorporation of pharmacokinetic (PK) and pharmacodynamic (PK-PD) parameters, based on global assays such as thrombin generation assays (TGAs), a more personalized approach can be applied to treat either bleeding or thrombotic disorders. In this review, we will discuss the recent literature about the technical aspects of TGAs and the relation to diagnosis and management of bleeding and thrombotic disorders. In patients with bleeding disorders, such as hemophilia A or factor VII deficiency, TGAs can be used to identify patients with a more severe bleeding phenotype and also in the management with non-replacement therapy and/or bypassing therapy. These assays have also a role in patients with venous thrombo-embolism, but the usage of TGAs in patients with arterial thrombosis is less clear. However, there is a potential role for TGAs in the monitoring of (long-term) antithrombotic therapy, for example with the use of direct oral anticoagulants. Finally this review will discuss controversies, limitations and knowledge gaps in relation to the introduction of TGAs to personalize medicine in daily medical practice. Frontiers Media S.A. 2022-11-10 /pmc/articles/PMC9684194/ /pubmed/36440026 http://dx.doi.org/10.3389/fcvm.2022.1033416 Text en Copyright © 2022 Valke, Rijpma, Meijer, Schols and van Heerde. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cardiovascular Medicine Valke, Lars L. F. G. Rijpma, Sanna Meijer, Danielle Schols, Saskia E. M. van Heerde, Waander L. Thrombin generation assays to personalize treatment in bleeding and thrombotic diseases |
title | Thrombin generation assays to personalize treatment in bleeding and thrombotic diseases |
title_full | Thrombin generation assays to personalize treatment in bleeding and thrombotic diseases |
title_fullStr | Thrombin generation assays to personalize treatment in bleeding and thrombotic diseases |
title_full_unstemmed | Thrombin generation assays to personalize treatment in bleeding and thrombotic diseases |
title_short | Thrombin generation assays to personalize treatment in bleeding and thrombotic diseases |
title_sort | thrombin generation assays to personalize treatment in bleeding and thrombotic diseases |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684194/ https://www.ncbi.nlm.nih.gov/pubmed/36440026 http://dx.doi.org/10.3389/fcvm.2022.1033416 |
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