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Impact of Edoxaban on Thrombin-Dependent Platelet Aggregation
Edoxaban, a direct factor Xa inhibitor (FXa), is the fourth direct oral anticoagulant (DOAC) approved for clinical use. As the main adverse event is bleeding, it is relevant whether edoxaban has additional effects on platelet function. We aimed to assess in vitro aggregation in patients with atrial...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573709/ https://www.ncbi.nlm.nih.gov/pubmed/33054412 http://dx.doi.org/10.1177/1076029620948585 |
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author | Sokol, Juraj Nehaj, Frantisek Ivankova, Jela Mokan, Michal Lisa, Lenka Zolkova, Jana Vadelova, Lubica Mokan, Marian Stasko, Jan |
author_facet | Sokol, Juraj Nehaj, Frantisek Ivankova, Jela Mokan, Michal Lisa, Lenka Zolkova, Jana Vadelova, Lubica Mokan, Marian Stasko, Jan |
author_sort | Sokol, Juraj |
collection | PubMed |
description | Edoxaban, a direct factor Xa inhibitor (FXa), is the fourth direct oral anticoagulant (DOAC) approved for clinical use. As the main adverse event is bleeding, it is relevant whether edoxaban has additional effects on platelet function. We aimed to assess in vitro aggregation in patients with atrial fibrillation (AF) receiving edoxaban. We evaluated 20 AF patients treated with edoxaban. We assessed light transmittance platelet aggregation (LTA) with 100 nmol/L γ-thrombin. The LTA was performed at 2 time-points. The thrombin-induced platelet aggregation was significantly lower 2 hours after edoxaban was taken compared to baseline measurement (27.25% ± 30.8% vs. 60.35% ± 33.3%). In addition, we also performed 16 subanalyses in order to identify the differences in the outcome of different comorbidities, age, dosage, liver and kidney function tests, and concomitant treatment. Results of the subgroup analyses were consistent with the findings of the main analysis; there was no apparent heterogeneity across the prespecified subgroups. The thrombin-induced platelet aggregation is reduced in non-valvular AF patients receiving edoxaban. |
format | Online Article Text |
id | pubmed-7573709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-75737092020-10-27 Impact of Edoxaban on Thrombin-Dependent Platelet Aggregation Sokol, Juraj Nehaj, Frantisek Ivankova, Jela Mokan, Michal Lisa, Lenka Zolkova, Jana Vadelova, Lubica Mokan, Marian Stasko, Jan Clin Appl Thromb Hemost Original Article Edoxaban, a direct factor Xa inhibitor (FXa), is the fourth direct oral anticoagulant (DOAC) approved for clinical use. As the main adverse event is bleeding, it is relevant whether edoxaban has additional effects on platelet function. We aimed to assess in vitro aggregation in patients with atrial fibrillation (AF) receiving edoxaban. We evaluated 20 AF patients treated with edoxaban. We assessed light transmittance platelet aggregation (LTA) with 100 nmol/L γ-thrombin. The LTA was performed at 2 time-points. The thrombin-induced platelet aggregation was significantly lower 2 hours after edoxaban was taken compared to baseline measurement (27.25% ± 30.8% vs. 60.35% ± 33.3%). In addition, we also performed 16 subanalyses in order to identify the differences in the outcome of different comorbidities, age, dosage, liver and kidney function tests, and concomitant treatment. Results of the subgroup analyses were consistent with the findings of the main analysis; there was no apparent heterogeneity across the prespecified subgroups. The thrombin-induced platelet aggregation is reduced in non-valvular AF patients receiving edoxaban. SAGE Publications 2020-10-15 /pmc/articles/PMC7573709/ /pubmed/33054412 http://dx.doi.org/10.1177/1076029620948585 Text en © The Author(s) 2020 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 pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Sokol, Juraj Nehaj, Frantisek Ivankova, Jela Mokan, Michal Lisa, Lenka Zolkova, Jana Vadelova, Lubica Mokan, Marian Stasko, Jan Impact of Edoxaban on Thrombin-Dependent Platelet Aggregation |
title | Impact of Edoxaban on Thrombin-Dependent Platelet Aggregation |
title_full | Impact of Edoxaban on Thrombin-Dependent Platelet Aggregation |
title_fullStr | Impact of Edoxaban on Thrombin-Dependent Platelet Aggregation |
title_full_unstemmed | Impact of Edoxaban on Thrombin-Dependent Platelet Aggregation |
title_short | Impact of Edoxaban on Thrombin-Dependent Platelet Aggregation |
title_sort | impact of edoxaban on thrombin-dependent platelet aggregation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573709/ https://www.ncbi.nlm.nih.gov/pubmed/33054412 http://dx.doi.org/10.1177/1076029620948585 |
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