Apixaban concentration variability and relation to clinical outcomes in real-life patients with atrial fibrillation

Abstract In some clinical situations, measurements of anticoagulant effect of apixaban may be needed. We investigated the inter- and intra-individual apixaban variability in patients with atrial fibrillation and correlated these results with clinical outcome. We included 62 patients receiving either...

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Autores principales: Alenka Mavri, Nina Vene, Mojca Božič-Mijovski, Marko Miklič, Lisbeth Söderblom, Anton Pohanka, Rickard E. Malmström, Jovan Antovic
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/0924ed74aa5d49abbeb7d5aa319ba73a
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spelling oai:doaj.org-article:0924ed74aa5d49abbeb7d5aa319ba73a2021-12-02T18:34:20ZApixaban concentration variability and relation to clinical outcomes in real-life patients with atrial fibrillation10.1038/s41598-021-93372-92045-2322https://doaj.org/article/0924ed74aa5d49abbeb7d5aa319ba73a2021-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-93372-9https://doaj.org/toc/2045-2322Abstract In some clinical situations, measurements of anticoagulant effect of apixaban may be needed. We investigated the inter- and intra-individual apixaban variability in patients with atrial fibrillation and correlated these results with clinical outcome. We included 62 patients receiving either 5 mg (A5, n = 32) or 2.5 mg (A2.5, n = 30) apixaban twice-daily. We collected three trough and three peak blood samples 6–8 weeks apart. Apixaban concentration was measured by liquid chromatography-tandem mass-spectrometry (LC–MS/MS) and by anti-Xa. Patients on A2.5 were older, had lower creatinine clearance, higher CHA2DS2VASc (4.7 ± 1.0 vs. 3.4 ± 1.7) and lower trough (85 ± 39 vs. 117 ± 53 ng/mL) and peak (170 ± 56 vs. 256 ± 91 ng/mL) apixaban concentrations than patients on A5 (all p < 0.01). In patients on A5, LC–MS/MS showed a significant difference between through levels and between peak levels (p < 0.01). During apixaban treatment, 21 patients suffered bleeding (2 major). There was no association between bleeding and apixaban concentrations or variability. Four patients who suffered thromboembolic event had lower peak apixaban concentrations than patients without it (159 ± 13 vs. 238 ± 88 ng/mL, p = 0.05). We concluded, that there was a significant intra- and inter-individual variability in apixaban trough and peak concentrations. Neither variability nor apixaban concentrations were associated with clinical outcomes.Alenka MavriNina VeneMojca Božič-MijovskiMarko MikličLisbeth SöderblomAnton PohankaRickard E. MalmströmJovan AntovicNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-7 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Alenka Mavri
Nina Vene
Mojca Božič-Mijovski
Marko Miklič
Lisbeth Söderblom
Anton Pohanka
Rickard E. Malmström
Jovan Antovic
Apixaban concentration variability and relation to clinical outcomes in real-life patients with atrial fibrillation
description Abstract In some clinical situations, measurements of anticoagulant effect of apixaban may be needed. We investigated the inter- and intra-individual apixaban variability in patients with atrial fibrillation and correlated these results with clinical outcome. We included 62 patients receiving either 5 mg (A5, n = 32) or 2.5 mg (A2.5, n = 30) apixaban twice-daily. We collected three trough and three peak blood samples 6–8 weeks apart. Apixaban concentration was measured by liquid chromatography-tandem mass-spectrometry (LC–MS/MS) and by anti-Xa. Patients on A2.5 were older, had lower creatinine clearance, higher CHA2DS2VASc (4.7 ± 1.0 vs. 3.4 ± 1.7) and lower trough (85 ± 39 vs. 117 ± 53 ng/mL) and peak (170 ± 56 vs. 256 ± 91 ng/mL) apixaban concentrations than patients on A5 (all p < 0.01). In patients on A5, LC–MS/MS showed a significant difference between through levels and between peak levels (p < 0.01). During apixaban treatment, 21 patients suffered bleeding (2 major). There was no association between bleeding and apixaban concentrations or variability. Four patients who suffered thromboembolic event had lower peak apixaban concentrations than patients without it (159 ± 13 vs. 238 ± 88 ng/mL, p = 0.05). We concluded, that there was a significant intra- and inter-individual variability in apixaban trough and peak concentrations. Neither variability nor apixaban concentrations were associated with clinical outcomes.
format article
author Alenka Mavri
Nina Vene
Mojca Božič-Mijovski
Marko Miklič
Lisbeth Söderblom
Anton Pohanka
Rickard E. Malmström
Jovan Antovic
author_facet Alenka Mavri
Nina Vene
Mojca Božič-Mijovski
Marko Miklič
Lisbeth Söderblom
Anton Pohanka
Rickard E. Malmström
Jovan Antovic
author_sort Alenka Mavri
title Apixaban concentration variability and relation to clinical outcomes in real-life patients with atrial fibrillation
title_short Apixaban concentration variability and relation to clinical outcomes in real-life patients with atrial fibrillation
title_full Apixaban concentration variability and relation to clinical outcomes in real-life patients with atrial fibrillation
title_fullStr Apixaban concentration variability and relation to clinical outcomes in real-life patients with atrial fibrillation
title_full_unstemmed Apixaban concentration variability and relation to clinical outcomes in real-life patients with atrial fibrillation
title_sort apixaban concentration variability and relation to clinical outcomes in real-life patients with atrial fibrillation
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/0924ed74aa5d49abbeb7d5aa319ba73a
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