Počet záznamů: 1  

Effect of Apixaban Pretreatment on Alteplase-Induced Thrombolysis: An In Vitro Study

  1. 1.
    SYSNO ASEP0546625
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevEffect of Apixaban Pretreatment on Alteplase-Induced Thrombolysis: An In Vitro Study
    Tvůrce(i) Thalerova, S. (CZ)
    Pešková, Michaela (BFU-R)
    Kittová, Patrícia (BFU-R)
    Gulati, S. (CZ)
    Víteček, Jan (BFU-R) RID, ORCID
    Kubala, Lukáš (BFU-R) RID, ORCID
    Mikulik, R. (CZ)
    Celkový počet autorů7
    Číslo článku740930
    Zdroj.dok.Frontiers in Pharmacology. - : Frontiers Media - ISSN 1663-9812
    Roč. 12, SEP 15 2021 (2021)
    Poč.str.8 s.
    Forma vydáníOnline - E
    Jazyk dok.eng - angličtina
    Země vyd.CH - Švýcarsko
    Klíč. slovaantagonist oral anticoagulants ; acute ischemic-stroke ; plasminogen-activator ; intravenous thrombolysis ; warfarin ; clot
    Vědní obor RIVFR - Farmakologie a lékárnická chemie
    Obor OECDPharmacology and pharmacy
    Způsob publikováníOpen access
    Institucionální podporaBFU-R - RVO:68081707
    UT WOS000701295900001
    EID SCOPUS85116001307
    DOI10.3389/fphar.2021.740930
    AnotaceBenefit of thrombolytic therapy in patients with acute stroke, who are on anticoagulant treatment, is not well addressed. The aim of this study was to investigate whether apixaban can modify the thrombolytic efficacy of alteplase in vitro. Static and flow models and two variants of red blood cell (RBC) dominant clots, with and without apixaban, were used. Clots were prepared from the blood of healthy human donors and subsequently exposed to alteplase treatment. Apixaban and alteplase were used in clinically relevant concentrations. Clot lysis in the static model was determined both by clot weight and spectrophotometric determination of RBC release. Clot lysis in the flow model was determined by measuring recanalization time, clot length and spectrophotometric determination of RBC release. In the static model, clots without apixaban, compared to those with apixaban had alteplase-induced mass loss 54 +/- 8% vs. 53 +/- 8%, p = 1.00, RBC release 0.14 +/- 0.04 vs. 0.12 +/- 0.04, p = 0.14, respectively. Very similar results were obtained if plasma was used instead of physiological buffered saline as the incubation medium. In the flow model, clot lysis without apixaban, compared to those with apixaban was as follows: recanalization time 107 +/- 46 min vs. 127 +/- 31 min, p = 1.00, recanalization frequency 90 +/- 22% vs. 90 +/- 22%, p = 1.00, clot volume reduction 32 +/- 15% vs. 34 +/- 10%, p = 1.00, RBC release 0.029 +/- 0.007 vs. 0.022 +/- 0.007, p = 0.16, respectively. Apixaban had no positive effect on alteplase-induced thrombolysis in both the in vitro static and flow models. Our data support current clinical practice, such that thrombolysis is contraindicated in stroke treatment for patients who have been treated with anticoagulants./p
    PracovištěBiofyzikální ústav
    KontaktJana Poláková, polakova@ibp.cz, Tel.: 541 517 244
    Rok sběru2022
    Elektronická adresahttps://www.frontiersin.org/articles/10.3389/fphar.2021.740930/full
Počet záznamů: 1  

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