4.6 Article

Effects of the oral, direct factor Xa inhibitor apixaban on routine coagulation assays and anti-FXa assays

期刊

JOURNAL OF THROMBOSIS AND HAEMOSTASIS
卷 12, 期 9, 页码 1545-1553

出版社

WILEY-BLACKWELL
DOI: 10.1111/jth.12649

关键词

analysis; anticogaulants; apixaban; blood coagulation tests; factorXa

资金

  1. Bristol Meyers Squibb

向作者/读者索取更多资源

IntroductionApixaban is an oral direct factorXa inhibitor developed for the prophylaxis and treatment of thromboembolic disorders. Laboratory monitoring is not necessary, but the effects on common coagulation reagents and assays constitute clinically valuable information. ObjectivesTo investigate the effects of apixaban on commonly used coagulation methods, and to evaluate anti-FXa assays for specific determination of the drug concentration. Materials and MethodsApixaban was added to plasma from healthy subjects in the concentration range 0-1000gL(-1), and analyses were performed with different reagents for activated partial thromboplastin time (APTT), prothrombin time (PT), antithrombin, proteinC, and proteinS. A lupus anticoagulant assay and an APTT assay with varying phospholipid concentrations were used to study the phospholipid dependence. ResultsIn general, apixaban showed fewer effects invitro than have been shown for rivaroxaban, another direct FXa inhibitor. The concentration needed to double the APTT varied between 2200 and 4700gL(-1), and the concentration needed to double the PT varied between 700 and 3900gL(-1). The effects on antithrombin, proteinC and proteinS assays were dependent on the type of reagent. Apixaban did not cause false-positive lupus anticoagulant results. Chromogenic anti-FXa assays showed linear dose-response curves with apixaban. ConclusionsTherapeutic concentrations of apixaban variably affect different assay groups, and even different reagents within an assay group. The effects were much smaller than with rivaroxaban. The use of APTT and/or PT assays to screen the anticoagulant activity of apixaban cannot be recommended. A chromogenic anti-FXa assay can be used for reliable measurements of apixaban concentration.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Hematology

von Willebrand factor alloantibodies in type 3 von Willebrand disease

Barbara Faganel Kotnik, Karin Strandberg, Marusa Debeljak, Lidija Kitanovski, Janez Jazbec, Majda Benedik-Dolnicar, Alenka Trampus Bakija

BLOOD COAGULATION & FIBRINOLYSIS (2020)

Review Hematology

Clinical utility and impact of the use of the chromogenic vs one-stage factor activity assays in haemophilia A and B

Richard A. Marlar, Karin Strandberg, Midori Shima, Dorothy M. Adcock

EUROPEAN JOURNAL OF HAEMATOLOGY (2020)

Article Biotechnology & Applied Microbiology

Biomarker dynamics in cardiac surgery: a prospective observational study on MR-proADM, MR-proANP, hs-CRP and sP-selectin plasma levels in the perioperative period

Jonas Holm, Ingemar Cederholm, Urban Alehagen, Tomas L. Lindahl, Zoltan Szabo

BIOMARKERS (2020)

Article Hematology

Unveiling the complex effects of direct oral anticoagulants on dilute Russell's viper venom time assays

Andreas Hillarp, Karin Strandberg, Kerstin M. Gustafsson, Tomas L. Lindahl

JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2020)

Article Cell Biology

Sex differences in platelet reactivity in patients with myocardial infarction treated with triple antiplatelet therapy-results from assessing platelet activity in coronary heart disease (APACHE)

Anna Holm, Eva Swahn, Sofia Sederholm Lawesson, Kerstin M. Gustafsson, Magnus Janzon, Lena Jonasson, Tomas L. Lindahl, Joakim Alfredsson

Summary: In patients with myocardial infarction, women have a significantly higher rate of in-hospital bleeding events compared to men, although there were no significant differences in platelet aggregation between the sexes. The results do not support excess dosing of anti-platelet drugs as a major explanation for the increased bleeding risk in women.

PLATELETS (2021)

Article Hematology

Validation of factor VIII activity for monitoring standard and extended half-life products and correlation to thrombin generation assays

Cecilia Augustsson, Eva Norstrom, Vivian Lind, Myriam Martin, Jan Astermark, Karin Strandberg

Summary: The study validated the monitoring of different FVIII products on Atellica Coag, showing good correlation and acceptable bias between CSA-1 and OSA. There was a clear dose-response relationship between thrombin generation parameters and products.

HAEMOPHILIA (2021)

Article Nutrition & Dietetics

Dietary Supplementation with Selenium and Coenzyme Q10 Prevents Increase in Plasma D-Dimer While Lowering Cardiovascular Mortality in an Elderly Swedish Population

Urban Alehagen, Jan Aaseth, Tomas L. Lindahl, Anders Larsson, Jan Alexander

Summary: Supplementation with selenium and coenzyme Q(10) can reduce D-dimer levels and the risk of cardiovascular mortality. The study results demonstrate that supplementation can prevent an increase in D-dimer, lower cardiovascular mortality, and reveal important associations between inflammation, endothelial function, and cardiovascular risk.

NUTRIENTS (2021)

Article Medical Laboratory Technology

Evaluation of the Atellica COAG 360 coagulation analyzer in a specialized coagulation laboratory

Karin Strandberg, Cecilia Augustsson

Summary: This study evaluated the analytical performance of the Atellica COAG 360 analyzer in diagnosing bleeding disorders in a specialized coagulation laboratory. The results showed that the analyzer performed as expected and was equivalent to the BCS-XP in determining coagulation parameters, making it suitable for accurate diagnosis of bleeding disorders.

JOURNAL OF CLINICAL LABORATORY ANALYSIS (2022)

Article Cardiac & Cardiovascular Systems

Effects of Heparin and Bivalirudin on Thrombin-Induced Platelet Activation: Differential Modulation of PAR Signaling Drives Divergent Prothrombotic Responses

Mikael Lund, Ankit S. Macwan, Kjersti Tunstromer, Tomas L. Lindahl, Niklas Boknas

Summary: The study found that heparin and bivalirudin have different and complementary inhibitory effects on the activation of PAR1 and PAR4 by thrombin. Heparin inhibits PAR4-mediated platelet activation, while bivalirudin inhibits signaling from both receptors but leads to delayed PAR4-mediated platelet activation, resulting in a strong prothrombotic response.

FRONTIERS IN CARDIOVASCULAR MEDICINE (2021)

Article Hematology

Associations between hemostatic markers and mortality in COVID-19-Compounding effects of D-dimer, antithrombin and PAP complex

Niklas Boknas, Cia Laine, Andreas Hillarp, Ankit S. Macwan, Kerstin M. Gustafsson, Tomas L. Lindahl, Margareta Holmstrom

Summary: In this study, laboratory markers were used to characterize hemostatic function in COVID-19 patients. The incidence of death and venous thromboembolism in COVID-19 positive patients was significantly higher compared to COVID-19 negative patients. Elevated levels of von Willebrand factor and fibrinogen were observed in COVID-19 positive patients. In addition, abnormalities in specific hemostatic markers were associated with increased mortality in COVID-19 positive patients, particularly in cases with combined defects in markers of fibrinolysis and coagulation.

THROMBOSIS RESEARCH (2022)

Article Hematology

Methods for anti-factor VIII antibody levels in haemophilia A patients - validation of a multiplex immunoassay and comparability with assays measuring non-neutralising and neutralising antibodies (inhibitors)

Myriam Martin, Cecilia Augustsson, Vivian Lind, Riam Al-Sabti, My Chi Lam, Nadine G. Andersson, Karin Strandberg

Summary: The xFLI method, based on Luminex xMAP fluorescence-immunoassay, is more sensitive and reproducible than ELISA and CBA for detecting anti-FVIII antibodies in patients with haemophilia A. It can detect both functional inhibitors and non-neutralising antibodies accurately. The overall concordance between xFLI and ELISA was 82.1% and xFLI and CBA was 77.9%.

HAEMOPHILIA (2022)

Article Cell Biology

Thrombus remodelling by reversible and irreversible P2Y12 inhibitors

Kjersti Tunstromer, Lars Faxalv, Pia Larsson, Tomas L. Lindahl, Niklas Boknas

Summary: Pharmacological inhibition of the platelet ADP-receptor P2Y(12) is important in preventing atherothrombotic events. Our study compared the effects of two different P2Y(12) inhibitors and found that one had a slower but significant platelet inhibitory effect. Additionally, we observed that inhibited platelets gradually accumulated at the periphery of the thrombus.

PLATELETS (2023)

Article Hematology

Monitoring standard and extended half-life products in hemophilia: Assay discrepancies for factor VIII and IX in pre- and postinfusion samples

Cecilia Augustsson, Eva Norstrom, Nadine Gretenkort Andersson, Eva Zetterberg, Jan Astermark, Karin Strandberg

RESEARCH AND PRACTICE IN THROMBOSIS AND HAEMOSTASIS (2020)

暂无数据