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Browsing by Author "Mikovic, Danijela (35585598700)"

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    Publication
    Correlation to FVIII: C in two thrombin generation tests: TGA-CAT and INNOVANCE ETP
    (2017)
    Ljungkvist, Marcus (57193167894)
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    Berndtsson, Maria (6603376446)
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    Holmström, Margareta (7006841518)
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    Mikovic, Danijela (35585598700)
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    Elezovic, Ivo (12782840600)
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    Antovic, Jovan P. (6701874787)
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    Zetterberg, Eva (7801409763)
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    Berntorp, Erik (55145811700)
    Introduction: Several thrombin-generation tests are available, but few have been directly compared. Our primary aim was to investigate the correlation of two thrombin generation tests, thrombin generation assay-calibrated automated thrombogram (TGA-CAT) and INNOVANCE ETP, to factor VIII levels (FVIII:C) in a group of patients with hemophilia A. The secondary aim was to investigate inter-laboratory variation for the TGA-CAT method. Methods: Blood samples were taken from 45 patients with mild, moderate and severe hemophilia A. The TGA-CAT method was performed at both centers while the INNOVANCE ETP was only performed at the Stockholm center. Correlation between parameters was evaluated using Spearman's rank correlation test. For determination of the TGA-CAT inter-laboratory variability, Bland-Altman plots were used. Results: The correlation for the INNOVANCE ETP and TGA-CAT methods with FVIII:C in persons with hemophilia (PWH) was r=0.701 and r=0.734 respectively. The correlation between the two methods was r=0.546. When dividing the study material into disease severity groups (mild, moderate and severe) based on FVIII levels, both methods fail to discriminate between them. The variability of the TGA-CAT results performed at the two centers was reduced after normalization; before normalization, 29% of values showed less than ±10% difference while after normalization the number increased to 41%. Conclusions: Both methods correlate in an equal manner to FVIII:C in PWH but show a poor correlation with each other. The level of agreement for the TGA-CAT method was poor though slightly improved after normalization of data. Further improvement of standardization of these methods is warranted.
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    Does the intensity and quality of treatment and not only the factor VIII level influence global hemostasis in patients with hemophilia A?
    (2016)
    Berndtsson, Maria (6603376446)
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    Zetterberg, Eva (7801409763)
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    Holmström, Margareta (7006841518)
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    Mahmoud Hourani Soutari, Nida (57189844583)
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    Mikovic, Danijela (35585598700)
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    Elezovic, Ivo (12782840600)
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    Antovic, Jovan P. (6701874787)
    [No abstract available]
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    The Influence of Hyperthyroidism on the Coagulation and on the Risk of Thrombosis
    (2024)
    Antonijevic, Nebojsa (6602303948)
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    Matic, Dragan (25959220100)
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    Beleslin, Biljana (6701355427)
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    Mikovic, Danijela (35585598700)
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    Lekovic, Zaklina (58626922600)
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    Marjanovic, Marija (56437423000)
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    Uscumlic, Ana (56807174000)
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    Birovljev, Ljubica (58628000100)
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    Jakovljevic, Branko (8412749400)
    Introduction: Apart from the well-known fact that hyperthyroidism induces multiple prothrombotic disorders, there is no consensus in clinical practice as to the impact of hyperthyroidism on the risk of thrombosis. The aim of this study was to examine the various hemostatic and immunologic parameters in patients with hyperthyroidism. Methods: Our study consists of a total of 200 patients comprised of 64 hyperthyroid patients, 68 hypothyroid patients, and 68 euthyroid controls. Patient thyroid status was determined with standard tests. Detailed hemostatic parameters and cardiolipin antibodies of each patient were determined. Results: The values of factor VIII (FVIII), the Von Willebrand factor (vWF), fibrinogen, plasminogen activator inhibitor-1 (PAI-1), and anticardiolipin antibodies of the IgM class were significantly higher in the hyperthyroid patients than in the hypothyroid patients and euthyroid controls. The rate of thromboembolic manifestations was much higher in hyperthyroid patients (6.25%) than in hypo-thyroid patients (2.9%) and euthyroid controls (1.4%). Among hyperthyroid patients with an FVIII value of ≥1.50 U/mL, thrombosis was recorded in 8.3%, while in hyperthyroid patients with FVIII value ≤ 1.50 U/mL the occurrence of thrombosis was not recorded. The incidence of atrial fibrillation (AF) was significantly higher (8.3%) in the hyperthyroid patients compared to the hypothyroid patients (1.5%) and euthyroid controls (0%). Conclusions: High levels of FVIII, vWF, fibrinogen, PAI-1, and anticardiolipin antibodies along with other hemostatic factors contribute to the presence of a hypercoaguable state in patients with hyperthyroidism. The risk of occurrence of thrombotic complications is especially pronounced in patients with a level of FVIII exceeding 150% and positive anticardiolipin antibodies of the IgM class. Patients with AF are at particularly high risk of thrombotic complications due to a hyperthyroid prothrombotic milieu. © 2024 by the authors.
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    Two global haemostatic assays as additional tools to monitor treatment in cases of haemophilia A
    (2012)
    Antovic, Jovan P. (6701874787)
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    Mikovic, Danijela (35585598700)
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    Elezovic, Ivo (12782840600)
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    Holmström, Margareta (7006841518)
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    Wilkens, Matthias (49864844200)
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    Elfvinge, Petra (54789594700)
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    Soutari, Nida Mahmoud Hourani (55308888900)
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    Antovic, Aleksandra (6602938186)
    Haemophilia A patients with similar levels of factor VIII (FVIII) may have different bleeding phenotypes and responses to treatment with FVIII concentrate. Therefore, a test which determines overall haemostasis may be appropriate for treatment monitoring in some patients. We studied two global haemostatic methods: endogenous thrombin potential (ETP) and overall haemostatic potential (OHP) before and after injection of FVIII concentrate in patients with haemophilia A treated prophylactically and on-demand. A significant correlation between FVIII and both ETP and OHP was observed, while ETP and OHP differed between patients with severe and mild clinical phenotypes. Both ETP and OHP differed significantly between severe, moderate and mild haemophilia A and controls. ETP and OHP increased after intravenous injection of FVIII concentrate in both groups of patients, but in spite of higher pre-treatment values of both ETP and OHP in patients treated prophylactically, and much higher post-treatment FVIII levels in comparison with the values in patients treated on-demand, no difference after treatment was observed for either ETP or OHP. ETP and OHP may be additional alternatives for monitoring (and even for individual tailoring) treatment in patients with haemophilia A. © Schattauer 2012.

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