Browsing by Author "Thachil, Jecko (23029666900)"
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Publication Hemorrhage in acute promyelocytic leukemia—fibrinolysis in focus(2024) ;Sabljic, Nikica (57221634280) ;Thachil, Jecko (23029666900) ;Pantic, Nikola (57221630977)Mitrovic, Mirjana (54972086700)Coagulopathy continues to be a major challenge in the management of patients with acute promyelocytic leukemia (APL). Novel differentiating agents have led to improved survival in these patients, but perturbations in coagulation continue to have an impact on their prognosis. The most worrisome of coagulation disturbances is bleeding, which is not an uncommon cause of early death in APL. Despite this, there are no consistent predictors of this high risk of fatal hemorrhage in APL. In this context, the fibrinolytic system has been identified as a crucial role player in APL coagulopathy. However, the current guidelines for the management of APL give little regard to tests that measure the fibrinolytic system while giving more importance to close monitoring of conventional coagulation tests and platelet counts to identify the coagulopathy. More recently, viscoelastic tests have come to usefulness in determining global hemostasis and have been widely used for “diagnosing” hyperfibrinolysis in selected clinical settings. In this review, we attempt to describe risk assessment models for diagnosing APL coagulopathy, describe the possible application of viscoelastic tests in this setting, and persuade clinicians to reconsider the use of antifibrinolytics to improve survival of APL patients. © 2024 The Authors - Some of the metrics are blocked by yourconsent settings
Publication How do you decide on hormone replacement therapy in women with risk of venous thromboembolism?(2017) ;Lekovic, Danijela (36659562000) ;Miljic, Predrag (6604038486) ;Dmitrovic, Aleksandar (56341041400)Thachil, Jecko (23029666900)Women are increasingly encouraged to participate in making decisions about hormone replacement therapy (HRT). In postmenopausal women with severe vasomotor symptoms, HRT can significantly improve the quality of life. However, the use of HRT may also increase the risk of venous thromboembolism (VTE), the risk which depends of both treatment-related and patient-related factors. This review summarizes some important points about the selection of the safest hormonal replacement modality in women with a history of VTE and management of VTE risks in postmenopausal women wishing to take HRT. © 2016 Elsevier Ltd - Some of the metrics are blocked by yourconsent settings
Publication Platelet kinetics in patients with chronic immune thrombocytopaenia treated with thrombopoietin receptor agonists(2023) ;Pravdic, Zlatko (57221636770) ;Suvajdzic-Vukovic, Nada (36446767400) ;Djurdjevic, Predrag (7003269333) ;Pantic, Nikola (57221630977) ;Bukumiric, Zoran (36600111200) ;Virijevic, Marijana (36969618100) ;Todorovic-Tirnanic, Mila (12772684600) ;Thachil, Jecko (23029666900)Mitrovic, Mirjana (54972086700)Introduction: Thrombopoietin receptor agonists (TPO-RAs) increase platelet counts (PC) in the majority of patients with chronic immune thrombocytopaenia (ITP). Platelet kinetics study (PKS) might contribute to the understanding of mechanisms that lead to durable response. Objectives: To evaluate the effects of TPO-RAs on PKS parameters in chronic ITP patients. Methods: Fifteen chronic ITP patients, aged 59 years [range: 22–84], female/male: 10/5, splenectomised 7/15, were treated with TPO-RAs (eltrombopag/romiplostim: 11/4). Durable response was defined as PC ≥30 × 109/L at 6 months. Autologous 111Indium-oxinate PKS was performed before and 5 months after TPO-RAs initiation. Accordingly, platelet survival (PS), platelet turnover, production ratio and sequestration site were assessed. Results: Durable response was achieved in 13/15 of patients (eltrombopag/romiplostim: 10/3). Pre-treatment parameters were: PC 10 × 109/L [range: 1–110], PS 0.5 days [range: 0.1–1.7 (normal values: 7–10)], platelet turnover 30 857 Plt/μL/day [range: 944–103 500] and platelet production ratio 0.64 [range: 0.01–3.2 (normal values: 1 ± 0.2)]. Post-treatment assessment showed significantly higher: PC 92.5 × 109/L [range: 28–260, p =.001], PS 2.2 days [range: 0.1–3.6, p =.008], platelet turnover 70 213 Plt/μL/day [range: 2800–462 236, p =.02] and platelet production ratio 1.8 [range: 0.5–37.9, p =.011] compared to the pre-treatment values. Platelet sequestration site altered in 3/15 treated with TPO-RAs. Conclusions: TPO-RAs could increase PC by simultaneous increasing of platelet production and decreasing of platelet destruction. © 2023 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. - Some of the metrics are blocked by yourconsent settings
Publication Thrombosis in Acute Promyelocytic Leukemia: The Current Understanding(2023) ;Sabljic, Nikica (57221634280) ;Mitrovic, Mirjana (54972086700) ;Pantic, Nikola (57221630977)Thachil, Jecko (23029666900)Despite enormous improvement in the management of patients with acute promyelocytic leukemia (APL), the distinctive coagulopathy observed at presentation in affected patients is often life-threatening. While hemorrhagic manifestations are well known and described in this setting, APL-related thromboses are underappreciated. Data regarding this complication are scarce showing variable incidence. Furthermore, risk factors for thrombosis are inconsistent and unreliable; so, differentiation of increased risk of hemorrhage from an increased thrombotic risk is quite difficult in the absence of adequate predictive scores. Besides, prophylactic use of anticoagulants and recombinant thrombomodulin are a matter of ongoing debate. Also, due to the common feature of thrombocytopenia and other hemorrhagic risks, patients with APL are excluded from trials analyzing anticoagulant prophylaxis in cancers; so, data from prospective trials are lacking. A detailed analysis of thrombotic risks in APL with the development of a reliable risk stratification model is needed to further improve the care of APL patients. © 2024. Thieme. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Venous thromboembolism in patients with acute myeloid leukemia: development of a predictive model(2024) ;Mitrovic, Mirjana (54972086700) ;Pantic, Nikola (57221630977) ;Bukumiric, Zoran (36600111200) ;Sabljic, Nikica (57221634280) ;Virijevic, Marijana (36969618100) ;Pravdic, Zlatko (57221636770) ;Cvetkovic, Mirjana (58716866000) ;Ilic, Nikola (7006245465) ;Rajic, Jovan (57435044600) ;Todorovic-Balint, Milena (55773026600) ;Vidovic, Ana (6701313789) ;Suvajdzic-Vukovic, Nada (36446767400) ;Thachil, Jecko (23029666900)Antic, Darko (23979576100)Background: Patients with acute myeloid leukemia (AML) are at increased risk of venous thromboembolic events (VTE). However, thromboprophylaxis is largely underused. Objectives: This study aimed to determine possible VTE development risk factors and to develop a novel predictive model. Methods: We conducted a retrospective cohort study of adult patients with newly diagnosed AML. We used univariate and multivariable logistic regression to estimate binary outcomes and identify potential predictors. Based on our final model, a dynamic nomogram was constructed with the goal of facilitating VTE probability calculation. Results: Out of 626 eligible patients with AML, 72 (11.5%) developed VTE during 6 months of follow-up. Six parameters were independent predictors: male sex (odds ratio [OR] 1.82, 95% confidence interval [CI]: 1.077–2.065), prior history of thrombotic events (OR 2.27, 95% CI: 1.4–4.96), international normalized ratio (OR 0.21, 95% CI: 0.05–0.95), Eastern Cooperative Oncology Group performance status (OR 0.71, 95% CI: 0.53–0.94), and intensive therapy (OR 2.05, 95% CI: 1.07–3.91). The C statistics for the model was 0.68. The model was adequately calibrated and internally validated. The decision-curve analysis suggested the use of thromboprophylaxis in patients with VTE risks between 8 and 20%. Conclusion: We developed a novel and convenient tool that may assist clinicians in identifying patients whose VTE risk is high enough to warrant thromboprophylaxis. © The Author(s) 2024.
