Journals / Acta Medica / 2019 / Cilt: 50 - Sayı: 2

Thrombosis and Bleeding in Philadelphia Negative Myeloproliferative Neoplasia: Incidences and Risk Factors

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1–7
DOI
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⚡ TL;DR(Too Long; Didn't Read)

Further experimental and clinical studies should focus on the pathobiology and proper clinical management of the myeloproliferative neo-plasm patients with hemostatic complications.

📌 3 Key Takeaways

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Objective & Hypothesis:Objective: Thrombohemorrhagic events developing in the Philadelphia neg-ative myeloproliferative neoplasms may worsen the clinical course of the dis-ease and increase the morbidity and mortality.
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Key Findings & Data:The aim of this study is to as-sess critical risk factors of the hemostatic complications in myeloprolifera-tive neoplasms.Materials and Methods: The patients who were diagnosed as myeloprolif-erative neoplasm based on world health organization 2016 criteria are in-cluded into the study.
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Conclusion & Impact:Further experimental and clinical studies should focus on the pathobiology and proper clinical management of the myeloproliferative neo-plasm patients with hemostatic complications.
🔬Design:Research Article
📍Scope:2016 Verileri
⚙️Variables:Domain Parameters

Özet

Objective: Thrombohemorrhagic events developing in the Philadelphia neg-ative myeloproliferative neoplasms may worsen the clinical course of the dis-ease and increase the morbidity and mortality. The aim of this study is to as-sess critical risk factors of the hemostatic complications in myeloprolifera-tive neoplasms.Materials and Methods: The patients who were diagnosed as myeloprolif-erative neoplasm based on world health organization 2016 criteria are in-cluded into the study. The categorical and continuous data were compared with Chi-square and independent sample t-test. The statistical significance threshold was considered as p <0.05.Results: 181 patients were evaluated in this study. The number of the pa-tients with polycythemia vera, essential thrombocytosis and primary myelo-fibrosis were 89, 50 and 42 respectively. At the time of diagnosis, the median age was 54 years. There were 50 patients who had thrombosis at the time of diagnosis, and 22 patients have developed thrombosis during the follow-up. Venous thrombosis is more frequent than arterial thrombosis. The smoking habit was statistically higher in the patient with myeloproliferative neoplasm who developed thrombosis (p=0.006). The most frequent hemorrhagic com-plication was gastrointestinal bleeding. Platelet levels of patients with com-plications during the course of myeloproliferative neoplasm were found to be lower than those without complications (p <0.001).Conclusion: The hemostatic complication rates due to myeloproliferative neoplasm were 39% thrombosis and 13% bleeding. While the cigarette us-age was significantly higher in the thrombosis group, advanced age, male sex, types of myeloproliferative neoplasm, JAK-2 positivity were similar between the groups. Further experimental and clinical studies should focus on the pathobiology and proper clinical management of the myeloproliferative neo-plasm patients with hemostatic complications.

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Cite This Article

OKAY, M., MALKAN, Ü. Y., BÖLEK, E. Ç., SAYINALP, N., BÜYÜKAŞIK, Y., HAZNEDAROĞLU, İ. (2019). Thrombosis and Bleeding in Philadelphia Negative Myeloproliferative Neoplasia: Incidences and Risk Factors. Acta Medica, Cilt: 50 - Sayı: 2, 1–7. https://ajindex.com/articles/141984

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References (9)

  1. Martin K. Risk Factors for and Management of MPN-Associated Bleeding and Thrombosis. Current hemato-logic malignancy reports 2017;12:5389-96.
  2. Baş B, Köksal A, Özatll D, Haznedaroglu I, Koşar A, Büyükaşik Y, Ozcebe O, Dündar S. Thrombosis and hemor-rhage in chronic myeloproliferative disorders. Clinical and Applied Thrombosis/Hemostasis 1999;5:4282-4.
  3. Kaifie A, Kirschner M, Wolf D, Maintz C, Hänel M, Gattermann N, Gökkurt E, Platzbecker U, Hollburg W, Göthert J. Bleeding, thrombosis, and anticoagulation in myeloproliferative neoplasms (MPN): analysis from the German SAL-MPN-registry. Journal of hematology & on-cology 2016;9:118. Norris D, Stone J. WHO classification of tumours of haema-topoietic and lymphoid tissues. Geneva: WHO 2008.
  4. Papadakis E, Hoffman R, Brenner B. Thrombohemorrhagic complications of myeloproliferative disorders. Blood re-views 2010;24:6227-32.
  5. Finazzi G, Carobbio A, Thiele J, Passamonti F, Rumi E, Ruggeri M, Rodeghiero F, Randi ML, Bertozzi I, Vannucchi AM. Incidence and risk factors for bleeding in 1104 pa-tients with essential thrombocythemia or prefibrotic my-elofibrosis diagnosed according to the 2008 WHO criteria. Leukemia 2012;26:4716. Wehmeier A, Daum I, Jamin H, Schneider W. Incidence and clinical risk factors for bleeding and thrombotic complica-tions in myeloproliferative disorders. Annals of hematolo-g y 19 91; 63:2101- 6. Carobbio A, Thiele J, Passamonti F, Rumi E, Ruggeri M, Rodeghiero F, Randi ML, Bertozzi I, Vannucchi AM, Antonioli E. Risk factors for arterial and venous thrombosis in WHO-defined essential thrombocythemia: an international study of 891 patients. Blood 2011:blood-2011-02-339002.
  6. Barbui T, Finazzi G, Carobbio A, Thiele J, Passamonti F, Rumi E, Ruggeri M, Rodeghiero F, Randi ML, Bertozzi I. Development and validation of an International Prognostic Score of thrombosis in WHO-Essential Thrombocythemia (IPSET-thrombosis). Blood 2012:blood-2012-07-444067.
  7. Ruggeri M, Rodeghiero F, Tosetto A, Castaman G, Scognamiglio F, Finazzi G, Delaini F, Mico C, Vannucchi AM, Antonioli E. Postsurgery outcomes in patients with polycythemia vera and essential thrombocythemia: a ret-rospective survey. Blood 2008;111:2666-71.
  8. Gangat N, Wolanskyj AP, Schwager SM, Mesa RA, Tefferi A. Estrogen‐based hormone therapy and thrombosis risk in women with essential thrombocythemia. Cancer 2006;106:112406-11.
  9. De Stefano V, Za T, Rossi E, Fiorini A, Ciminello A, Luzzi C, Chiusolo P, Sica S, Leone G. Influence of the JAK2 V617F mutation and