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- W4384401101 abstract "Abstract Objectives This study aimed to describe the burden of thrombocytopenia, supportive care practices, bleeding complications and predictors of bleeding in MDS patients within a large Australian hospital network, to better understand the use and effectiveness of platelet transfusions in MDS. Methods A retrospective cohort study of patients aged ≥18 years with MDS, chronic myelomonocytic leukaemia or MDS/myeloproliferative overlap neoplasm admitted from 2016 to 2018 was conducted. Data were obtained from hospital medical records. Results One hundred seventy‐nine patients (median age 78 years, 61.5% male) were identified. The median platelet count at first admission was 90 × 10 9 /L. Twenty‐eight (15.6%) patients had severe thrombocytopenia (platelet count <20 × 10 9 /L), of whom nine (32.1%) received prophylactic platelet transfusions, five (17.9%) received tranexamic acid (TXA), seven (25%) received both platelet transfusions and TXA, and seven (25%) received no treatment. Bleeding events requiring hospitalisation occurred in 20 (11.2%) patients. Bleeding was not predicted by presenting platelet count, TXA use, platelet transfusion or anticoagulant/antiplatelet therapies. Three patients died of bleeding, at varying platelet counts (18, 38 and 153 × 10 9 /L). Conclusion Thrombocytopenia is common in MDS. Although guidelines recommend otherwise, prophylactic platelet transfusions were commonly used for severe thrombocytopenia. Despite the majority of patients receiving platelet transfusions and/or TXA, 11% developed major bleeding occurring at a wide range of platelet counts." @default.
- W4384401101 created "2023-07-16" @default.
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- W4384401101 date "2023-07-15" @default.
- W4384401101 modified "2023-10-17" @default.
- W4384401101 title "Platelet transfusions and predictors of bleeding in patients with myelodysplastic syndromes" @default.
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- W4384401101 doi "https://doi.org/10.1111/ejh.14049" @default.
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