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- W4245646343 abstract "Immune thrombocytopenia (ITP) is a disease caused by autoimmune platelet destruction that can occur as a primary or secondary process. ITP is a diagnosis of exclusion with no confirmatory diagnostic test. Diagnostic bone marrow biopsy should be pursued in select cases: abnormalities on peripheral smear, abnormal white blood cell count or hemoglobin, or treatment-refractory ITP. Treatment for ITP should be initiated in patients with less than 30,000 platelets per microliter or significant bleeding. First-line treatment for primary ITP is high-dose dexamethasone , intravenous immunoglobulin, or anti-D immunoglobulin. Splenectomy should be deferred for at least 6 months in favor of treatments with lower morbidity." @default.
- W4245646343 created "2022-05-12" @default.
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- W4245646343 date "2017-01-01" @default.
- W4245646343 modified "2023-09-25" @default.
- W4245646343 title "Immune Thrombocytopenia" @default.
- W4245646343 doi "https://doi.org/10.1016/j.ehmc.2016.07.005" @default.
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