Treatment strategies for Immune Thrombocytopenia (ITP) are personalized based on the severity of the disease, the risk of bleeding, and individual patient characteristics. First-line therapies generally include corticosteroids and intravenous immunoglobulin (IVIG), which help to reduce the immune-mediated destruction of platelets. For individuals with chronic or refractory ITP, second-line treatments may involve thrombopoietin receptor agonists, monoclonal antibodies, or even splenectomy.