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Condition

Idiopathic Thrombocytopenic Purpura

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Condition 101

What is the definition of Idiopathic Thrombocytopenic Purpura?

Idiopathic thrombocytopenic purpura (ITP) is a bleeding disorder characterized by too few platelets in the blood. This is because platelets are being destroyed by the immune system. Symptoms may include bruising, nosebleed or bleeding in the mouth, bleeding into the skin, and abnormally heavy menstruation. With treatment, the chance of remission (a symptom-free period) is good. Rarely, ITP may become a chronic ailment in adults and reappear, even after remission.

What are the alternative names for Idiopathic Thrombocytopenic Purpura?

  • ITP
  • Autoimmune thrombocytopenic purpura
  • Thrombocytopenic purpura autoimmune

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Latest Research

Latest Advance
Study
  • Condition: Primary Immune Thrombocytopenia (ITP)
  • Journal: Annals of hematology
  • Treatment Used: Steroids, Splenectomy, Rituximab, and Eltrombopag
  • Number of Patients: 175
  • Published —
This study investigated the outcomes, response to treatment, and predictors of chronicity in patients with primary immune thrombocytopenia (ITP).
Latest Advance
Study
  • Condition: Immune Thrombocytopenia
  • Journal: The Lancet. Haematology
  • Treatment Used: Eltrombopag Versus Intravenous Immunoglobulin
  • Number of Patients: 74
  • Published —
In this study, researchers compared the effectiveness of eltrombopag versus intravenous immunoglobulin for the treatment of immune thrombocytopenia.