| Sumario: | Immune thrombocytopenia purpura (ITP), also known as idiopathic thrombocytopenic purpura, is an autoimmune disorder characterised by reduced platelets in the blood. Platelets are vital for blood clotting and help to prevent excessive bleeding. When platelet levels drop, it can result in symptoms such as bruising, bleeding gums, petechial rashes, and, in severe cases, internal bleeding. This reduction occurs because the body's immune system mistakenly attacks its platelets. This article provides an overview of the latest guidelines for diagnosing and managing ITP, including a discussion of newly approved treatments. Clinical nurse specialists and advanced nurse practitioners are crucial in guiding patients through treatment, helping manage side-effects, and offering support to patients and their families.
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