Definition and diagnosis of immune thrombocytopenic purpura ITP is defined as isolated thrombocytopenia with no clinically apparent associated conditions or other causes of thrombocytopenia. 3 This definition provides the basis for the initial patient evaluation.
of patients with suspected ITP, assuming that the history, physical examination, and blood counts are compatible with the diagnosis of ITP and do not include atypical findings that are uncommon in ITP or suggest other etiologies. Pa- tients with risk factors for HIV infection should be tested for HIV antibody.
Primary immune thrombocytopenia (ITP, also called idiopathic thrombocytopenic purpura, immune thrombocytopenic purpura) is an acquired thrombocytopenia caused by autoantibodies against platelet antigens. It is one of the more common causes of thrombocytopenia in otherwise asymptomatic adults.
Diagnosis. To diagnose idiopathic thrombocytopenic purpura, your doctor will try to exclude other possible causes of bleeding and a low platelet count, such as an underlying illness or medications you or your child may be taking.
We proposed diagnostic criteria for immune thrombocytopenic purpura (ITP) by modifying the existing guidelines for diagnosis of ITP and by incorporating laboratory tests found useful for predicting its diagnosis, for example erythrocyte count, leukocyte count, anti-GPIIb/IIIa antibody-producing B
immune thrombocytopenic purpura, idiopathic thrombocytopenic purpura, idiopathic immune thrombocytopenia, primary immune thrombocytopenia, idiopathic thrombocytopenic purpura, primary immune thrombocytopenic purpura, autoimmune thrombocytopenic purpura It is recommended that pregnant women with thrombocytopenia or a previous diagnosis …
Hear from real patients about their experiences with chronic idiopathic thrombocytopenia (ITP) and see how each one reacted to his or her diagnosis.
ITP, Immune Thrombocytopenic Purpura, is an acquired bleeding disorder in which the immune system destroys platelets, blood cells that play a …
Apr 23, 2018 · Immune thrombocytopenic purpura (ITP)—also known as idiopathic thrombocytopenic purpura and, more recently, as immune thrombocytopenia—is a clinical syndrome in which a decreased number of circulating platelets (thrombocytopenia) manifests as a bleeding tendency, easy bruising (purpura), or …
Medical criteria, definitions, indications, contraindications, classifications, diagnosis. Heparin exposure >5 days; Relative thrombocytopenia: decrease in platelet count by 50% from baseline OR absolute thrombocytopenia: decrease in platelet count to less than 100 to 150 x 10 9 /L; Absence of other causes of thrombocytopenia