Autoimmune thrombocytopenic purpura can be divided into childhood immune thrombocytopenic purpura and adult immune thrombocytopenic purpura, of which childhood immune thrombocytopenic purpura is mostly acute and most of them can be cured, whereas adult immune thrombocytopenic purpura is mostly chronic and cannot be completely cured, but the symptoms can be effectively improved after active treatment.
1. Children’s immune thrombocytopenic purpura: children’s immune thrombocytopenic purpura often has a history of viral infection, usually starts suddenly, often within a few hours of the attack, after active treatment, most patients can be cured, but there are a small number of patients will be converted to chronic thrombocytopenic purpura. Drugs include prednisone, immunoglobulin and so on.
2. Adult immune thrombocytopenic purpura: Adult immune thrombocytopenic purpura usually has an insidious onset, often manifested as skin bleeding, ecchymosis, and the progression of the disease can usually be controlled by treatment, but it may still be recurrent and prolonged. The medication is the same as above.
It is recommended that patients go to the hospital as soon as possible, and actively cooperate with the doctor’s treatment to prevent the development of the disease, affecting the therapeutic effect.