What should I eat if I have low platelets? I used to take cyclosporine and Stanozolol, and my platelet count was always in the single digits. I would turn blue when I touched something strong, my face would be pale and weak, and I would be out of breath and sweating when I moved. Later, I used the method mentioned in "Yu Qihua's Tortuous Treatment Experience" After taking the decoction for a period of time, not only did the discomfort symptoms improve very well, but the platelet count also improved very well from single digits to over 20 to over 50 and over 80. After persisting for about half a year, the platelet returned to normal.
Platelets are destroyed or consumed too much. ① Congenital: including non-immune diseases, such as hemolytic disease of the newborn, thrombocytopenia of prematurity, neonatal infections, etc.; immune diseases, such as neonatal alloimmune thrombocytopenia, neonatal essential thrombocytopenia, Neonatal drug-induced thrombocytopenia, etc. ② Acquired: non-immune diseases, such as viral infections (influenza, rubella, epidemic hemorrhagic fever), bacterial infections (sepsis, subacute bacterial endocarditis), protozoal infections (toxoplasmosis), thrombotic thrombocytopenia Purpura, hemolytic uraemia, disseminated intravascular coagulation, pregnancy, etc. can all cause it; immune diseases, such as drug-induced immune thrombocytopenia, post-transfusion purpura, and idiopathic thrombocytopenic purpura.
Decreased platelet production. ① Hereditary thrombocytopenia: such as radial ischemia with thrombocytopenia, congenital amegakaryocytic thrombocytopenia, thrombopoietin deficiency, bone marrow infiltrative diseases (congenital leukemia, malignant histiocytosis) and neonatal rubella, etc. . ②Acquired thrombocytopenia: aplastic anemia, simple megakaryocytic aplasia thrombocytopenia, tumor cell infiltration into bone marrow, myelosclerosis, physical effects (such as radiation), chemical factors (such as drugs), cyclic thrombocytopenia, bacteria Infection, nutritional deficiencies, alcohol consumption and hemolysis.
Abnormal platelet distribution or excessive retention in the spleen. Splenomegaly caused by liver cirrhosis, schistosomiasis, splenic lymphoma, cavernous sinusoid hemangioma, myelofibrosis, etc., leads to excessive platelet retention in the spleen and causes peripheral blood thrombocytopenia.