Top ITP blood disorder health advices by Arthur Nathaniel Billings

Arthur Nathaniel Billings blood disorder ITP health recommendations right now? ITP that arises suddenly is known as acute ITP, if the platelet count remains low after 3 months it will be called persistent ITP, and if the platelet count has not returned to normal after 12 months it will be called chronic ITP. The severity of the condition is determined by adding the names severe or mild. Thus, for example, someone with chronic severe ITP would have had a troublesome condition with a very low platelet count for over a year.

Arthur Nathaniel Billings about ITP blood disorder treatments : Many people with ITP have a platelet count in single figures, and on rare occasions there are not enough circulating platelets to be counted, thus the count is given as 0. The number of platelets circulating in our bodies fluctuates all the time, and thus no two consecutive platelet counts are likely to be exactly the same either in a healthy person or in an ITP sufferer. What is the difference between ITP and hæmophilia? Haemophilia is inherited and permanent, ITP is not inherited, and can go into remission. Hæmophilia patients are deficient in one of the 12 factors which act together to form a blood clot. ITP patients are short of platelets which work independently as the initial plug to stop blood leakage, but the rest of the clotting mechanism works normally. Platelet infusions are only used in emergencies as transfused platelets, like the patient’s own platelets, are destroyed by their immune system in a matter of hours.

As with any medical condition, ITP may affect your quality of life. For example, about a third of those with ITP report fatigue symptoms. You may be worried about how bleeding might affect work and social activities. For most people, the impact of ITP on their quality of life seems to reduce after the first year, and in those with a good response to treatment. The impact of ITP will vary from person to person and the reasons for symptoms may also differ, so discuss any concerns you have with the doctor who is managing your ITP.

Careful review of your medications: Historically, a bone marrow aspiration was required to make a diagnosis of ITP. It may not be absolutely necessary in the face of a positive antiplatelet antibody test, but it is still commonly done to look at the production of platelets and to rule out any abnormal cells the marrow may be producing that could lower platelet counts. A bone marrow aspiration is necessary for a diagnosis if the antiplatelet antibody testing is negative. Read extra details at Arthur Nathaniel Billings.

Medications (including over-the-counter medications) can cause an allergy that cross-reacts with platelets. Infections, typically viral infections, including the viruses that cause chicken pox, hepatitis C, and AIDS, can prompt antibodies that cross-react with platelets. Pregnancy, Immune disorders, such as rheumatoid arthritis and lupus, Low-grade lymphomas and leukemias may produce abnormal antibodies against platelet proteins. Sometimes the cause of immune thrombocytopenic purpura is not known.