Arthur Nathaniel Billings ITP blood disorder health advices today? 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 blood disorder ITP 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.
You should avoid drugs like aspirin and non-steroidal anti-inflammatory drugs (e.g. ibuprofen, diclofenac) when your platelets are below 50 × 10^9/l because of a greater risk that gastric irritation could lead to bleeding. Also discuss any planned surgery or dental procedure with your haematologist (as well as informing the dentist or surgeon) so that a plan can be made. When to seek help If you have minor bleeding symptoms such as nose bleeds or bleeding in the mouth please ask your GP to carry out an urgent full blood count, or contact the haematology department. A purple rash called purpura (often on the lower legs) which does not fade when you press it may be a sign of a low platelet count.
The purple color of the skin after blood has “leaked” under it. A bruise is blood under the skin. Persons with ITP may have large bruises from no known injury. Bruises can appear at the joints of elbows and knees just from movement. Tiny red dots under the skin that are a result of very small bleeds. Nosebleeds, Bleeding in the mouth and/or in and around the gums, Heavy menstrual periods, Blood in the vomit, urine, or stool Bleeding in the head. This is the most dangerous symptom of ITP. Any head injury that occurs when there are not enough platelets to stop the bleeding can be life threatening. See more details at https://www.instagram.com/arthur.billings.351/.
Chronic thrombocytopenic purpura. The onset of the disorder can happen at any age, and the symptoms can last a minimum of 6 months, several years, or a lifetime. Adults have this form more often than children do, but it does affect adolescents. Females have it more often than males. Chronic ITP can recur often and requires continual follow-up care with a blood specialist (hematologist). What causes idiopathic thrombocytopenic purpura? In ITP, the immune system is stimulated to attack your body’s own platelets. Most often this is a result of antibody production against platelets. In a small number of cases, a type of white blood cell called T-cells will directly attack platelets. This immune system error may be a result of any of the following.