Bleeding disorders are miserable conditions that disturb a number of people around the world. Hemophilia harms nearly 20,000 people in the United States and more than 400 children are born each year with this disease. Several cases of hemophilia occur almost especially in men; women can still have cell that can fight with the hemophilia, but only develop mild forms of the bleeding disorder. There are some more Other forms of this disorders which include: 1. Acquired platelet function defects 2. Congenital platelet function defects 3. Congenital antithrombin III deficiency 4. Congenital protein C or S deficiency 5. Disseminated intravascular coagulation (DIC) 6. Drug-induced immune thrombocytopenia 7. Factor II deficiency 8. Factor V deficiency 9. Factor VII deficiency Bleeding disorders can result from a number of different reasons and can be either inherited or gained. The most common aspect of these disorders is a lack of the blood parts responsible for clotting which is known as platelets. The result is excessive or continuous bleeding that takes longer for the body to control or not normal. Blood Transfusions as Treatment for Hemophilia During the first half of the 20th century, it was very common among hemophilia patients and patients with other kind of clotting disorders to be treated with “blood transfusions”. The process initially involved the transfusion of whole blood or frozen plasma. This was a laborious process, requiring extended hospital stays for each treatment. In the 1970s and 80s, the specific clotting factors in the blood became available in more adaptable, concentrated forms. Since the clotting factors were the only parts of the blood that hemophiliacs and other patients with bleeding disorders required from the whole blood or plasma, blood transfusions were no longer essential. Unfortunately, whether attained from “blood transfusions” or through concentrated plasma extracts, the needed platelets still had to come from donor blood banks. By 1987, it became clear-cut that an alarming number of hemophiliac and other bleeding disorder patients had become influence with hepatitis B, hepatitis C, and HIV (the virus that causes AIDS) due to contaminated donor blood. Although major stomp have been made since the late 1980s to improve the security of donor blood, there are still a number of danger associated with receiving donated blood parts through blood transfusions or other any available methods. Patients suffering from hemophilia and other bleeding disorders are at risk for any blood borne pathogen, allergic reactions and a number of other complications that can result from receiving donor blood parts or the transfusion process itself. So be aware when you have to come across the blood taking procedure.
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