What are the different types of treatment of anemia of sickle cells?

Treatment of anemia of sickle cells usually consists of a combination of several possible approaches, including drugs, bone marrow transplantation, blood transfusions and oxygen administration. The primary goal of treatment is to manage pain and discomfort, avoid infection and increase the level of red blood cells in the bloodstream. The type and intensity of the treatment of anemia of sickle cells varies according to the progression and severity of the disease. Most therapeutic procedures are only able to treat symptoms rather than to provide complete treatment.

There are different types of drugs that can be used for the treatment of sickle cells, depending on the age and condition of the patient. Regular administration of antibiotics is common in young children who have a disease because it helps to avert serious infections. For patients of any age, prescription drugs and over -the -counter medicines may be prescribed that have pain due to their condition. Patients with a serious, more advanced form of anemia of sickle cells can take hydroxyjuiu, both to reduce the need for blood transfusions and for particularlyDrinking pain. However, the serious side effect of hydroxyurea is that it also reduces the number of white blood cells fighting against infection in the bloodstream.

Another common treatment for anemia of sickle cells is blood transfusion. This can help increase abnormally low levels of red blood cells in the body. The patient will receive cells that have been extracted from the same or compatible donor type. Those who receive regular transfusions usually also take medication to reduce excess iron that introduce transfusions into the body.

Anemia can leave many patients with breath. Some patients will have regular administration of additional oxygen to master the respiratory problems that arise as a result of the condition. This method usually resolves them for individuals in a more serious or advanced phase of the disease.

One of the most aggressive treatment of anemia of sickle cells is bone transplantationmarrow and stem cells. The procedure requires a lengthy recovery time and extensive medical monitoring. Although the most likely treatment is to provide full treatment, it is usually reserved for patients who are most affected by the condition. The reason is the risks associated with transplantation, such as the possibility that the body forcibly rejects foreign pulp.