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Sickle cell anemiaDefinition Sickle cell anemia is an inherited disease in which the red blood cells, normally disc-shaped, become crescent shaped. As a result, they function abnormally and cause small blood clots. These clots give rise to recurrent painful episodes called "sickle cell pain crises." Causes, incidence, and risk factors Sickle cell anemia is caused by an abnormal type of hemoglobin called hemoglobin S. Hemoglobin is a protein inside red blood cells that carries oxygen. Hemoglobin S, however, reduces the amount of oxygen inside the cells, distoring their shape. The fragile, sickle-shaped cells deliver less oxygen to the body's tissues, and can break into pieces that disrupt blood flow. Sickle cell anemia is inherited as an autosomal recessive trait , which means it occurs in someone who has inherited hemoglobin S from both parents. Sickle cell disease is much more common in certain ethnic groups, affecting approximately one out of every 500 African Americans. Someone who inherits hemoglobin S from one parent and normal hemoglobin (A) from the other parent will have sickle cell trait. Someone who inherits hemoglobin S from one parent and another type of abnormal hemoglobin from the other parent will have another form of sickle cell disease, such as thalassemia. Although sickle cell disease is present at birth, symptoms usually don't occur until after 4 months of age. Sickle cell anemia may become life threatening . Blocked blood vessels and damaged organs can cause acute painful episodes, or "crises." There are several types of crises:
These painful crises, which occur in almost all patients at some point in their lives, can last hours to days, affecting the bones of the back, the long bones, and the chest. Some patients have one episode every few years, while others have many episodes per year. The crises can be severe enough to require admission to the hospital for pain control and intravenous fluids. Repeated crises can cause damage to the kidneys, lungs, bones, eyes, and central nervous system. Symptoms Common symptoms include:
The patient may also have:
Signs and tests Tests commonly performed to diagnose and monitor patients with sickle cell anemia include:
Patients with sickle cell may have abnormal results on certain tests, as follows:
Treatment Patients with sickle cell disease need continous treatment, even when they are not having a painful crisis. Supplementation with folic acid, an essential element in producing cells, is required because of the rapid red blood cell turnover. The purpose of therapy is to manage and control symptoms and to try to limit the frequency of crises. During a sickle crisis, certain therapies may be necessary. Painful episodes are treated with analgesics and adequate liquid intake. Treatment of pain is critical. Non-narcotic medications may be effective, but some patients will require narcotics. Hydroxyurea (Hydrea) was found to help some patients by reducing the frequency of painful crises and episodes of acute chest syndrome and decreasing the need for blood transfusions. There has been some concern about the possibility of this drug causing leukemia, but as yet there are no definitive data that Hydrea causes leukemia in sickle cell patients. Newer drugs are being developed to manage sickle cell anemia. Some of these agents work by trying to induce the body to produce more fetal hemoglobin (therefore decreasing the amount of sickling) or by increasing the binding of oxygen to sickle cells. But as yet, there are no other widely used drugs that are available for treatment. Bone marrow transplants can be curative, this therapy is indicated in only a minority of patients, predominantly because of the high risk of the procedure (the drugs needed to make the transplant possible are highly toxic) and difficulty in finding suitable donors. Also, bone marrow transplants are much more expensive than other treatments. Antibiotics and vaccines are given to prevent bacteria infections, which are common in children with sickle cell disease. Additional treatments may include:
Support Groups Sickle cell anemia, like other chronic, life-threatening diseases, can causegreat stress to the patient and family members. Joining a support group, wheremembers share common experiences and problems, can relieve this stress. Seesickle cell anemia - support group. Expectations (prognosis) In the past, death from organ failure often occurred between the ages of 20 and 40 in most sickle-cell patients. More recently, because of better understanding and management of the disease, patients live into their forties and fifties. Causes of death include organ failure and infection. Some people with the disease experience minor, brief, and infrequent episodes. Others experience severe, prolonged, and frequent episodes resulting in many complications. Complications
Calling your health care provider Call your health care provider if acute painful crises occur or at the first sign of any infection. Prevention Sickle cell anemia can only result when two carriers with sickle cell trait have a child together. Therefore, genetic counseling is recommended for all carriers of sickle cell trait (about 1 in 12 African Americans has sickle cell trait ). Prenatal diagnosis of sickle cell anemia is also available. Prompt treatment of infections, adequate oxygenation, and preventing dehydration may prevent sickling of red blood cells. Antibiotics and vaccinations may prevent infections. General health visits with a physician are recommended to ensure the patient is getting adequate nutrition, maintaining proper activity levels, and receiving proper vaccinations. PREVENTING CRISES Parents whose children have sickle cell should encourage their children to lead normal lives. However, in order to decrease the occurrence of sickle cell crises, consider the following precautions: To prevent tissue deoxygenation, avoid the following:
To promote proper hydration:
To avoid sources of infection:
Illustrations
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