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Sickle Cell Anemia
- Overview, Causes, & Risk Factors
- Symptoms & Signs
- Diagnosis & Tests
- Prevention & Expectations
- Treatment & Monitoring
- Attribution
Overview, Causes, & Risk Factors
Sickle cell anemia is an inherited blood disease. It causes serious health problems among African Americans or individuals of African descent.
What is going on in the body?
Hemoglobin is the key molecule in the blood that carries oxygen to all parts of the body. A change in a certain gene causes a change in the structure of hemoglobin. Persons with normal hemoglobin have a genetic coding of AA. Persons with sickle cell trait have a genetic coding of AS. (The "S" refers to the sickle cell gene.)
Eight percent of African Americans are carriers of the sickle cell gene, and are said to have sickle cell trait. Most people with sickle cell trait are completely healthy and lead normal lives. Persons with the genetic coding SS have a double dose of the abnormal hemoglobin gene. They develop sickle cell anemia. It affects approximately 15 out of every 1000 African Americans.
In sickle cell anemia the red blood cells change shape from a rounded disk to a crescent or "sickle" shape. These abnormal red blood cells are more rigid and are more likely to clump together. They are also more likely to stick to the walls of blood vessels. They can even block the blood vessels themselves. These changes also mean that the hemoglobin molecule isn't able to carry oxygen as well as it should.
What are the causes and risks of the disease?
Sickle cell anemia is caused by a change in a gene that changes the structure of the hemoglobin molecule.
Sickle cell anemia is a long-term disease that causes a number of health risks. Individuals have a severe anemia that puts extra strain on the heart, which can lead to heart enlargement. These individuals have a reduced life expectancy. They are at increased risk of the following:
Pregnant women with sickle cell anemia are likely to have kidney infections, bleeding, premature infants, and fetal death.
Symptoms & Signs
What are the signs and symptoms of the disease?
Persons with sickle cell anemia have many symptoms. They often have problems in growth and development. Individuals may have pain in the joints and chest pain that is worse when they take a deep breath. Sickle cell anemia causes repeated bouts of severe pain. These are called "painful crises" or "thrombotic crises." These attacks of pain are sudden, severe, and affect many areas of the body. The most common areas are the arms, legs, abdomen, chest, and back. The pain can last hours to several days or even weeks. During these painful crises there may be a high fever. The person may require hospitalization. There is no specific cure for the episodes.
The signs of sickle cell anemia can include:
Diagnosis & Tests
How is the disease diagnosed?
The disease is diagnosed through a combination of medical history, physical examination, and laboratory testing. A vital laboratory test is the peripheral blood smear. This test will show the characteristic sickle shape of some red blood cells. There is usually a very low red blood cell count. This is due to the breakdown of the red blood cells. White blood cells counts are often higher than normal. Liver function tests may be abnormal. A specialized test called hemoglobin electrophoresis will confirm the diagnosis. X-rays may show abnormal changes in bone, especially of the spine and hip.
Prevention & Expectations
What can be done to prevent the disease?
For an individual with the SS genetic coding for hemoglobin, there is no effective prevention of sickle cell anemia. However, individuals with sickle cell trait (AS coding) can benefit from genetic counseling. If two parents are both carriers of the sickle cell trait, they have a 25% chance of having a child with sickle cell anemia.
What are the long-term effects of the disease?
Many individuals with sickle cell anemia develop serious, long-term medical problems. These include:
The repeated episodes of severe pain often reduce the quality of daily life. Narcotic pain relievers are often used to treat these painful crises. This can lead to a risk of becoming dependent on these drugs.
What are the risks to others?
Sickle cell anemia is passed from parent to child. It is not contagious.
Treatment & Monitoring
What are the treatments for the disease?
Sickle cell anemia is a lifelong chronic disease. There is no cure. Because sickle cell anemia causes so many health problems, persons with the disease need to establish a good relationship with a doctor.
Some treatments for sickle cell anemia help to prevent other complications.
What are the side effects of the treatments?
General supportive care, such as pain control and fluids, has no specific side effects.
What happens after treatment for the disease?
After treatment of a specific problem, such as a painful crisis or an infection, the person may have periods of time with few symptoms.
How is the disease monitored?
There is no specific test for monitoring sickle cell anemia. A person's symptoms and certain lab tests are the best ways to monitor the disease.
Attribution
Author:Minot Cleveland, MD
Date Written:
Editor:Smith, Mary Ellen, BS
Edit Date:03/20/00
Reviewer:Sandy Keefe, RN, MSN
Date Reviewed:09/20/01