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Sickle Cell Anemia

Red blood cells are normally round. In sickle cell anemia, the red blood cells take on a sickle shape. This makes the blood thicker and doesn’t let oxygen get to the body’s tissues like it should. When sickled cells get stuck in the blood vessels, they cut off the blood supply. With no oxygen, pain occurs. The result is a “Sickle Cell Crisis.”

Signs &

Symptoms

Causes

Treatment

Questions
to Ask

Self-Care /

Prevention

•  Bone and joint pain. This is the most common complaint. The pain can also be in the chest, back, or abdomen.

•  Shortness of breath and a hard time breathing.

•  Swollen hands and feet.

•  Jaundice. The whites of the eyes and/or the skin looks yellow.

•  Paleness.

•  Repeated infections, especially pneumonia or meningitis.

•  Kidney problems. Leg ulcers. Gallstones (at an early age). Gout.

•  Seizures.

•  Strokes (at an early age).

Illustration of sickle cell anemia.

Sickle cell anemia is inherited. In the U.S., it mostly affects African Americans, but can occur in other ethnic groups. Examples are persons whose ancestors are from Cuba, Central and South America, Greece, Italy, Turkey, and Saudi Arabia. About 1 in 12 African Americans carries the gene for the sickle cell trait. If both parents carry the trait, the chance of having a child with sickle cell anemia is 1 out of 4. About 1 in 375 African Americans and about 1 in every 1,000 Latin Americans are born with sickle cell anemia. Signs of the disease aren’t noticed until the end of the infant’s first year. All hospitals in the U.S. screen newborns for sickle cell disease.

 

To prevent sickle cell anemia in offspring, couples, especially African American couples, should have a blood test to see if they are carriers for the sickle cell trait. Genetic counseling can help them decide what to do.

Illustration of sickle cell anemia.

Medical treatment is needed. Painful episodes are treated with painkillers, fluids, and oxygen. Other treatments:

•  Hydroxyurea medicine.

•  Blood transfusions.

•  Stem cell transplant. This may be an option for children who have a brother or sister without sickle cell disease that is a matched donor.

In the U.S., the life span for a person with sickle cell disease is 40-60 years.

Image of needles and treatment.
Image of smiling doctor.

•  Follow your doctor’s treatment plan. Wear a medical alert tag.

•  Avoid physical stress and high altitudes.

•  Discuss airplane travel with your doctor.

•  Ask your doctor what over-the- counter medicines you can use before you try any.

•  Drink at least 8 glasses of water a day. Get the rest you need.

•  Follow a balanced diet. Have at least 5 servings of fruits and vegetables a day. Take folic acid (a B vitamin) supplements and other vitamins and minerals, as advised by your doctor.

•  Don’t wear tight clothing.

•  If at home and in a “sickle cell crisis:”

– Stay warm. Apply warm compresses to painful parts of your body.

– Rest in bed.

– Take pain medication, as prescribed.

This website is not meant to substitute for expert medical advice or treatment. Follow your doctor’s or health care provider’s advice if it differs from what is given in this guide.

 

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