A blood test can check for the form of hemoglobin that underlies sickle cell anemia. In the United States, this blood test is part of routine newborn screening. But older children and adults can be tested, too.

In adults, a blood sample is drawn from a vein in the arm. In young children and babies, the blood sample is usually collected from a finger or heel. The sample is then sent to a laboratory, where it's screened for the sickle cell form of hemoglobin.

If you or your child has sickle cell anemia, your doctor might suggest other tests to check for possible complications of the disease.

If you or your child carries the sickle cell gene, you'll likely be referred to a genetic counselor.

Assessing stroke risk

A special ultrasound machine can reveal which children have a higher risk of stroke. This painless test, which uses sound waves to measure blood flow in the brain, can be used in children as young as 2 years. Regular blood transfusions can decrease stroke risk.

Tests to detect sickle cell genes before birth

Sickle cell disease can be diagnosed in an unborn baby by sampling some of the fluid surrounding the baby in the mother's womb (amniotic fluid). If you or your partner has sickle cell anemia or the sickle cell trait, ask your doctor about this screening.


Management of sickle cell anemia is usually aimed at avoiding pain episodes, relieving symptoms and preventing complications. Treatments might include medications and blood transfusions. For some children and teenagers, a stem cell transplant might cure the disease.


  • Hydroxyurea (Droxia, Hydrea, Siklos). Daily hydroxyurea reduces the frequency of painful crises and might reduce the need for blood transfusions and hospitalizations. But it can increase the risk of infections. Don't take the drug if you're pregnant.
  • L-glutamine oral powder (Endari). The Food and Drug Administration (FDA) recently approved this drug for treatment of sickle cell anemia. It helps in reducing the frequency of pain crises.
  • Crizanlizumab (Adakveo). This drug, given by injection, can help reduce the frequency of pain crises in adults and children older than 16. Side effects can include nausea, joint pain, back pain and fever.
  • Voxelotor (Oxbryta). This drug is used to treat sickle cell disease in adults and children older than 12. Taken orally, this drug can lower the risk of anemia and improve blood flow throughout the body. Side effects can include headache, nausea, diarrhea, fatigue, rash and fever.
  • Pain-relieving medications. Your doctor might prescribe narcotics to help relieve pain during sickle cell pain crises.

Preventing infections

Children with sickle cell anemia might receive penicillin between the ages of about 2 months old until at least age 5 years. Doing so helps prevent infections, such as pneumonia, which can be life-threatening to children with sickle cell anemia.

Adults who have sickle cell anemia might need to take penicillin throughout their lives if they've had pneumonia or surgery to remove the spleen.

Childhood vaccinations are important for preventing disease in all children. They're even more important for children with sickle cell anemia because their infections can be severe.

Your child's doctor should ensure that your child receives all the recommended childhood vaccinations, as well as vaccines against pneumonia, meningitis, hepatitis B and an annual flu shot. Vaccines are also important for adults with sickle cell anemia.

During the COVID 19 pandemic, people with sickle cell anemia should take extra precautions, such as staying isolated at home as much as possible and for those who are eligible, getting vaccinated.

Surgical and other procedures

  • Blood transfusions. These are used to treat and prevent complications, such as stroke, in people with sickle cell disease.

    In a red blood cell transfusion, red blood cells are removed from a supply of donated blood, then given through a vein to a person with sickle cell anemia. This increases the number of normal red blood cells, which helps reduce symptoms and complications.

    Risks include an immune response to the donor blood, which can make it hard to find future donors; infection; and excess iron buildup in your body. Because excess iron can damage your heart, liver and other organs, you might need treatment to reduce iron levels if you undergo regular transfusions.

  • Stem cell transplant. Also known as bone marrow transplant, this procedure involves replacing bone marrow affected by sickle cell anemia with healthy bone marrow from a donor. The procedure usually uses a matched donor, such as a sibling, who doesn't have sickle cell anemia.

    Because of the risks associated with a bone marrow transplant, including death, the procedure is recommended only for people, usually children, who have significant symptoms and complications of sickle cell anemia. A stem cell transplant is the only known cure for sickle cell anemia.

    Clinical trials are ongoing to address stem cell transplantation in adults and gene therapies.

Clinical trials

Explore Mayo Clinic studies testing new treatments, interventions and tests as a means to prevent, detect, treat or manage this condition.

Self care

Taking the following steps to stay healthy might help you avoid complications of sickle cell anemia:

  • Take folic acid supplements daily and choose a healthy diet. Bone marrow needs folic acid and other vitamins to make new red blood cells. Ask your doctor about a folic acid supplement and other vitamins. Eat a variety of colorful fruits and vegetables, as well as whole grains.
  • Drink plenty of water. Dehydration can increase your risk of a sickle cell crisis. Drink water throughout your day, aiming for about eight glasses a day. Increase the amount of water you drink if you exercise or spend time in a hot, dry climate.
  • Avoid temperature extremes. Exposure to extreme heat or cold can increase your risk of a sickle cell crisis.
  • Exercise regularly, but don't overdo it. Talk with your doctor about how much exercise is right for you.
  • Use nonprescription medications with caution. Use pain medications, such as ibuprofen (Advil, Motrin IB, Children's Motrin, others) or naproxen sodium (Aleve), sparingly, if at all, because of the possible effect on your kidneys. Ask your doctor before taking nonprescription drugs.
  • Don't smoke. Smoking increases your risk of pain crises.

Coping and support

If you or someone in your family has sickle cell anemia, you might consider the following to help you cope:

  • Finding someone to talk with. Living with a chronic illness is stressful. Consider consulting a mental health professional, such as a psychologist, counselor or social worker, to help you cope.
  • Join a support group. Ask your health care provider about support groups for families in your area. Talking with others who are facing challenges similar to yours can be helpful.
  • Exploring ways to cope with the pain. Work with your health care provider to find ways to control your pain. Pain medications can't always take all the pain away. Different techniques work for different people, but it might be worth trying heating pads, hot baths, massages or physical therapy.
  • Learning about sickle cell anemia to make informed decisions about care. If you have a child with sickle cell anemia, learn as much as you can about the disease. Ask questions during your child's appointments. Ask your health care team to recommend good sources of information.

Preparing for your appointment

Sickle cell anemia is usually diagnosed through genetic screening done when a baby is born. Those test results will likely be given to your family doctor or pediatrician. He or she will likely refer you to a doctor who specializes in blood disorders (hematologist) or a pediatric hematologist.

Here's information to help you get ready for your appointment.

What you can do

Make a list of:

  • Your symptoms, including any that seem unrelated to the reason for which you scheduled the appointment, and when they began
  • Key personal information, including family medical history and whether anyone has sickle cell anemia or has the trait for it
  • Questions to ask your doctor

Bring a family member or friend along, if possible, to help you remember the information you're given.

For sickle cell anemia, questions to ask your health care provider include:

  • What's the most likely cause of my child's symptoms?
  • Are there other possible causes?
  • What tests are needed?
  • What treatments are available, and which do you recommend?
  • What side effects are common with these treatments?
  • Are there alternatives to the primary approach that you're suggesting?
  • What's my child's prognosis?
  • Are there dietary or activity restrictions?
  • Do you have brochures or other printed material that I can have? What websites do you recommend?

Don't hesitate to ask other questions.

What to expect from your doctor

Your doctor is likely to ask you questions, including:

  • When did you notice your child's symptoms?
  • Have they been continuous or occasional?
  • What, if anything, seems to improve symptoms?
  • What, if anything, seems to worsen them?

Mar 09, 2022

  1. Sickle cell disease. National Heart, Lung, and Blood Institute. https://www.nhlbi.nih.gov/health-topics/sickle-cell-disease. Accessed Oct. 23, 2021.
  2. Field JJ, et al. Overview of the management and prognosis of sickle cell disease. https://www.uptodate.com/contents/search. Accessed Oct. 21, 2021.
  3. AskMayoExpert. Sickle cell disease. Mayo Clinic; 2021.
  4. Sickle cell disease (SCD). Centers for Disease Control and Prevention. https://www.cdc.gov/ncbddd/sicklecell/index.html. Accessed Oct. 23, 2021.
  5. Onimoe G, et al. Sickle cell disease: A primary care update. Cleveland Clinic Journal of Medicine. 2020; doi:10.3949/ccjm.87a.18051.


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