Student Athletes with Sickle Cell Trait Should Take Precautions When Training
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Treatment
Basic treatment of sickle cell crisis includes:
- Bedrest
- Pain relief medications
- Oral and intravenous fluids
- Oxygen—to reduce pain and prevent complications
In addition, treatment may include:
Penicillin
Newborns with sickle cell disease may be given penicillin. It is given twice a day, beginning at age two months. It is continued until at least five years of age.
Pneumococcal Vaccine
It is recommended that children with sickle cell disease who are 2-5 years of age receive pneumococcal vaccine (PCV-7).
Hydroxyurea (Hydrea)
This is the first drug to significantly prevent complications of sickle cell disease.
It increases the production of fetal hemoglobin. This decreases the number of deformed red blood cells. As a result, it reduces the frequency of sickle cell crisis.
Hydrea is not appropriate for everyone with sickle cell disease. It is only recommended for people over age 18 who have had at least three painful crises in the previous year.
Blood Transfusions
Blood transfusions can treat and prevent some of the complications. Regular transfusion therapy can help prevent recurring strokes in children.
Bone Marrow Transplant
A bone marrow transplant from a matched donor may be effective. There are medical risks involved. Recipients must also take drugs that suppress the immune system for the rest of their lives.
If you or your child is diagnosed with sickle cell anemia, follow your doctor's instructions .
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition. Copyright © 2024 EBSCO Publishing All rights reserved.