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Welcome to Management of Sickle Cell Disease. Post Activity Assessment
Thank you and congratulations for attending this educational activity. Remember, continuous professional development is key to success and professional excellence.
This test is composed of 5 questions based on the information provided to you during the activity. You will have two attempts to complete this test. The 30 minutes which will allow enough time to search for the correct answers.
You must exceed the passing score (60%) in order to receive your certificate
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Sickle cell disease is caused by a mutation in which glutamine is replaced with valine at the sixth position of the beta globin gene (HBB) and is characterized by the production of sickled hemoglobin (HgS). As a result, patients are at an increased risk for complications associated with anemia and vaso-occlusion.CorrectIncorrect
Penicillin prophylaxis oral (125 mg for children younger than 3 years; 250 mg for children 3 years and older) twice daily until 5 years of age in all children with SCA to prevents pneumococcal sepsis.CorrectIncorrect
In sickle cell anemia, hydroxyurea decreases red blood cell (RBC) hemoglobin F levels, RBC water content, and increases adhesion of RBCs to endotheliumCorrectIncorrect