Sickle cell test

Definition
The sickle cell test looks for the abnormal
Alternative Names
Sickledex; Hgb S test
How the Test is Performed
A
How the Test will Feel
When the needle is inserted to draw blood, some people feel moderate pain. Others feel only a prick or stinging. Afterward, there may be some throbbing or a bruise. This soon goes away.
Why the Test is Performed
This test is done to tell if a person has hemoglobin S which is the abnormal hemoglobin that causes sickle cell disease and sickle cell trait. Hemoglobin is a protein in red blood cells that carries oxygen.
People with sickle cell disease have two abnormal hemoglobin S genes. A person with sickle cell trait has only one of these abnormal genes and no symptoms, or only mild ones.
This test does not tell the difference between these two conditions. Another test, called
Normal Results
A normal test result is called a negative result meaning that there is no hemoglobin S.
Normal value ranges may vary slightly among different labs. Some labs use different measurements or test different samples. Talk to your health care provider about the meaning of your specific test results.
What Abnormal Results Mean
An abnormal test result indicates the person might have one of these:
- Sickle cell disease
- Sickle cell trait
Risks
There is little risk involved with having your blood taken. Veins and arteries vary in size from one person to another, and from one side of the body to the other. Obtaining a blood sample from some people may be more difficult than from others.
Other risks associated with having blood drawn are slight, but may include:
- Excessive bleeding
Fainting or feeling lightheaded- Multiple punctures to locate veins
Hematoma (blood buildup under the skin)- Infection (a slight risk any time the skin is broken)
References
Centers for Disease Control and Prevention website. Get screened to know your sickle cell status.
Centers for Disease Control and Prevention website. Sickle Cell Disease (SCD). About sickle cell disease.
Menapace LA, Thein SL. Clinical aspects of sickle cell disease. In: Hoffman R, Benz EJ, Silberstein LE, et al, eds. Hematology: Basic Principles and Practice. 8th ed. Philadelphia, PA: Elsevier; 2023:chap 43.
Smith-Whitley K, Kwiatkowski JL. Hemoglobinopathies. In: Kliegman RM, St. Geme JW, Blum NJ, et al, eds. Nelson Textbook of Pediatrics. 22nd ed. Philadelphia, PA: Elsevier; 2025:chap 511.
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