Beutler test
Beutler Test is a medical diagnostic procedure used to detect G6PD deficiency, a genetic disorder that affects the red blood cells. The test is named after its developer, Ernest Beutler, a renowned American hematologist.
Overview[edit | edit source]
The Beutler Test is a Fluorescent Spot Test (FST) that identifies the presence of glucose-6-phosphate dehydrogenase (G6PD) in red blood cells. G6PD is an enzyme that protects red blood cells from potentially harmful byproducts of certain medications or foods. A deficiency in this enzyme can lead to hemolytic anemia, a condition where red blood cells are destroyed faster than they can be replaced.
Procedure[edit | edit source]
The Beutler Test involves taking a blood sample from the patient. The blood is then treated with a substance that causes red blood cells to break down if G6PD is deficient. The presence of hemolysis, or red blood cell breakdown, is then detected under a microscope.
Interpretation[edit | edit source]
A positive Beutler Test indicates a deficiency in G6PD. This can confirm a diagnosis of G6PD deficiency, which can help guide treatment decisions and dietary recommendations. A negative test, on the other hand, suggests that the patient's G6PD levels are normal.
Limitations[edit | edit source]
While the Beutler Test is a valuable tool in diagnosing G6PD deficiency, it has its limitations. For instance, it may not detect mild cases of the deficiency. Additionally, the test may yield false-negative results if the patient has recently had a blood transfusion or if the blood sample is not properly handled.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD