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Geisinger Medical Laboratories Test Catalog
KLEIHAUER BETKE |
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Geisinger Epic Procedure Code: LAB2574
Geisinger Epic ID: 7184
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SPECIMEN COLLECTION |
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Specimen type: |
Whole Blood | ||||||||||||||||||||||||||||
Preferred collection container: |
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Alternate Collection Container: |
Lavender-top (K2 EDTA) microcollection tube
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Specimen required: |
Preferred specimen is a 3 mL EDTA lavender-top tube. One EDTA lavender-top microcollection tube is acceptable for difficult draws. Minimum acceptable will be 250 uL (microcollection tube has lines to indicate the 250 and 500 uL volumes). | ||||||||||||||||||||||||||||
| SPECIMEN PROCESSING |
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Specimen processing instructions: |
Do not centrifuge. | ||||||||||||||||||||||||||||
Transport temperature: |
Refrigerated (preferred) or room temperature. | ||||||||||||||||||||||||||||
Specimen stability: |
Specimen stable for two weeks if refrigerated. | ||||||||||||||||||||||||||||
Rejection criteria: |
Frozen, clotted, hemolyzed, or centrifuged specimen. | ||||||||||||||||||||||||||||
TEST DETAILS |
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Reference interval: |
<1.0% | ||||||||||||||||||||||||||||
Interpretation guide: |
Rh Immunoglobulin Dosing
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CPT code(s): |
85460 | ||||||||||||||||||||||||||||
| Note: The billing party has sole responsibility for CPT coding. Any questions regarding coding should be directed to the payer being billed. The CPT codes provided by GML are based on AMA guidelines and are for informational purposes only. | |||||||||||||||||||||||||||||
Test includes: |
Percent of fetal red cells, recommended RhoGAM dosages. | ||||||||||||||||||||||||||||
Methodology: |
Acid elution test |
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Synonyms: |
Kleihauer-Betke Stain, Fetaldex, test for fetomaternal hemorrhage, FETAL HGB RBC STAIN (Kleihauer Betke), FHGBS, Fetal Hemorrhage, count, Hemorrhage, Hemoglobin, Fetomaternal
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Clinical significance: |
Used to detect fetal hemoglobin (hemoglobin F) and dose Rh immunoglobulin in Rh negative women with a positive fetal hemoglobin screen. Elevated hemoglobin F levels occur from fetomaternal hemorrhage, hemoglobinopathies (sickle cell disease, hereditary persistence of hemoglobin F, etc.) or in patients taking medications that increase hemoglobin F production (hydroxyurea, etc.). | ||||||||||||||||||||||||||||
Doctoral Director(s:) |
Mary Dhesi MD | ||||||||||||||||||||||||||||
| Review Date: | 01/25/2023 | ||||||||||||||||||||||||||||
Performing Locations
Geisinger Wyoming Valley Medical Center