Erythropoietin
Erythropoietin (EPO), Serum
Test
Method
Immunoassay
Report Includes
Specimens
Serum
Clinical Utility
Elevated levels of serum erythropoietin (EPO) occur in patients with anemias due to increased red cell destruction in hemolytic anemia and also in secondary polycythemias associated with impaired oxygen delivery to the tissues, impaired pulmonary oxygen exchange, abnormal hemoglobins with increased oxygen affinity, constriction of the renal vasculature, and inappropriate EPO secretion caused by certain renal and extrarenal tumors. Normal or depressed levels may occur in anemias due to increased oxygen delivery to tissues, in hypophosphatemia, and in polycythemia vera.
Test Location
Quest Diagnostics, California USA
Test Version
30-Sep-2019
Specimen
Specimens
Serum
Sample Volume
1 mL
Minimum Volume
0.5 mL
Specimen Comment
Plasma is not suitable.
Collection & Handling
Collection Instructions
Due to diurnal variation, it is recommended that specimens be collected between 7:30 a.m. and noon. Repeat collections should be timed appropriately.
Handling Information
Store and send frozen.
Stability
Ambient | 10 days |
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Refrigerated | 18 days |
Frozen | 28 days |
Rejection Criteria
Specimen | Plasma |
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Test Version
30-Sep-2019
Performance / Interpretation
Method
Immunoassay
Turnaround Time
6 days
Results
Name | Units | Reference Range | Conversion Factor | |
---|---|---|---|---|
Erythropoietin | mIU/mL |
|
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Reference ranges may not be valid and are not applicable if the patient is receiving recombinant erythropoietin.
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Test Location
Quest Diagnostics, California USA
Test Version
30-Sep-2019
Interface / Setup
HL7 Interface Codes
Order Code | Result Codes | Units |
---|---|---|
EPOQST | 39230Erythropoietin | mIU/mL |
Test Version
30-Sep-2019