Soluble Transferrin Receptor, Serum or Plasma
Ordering Recommendation
New York DOH Approval Status
Specimen Required
Serum separator tube or plasma separator tube. Also acceptable: green (lithium heparin).
Transfer 1 mL serum or plasma to an ARUP standard transport tube. (Min: 0.4 mL)
Refrigerated.
Contaminated, severely hemolyzed, icteric, or lipemic specimens.
After separation from cells: Ambient: 5 days; Refrigerated: 1 week; Frozen: 1 month (avoid repeated freeze/thaw cycles)
Methodology
Quantitative Chemiluminescent Immunoassay (CLIA)
Performed
Sun-Sat
Reported
Within 24 hours
Reference Interval
Test Number |
Components |
Reference Interval |
---|---|---|
Soluble Transferrin Receptor | Male - 18 years & older: 2.2-5.0 mg/L Female - 18 years & older: 1.9-4.4 mg/L |
Interpretive Data
The Beckman Coulter Access sTfR immunoassay is intended as an aid in the diagnosis of iron deficiency anemia, especially in patients with chronic disease. In adult patients with anemia, an sTfR result greater than or equal to 1.55 mg/L is 86 percent sensitive and 49 percent specific for the presence of iron deficiency anemia, alone or in combination with anemia of chronic disease. The sTfR assay is not intended to be used in isolation; results should be interpreted in conjunction with the patient’s clinical presentation and other diagnostic tests, such as other indicators of iron status (refer to table below).
Test for Changes in: | Iron Deficiency Anemia | Anemia of Chronic Disease | Iron Deficiency & Anemia of Chronic Disease | |
---|---|---|---|---|
Ferritin | Iron Sores | Low | High | Normal or High |
TIBC | Iron Status | High | Low | Normal or High |
Serum Iron | Iron Status | Low | Low | Low |
sTfR | Iron Status | High | Normal | High |
FDA
Note
Hotline History
Hotline History
CPT Codes
84238
Components
Component Test Code* | Component Chart Name | LOINC |
---|---|---|
0070283 | Soluble Transferrin Receptor | 30248-9 |
Aliases
- sTfR
- TfR
- Transferrin Receptor
- Transferrin Receptor Level