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Iron, Plasma or Serum
0020037
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Ordering Recommendation
Aid in the diagnosis of iron deficiency anemia and iron overload.
Mnemonic
FE
Methodology
Quantitative Spectrophotometry
Performed
Sun-Sat
Reported
Within 24 hours
New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
Collect
Plasma separator tube or serum separator tube.
Specimen Preparation
Allow specimen to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 2 hours of collection. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.2 mL)
Storage/Transport Temperature
Refrigerated.
Unacceptable Conditions
Specimens collected from patients receiving deferoxamine (wait six hours after last dose). Specimens containing EDTA, sodium/fluoride, oxalate, or sodium citrate. Grossly hemolyzed specimens.
Remarks
Stability
After separation from cells: Ambient: 1 week; Refrigerated: 3 weeks; Frozen: 3 months
Reference Interval
| Age | Reference Interval |
|---|---|
| Newborn 0-6 weeks | 100-250 µg/dL |
| Infant 7 weeks - 11 months | 40-100 µg/dL |
| Child 1 year - 10 years | 50-120 µg/dL |
| Male 11 years and older | 50-170 µg/dL |
| Female 11 years and older | 30-160 µg/dL |
Interpretive Data
No compliance statements are in use for this test.
Note
Hotline History
N/A
CPT Codes
83540
Components
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 0020037 | Iron, Serum or Plasma | 2498-4 |
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
Aliases
- Serum Fe
- Serum Iron
Iron, Plasma or Serum
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