Iron, Plasma or Serum
Also known as: FE
Use
This test aids in the diagnosis of iron deficiency anemia and iron overload. It measures the concentration of iron in the plasma or serum, which can be indicative of various health conditions related to iron imbalance.
Special Instructions
Not provided.
Limitations
Tests may be compromised if specimens are collected from patients receiving deferoxamine if taken within six hours before the test. Additionally, the presence of EDTA, sodium/fluoride, oxalate, sodium citrate, or gross hemolysis can cause specimen rejection due to interference with test results.
New York Approved
Methodology
Automated Analyzer
Biomarkers
LOINC Codes
- 2498-4 - Iron SerPl-mCnc
Result Turnaround Time
1 day
Related Documents
For more information, please review the documents below
Specimen
Plasma
Volume
1 mL
Minimum Volume
0.2 mL
Container
ARUP Standard Transport Tube
Collection Instructions
Allow specimen to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 2 hours of collection.
Storage Instructions
Refrigerated.
Causes for Rejection
Specimens collected from patients receiving deferoxamine within six hours. Specimens containing EDTA, sodium/fluoride, oxalate, or sodium citrate. Grossly hemolyzed specimens.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 1 week |
| Refrigerated | 3 weeks |
| Frozen | 3 months |
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