Epic Test Code LAB829 Iron Binding Capacity, Total (TIBC)
Performing Location(s)
BMC
Specimen Type
Serum
Preferred Container
Gold or Red top tube
Blood Tube Draw Volume
Min 50% draw volume
Minimum Volume to Submit for Testing
0.5 mL Serum
- Multiple test can be performed from this volume. For question please contact the lab at 547-3975.
Storage Requirements
Sample tubes should be centrifuged within 2 hour of collection followed by transfer of the serum (red or gold top) or plasma (green top) to a labeled plastic, aliquot tube
See Causes of Rejection for temperature requirements.
Transportation Needs
Deliver specimen to the laboratory within 1 hour of collection. If not possible see “Storage Requirements”
Causes for Rejection
Mislabeled or unlabeled specimen
Less than 50% draw for Vacutainer tubes
>7 days refrigerated
> 4 days Room Temperature
> 40 days Frozen
Hemolysis > 50 mg/dL HgB
Lipemia > 4000 mg/dL Trig
Bilirubin > 40 mg/dL Bili
Heparin, EDTA, NaF
Limitations
Ferrous sulfate at 250 µg/dL increased IBCT results by 17%.
Interference from icterus (bilirubin 60 mg/dL [1026 mmol/L]),c hemolysis (hemoglobin 250 mg/dL [0.16 mmol/L] (monomer)) and lipemia 600 mg/dL [6.8 mmol/L] was less than 10% at a total iron binding capacity level of 260 µg/dL.
Reference Values
Population | Units | Reference Range |
All populations | ug/dL | 250 - 450 |
TIBC (ug/dL) = Transferrin (mg/dL) x 1.4
Days of Analysis
All
Available STAT
No
Additional Information
Patient Preparation:
Blood should be collected after a 12-hour period of fasting by normal procedures
Contraindications:
Measurements of IBCT may be inaccurate if performed within 14 days of IV iron dextran administration. Studies have shown that gadodiamide containing contrast media used in Magnetic Resonance Imaging (MRI) can produce analytic interference, both positive and negative, with assays performed in the clinical Laboratory for Calcium, Iron Magnesium, TIBC and Zinc. The package insert for Gadodiamide recommends waiting 12 to 24 hours between contrast agent administration and blood specimen collection to ensure that the contrast agent has been cleared. A longer waiting period might be necessary for patients with renal insufficiency. The average half-life of gadodiamide in patients with severely reduced renal function is 34 hours Miscellaneous Information: Percent Iron Saturation (aka Percent Transferrin Saturation) is calculated as follows: Iron Saturation (%) = (Serum Iron x 100 ) / TIBC
The measurement of serum iron, iron binding capacity, and iron (transferrin) saturation are only useful in screening for chronic iron overload diseases and for confirmation and monitoring of acute iron poisoning in children. Many factors influence serum iron concentration and TIBC. Changes that may be observed in various physiological or pathological conditions include: diurnal variation, menstrual cycle, pregnancy, ingestion of iron (including iron-fortified vitamins), oral contraceptives (progesterone-like), iron dextran injection, hepatitis, acute and chronic inflammation, iron deficiency, and iron overload (hemochromatosis). Furthermore, individuals with iron deficiency may have normal values for serum iron and TIBC. For these reasons, assays for serum iron, iron binding capacity and iron (transferrin) saturation should not be used as a test for iron deficiency.
Additional Information:
Serum should be removed from cells within 2 hours of venipuncture
Sample tubes should be centrifuged within 2 hours of collection followed by transfer of the serum (red or gold top) to a labeled plastic, aliquot tube.
This test is not available on a STAT basis. If an emergency request is necessary, call 3731 for availability. Pathologist approval may be required.
Methodology
Beckman AU/Dx Series
CPT Code
84466
Last Updated
20-Jan-20