Ferritin
Label Mnemonic: FRTN
Epic Lab Code: LAB68
Downtime Form: A-1a General Laboratory Requisition
Chemistry
6240 RCP
356-3527
Specimen(s):
Plasma
Collection Medium:
Plasma Separator Tube 4.5 mL
Alternate Collection Media:
Call laboratory for additional acceptable specimen collection containers.
Minimum:
3 mL whole blood from light green top tube or TWO Microtainer® devices.
Testing Schedule:
24 hrs/day, 7 days a week, including holidays.
Turn Around Time:
1 hour (upon receipt in laboratory)
Reference Range:
Manufacturer's reference range: Adult male 30 - 400 ng/mL Adult female 13 - 150 ng/mL See also: Am J Clin Path, 70: 79, 1978; Can Med Assoc J, 114: 417, 1976 Iron deficiency 0-20 ng/mL
Comments:
Refer to BD Microtainer® Tubes product sheet for detailed sample collection instructions.
Test Limitations:
The assay is unaffected by icterus (bilirubin is less than 65 mg/dL), hemolysis (Hb is less than 500 mg/dL), lipemia (Intralipid is less than 3300 mg/dL) and biotin is less than 50 ng/ml. (criterion: recovery within plus or minus 10% of initial value). In patients receiving therapy with high biotin doses (i.e. is greater than 5 mg/day) no sample should be taken until at least 8 hours after the last biotin administration. No interference was observed from rheumatoid factors up to a concentration of 2500 U/mL. No high dose hook effect at ferritin concentrations of up to 100 000 ng/mL. In vitro tests were performed on 19 commonly used pharmaceuticals. No interference with the assay was found. Iron2+- and iron3+-ions at therapeutic concentrations do not interfere in the Ferritin assay. As with all tests containing monoclonal antibodies, erroneous findings may be obtained from samples taken from patients who have been treated with monoclonal mouse antibodies or who have received them for diagnostic purposes. Ferritin contains additives which minimize these effects. In rare cases interference due to extremely high titers of antibodies to streptavidin and ruthenium can occur. For diagnostic purposes, the Ferritin findings should always be assessed in conjunction with the patient's medical history, clinical examination and other findings.
Methodology:
Electrochemiluminescence Immunoassay
CPT Code:
82728