Test Code NIS Nickel, Serum
Reporting Name
Nickel, SUseful For
Confirmation of an elevated urinary nickel concentration
This test is not useful for the investigation of nickel hypersensitivity.
Performing Laboratory
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Specimen Type
SerumOrdering Guidance
Urine is the preferred specimen type for determining nickel exposure and potential toxicity. Order NIU / Nickel, 24 Hour, Urine or NIUCR / Nickel/Creatinine Ratio, Random, Urine.
This test should not be ordered for the investigation of nickel hypersensitivity. Instead, order testing for lymphocyte proliferation to nickel.
Specimen Required
Patient Preparation: High concentrations of gadolinium and iodine are known to interfere with most metal tests. If either gadolinium- or iodine-containing contrast media has been administered, a specimen should not be collected for 96 hours.
Supplies: Metal Free Specimen Vial (T173)
Collection Container/Tube: Royal blue-top (metal-free, no additive)
Submission Container/Tube: 7-mL Mayo metal-free, screw-capped, vial
Specimen Volume: 0.5 mL
Collection Instructions:
1. Allow the specimen to clot for 30 minutes; then centrifuge the specimen to separate serum from the cellular fraction.
2. Remove the stopper. Carefully pour specimen into a Mayo metal-free, screw-capped vial, avoiding transfer of the cellular components of blood. Do not insert a pipet into the serum to accomplish transfer, and do not ream the specimen with a wooden stick to assist with serum transfer.
3. See Metals Analysis Specimen Collection and Transport for complete instructions.
Specimen Minimum Volume
0.3 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Refrigerated (preferred) | 7 days | METAL FREE |
Ambient | 7 days | METAL FREE | |
Frozen | 7 days | METAL FREE |
Reject Due To
Gross hemolysis | OK |
Gross lipemia | OK |
Gross icterus | OK |
Special Instructions
Reference Values
<2.0 ng/mL
Day(s) Performed
Thursday
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
83885
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
NIS | Nickel, S | 5702-6 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
8622 | Nickel, S | 5702-6 |