Test Code AL Aluminum, Serum
Additional Codes
Mayo Test ID |
---|
AL |
Reporting Name
Aluminum, SUseful For
Preferred monitoring for aluminum toxicity in patients undergoing dialysis
Preferred test for routine aluminum screening
Monitoring metallic prosthetic implant wear
Method Name
Dynamic-Reaction Cell Inductively-Coupled Plasma Mass Spectrometry (DRC-ICP-MS)
Performing Laboratory
Mayo Clinic Laboratories in RochesterSpecimen Type
SerumSpecimen 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 B-D Tube (No Additive), 6 mL (T184)
-Metal Free Specimen Vial (T173)
Container/Tube: 6-mL Plain, royal blue-top Vacutainer plastic trace element blood collection tube
Submission Container/Tube: 7-mL Metal-free, screw-capped, polypropylene vial
Specimen Volume: 1.2 mL
Collection Instructions: 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
<7 ng/mL
<60 ng/mL (dialysis patients)
For International System of Units (SI) conversion for Reference Values, see www.mayocliniclabs.com/order-tests/si-unit-conversion.html
Day(s) Performed
Tuesday
CPT Code Information
82108
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
AL | Aluminum, S | 5574-9 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
8373 | Aluminum, S | 5574-9 |
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.Report Available
2 to 8 daysForms
If not ordering electronically, complete, print, and send a Renal Diagnostics Test Request (T830) with the specimen.