Test Code TIUCR Titanium/Creatinine Ratio, Random, Urine
Shipping Instructions
Ship specimen on ice
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, the specimen should not be collected for at least 96 hours.
Supplies: Urine Tubes, 10 mL (T068)
Collection Container/Tube: Clean, plastic urine collection container
Submission Container/Tube: Plastic, 10-mL urine tube or a clean, plastic aliquot container with no metal cap or glued insert
Specimen Volume: 7 mL
Collection Instructions:
1. Collect a random urine specimen.
2. See Metals Analysis Specimen Collection and Transport for complete instructions.
Useful For
Monitoring exposure and elimination of titanium
Profile Information
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
TICU | Titanium/Creat Ratio, U | No | Yes |
CRTFR | Creatinine, Random, U | No | Yes |
Special Instructions
Method Name
TICU: Triple-Quadrupole Inductively Coupled Plasma-Mass Spectrometry (ICP-MS/MS)
CRTFR: Enzymatic Colorimetric Assay
Reporting Name
Titanium/Creat Ratio, Random, USpecimen Type
UrineSpecimen Minimum Volume
2 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Urine | Frozen | 28 days |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Reference Values
TITANIUM
0-17 years: Not established
≥18 years: <0.4 mcg/g creatinine
CREATININE
≥18 years old: 16-326 mg/dL
Reference values have not been established for patients who are less than 18 years of age.
Interpretation
Elevated concentrations of urinary titanium have been reported after documented exposures.
Day(s) Performed
Wednesday
Report Available
1 to 7 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest 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
82570
83018
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
TIUCR | Titanium/Creat Ratio, Random, U | 104656-4 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
CRTFR | Creatinine, Random, U | 2161-8 |
614615 | Titanium/Creat Ratio, U | 104656-4 |