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HelpTest ID TICU Titanium/Creatinine Ratio, Urine
Specimen Required
Only orderable as part of a profile. For more information see TIUCR / Titanium/Creatinine Ratio, Random, Urine.
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 Trace Metals Analysis Specimen Collection and Transport for complete instructions.
Useful For
Measurement of titanium concentration as part of a profile to assess exposure and elimination of titanium
Method Name
Only orderable as part of a profile. For more information see TIUCR / Titanium/Creatinine Ratio, Random, Urine.
Inductively Coupled Plasma-Mass Spectrometry (ICP-MS)
Reporting Name
Titanium/Creat Ratio, USpecimen Type
UrineSpecimen Minimum Volume
1 mL
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Urine | Frozen | 28 days |
Reference Values
Only orderable as part of a profile. For more information see TIUCR / Titanium/Creatinine Ratio, Random, Urine.
0-17 years: Not established
≥18 years: <0.4 mcg/g Cr
Day(s) Performed
Wednesday
Report Available
1 to 7 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
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
83018
LOINC Code Information
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 614615 | Titanium/Creat Ratio, U | 104656-4 |