Test Code COBRU Cobalt/Creatinine Ratio, Random, Urine
Ordering Guidance
High concentrations of gadolinium and iodine are known to interfere with most metals tests. If either gadolinium- or iodine-containing contrast media has been administered, a specimen should not be collected for 96 hours.
Specimen Required
Supplies: Urine Tubes, 10 mL (T068)
Collection Container/Tube: Clean, plastic urine collection container
Submission Container/Tube: Plastic, 10-mL urine tube or clean, plastic aliquot container with no metal cap or glued insert
Specimen Volume: 3 mL
Collection Instructions:
1. Collect a random urine specimen.
2. See Metals Analysis Specimen Collection and Transport for complete instructions
Useful For
Detecting cobalt exposure in a random urine collection
Monitoring metallic prosthetic implant wear
This test is not useful for assessment of vitamin B12 activity.
Profile Information
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
COBR | Cobalt/Creat Ratio, U | No | Yes |
CRETR | Creatinine, Random, U | No | Yes |
Special Instructions
Method Name
COBR: Inductively Coupled Plasma-Mass Spectrometry (ICP-MS)
CRETR: Enzymatic Colorimetric Assay
Reporting Name
Cobalt/Creat Ratio, Random, USpecimen Type
UrineSpecimen Minimum Volume
2 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Urine | Refrigerated (preferred) | 28 days | |
Frozen | 28 days | ||
Ambient | 14 days |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Reference Values
COBALT:
0-17 years: Not established
>17 years: <1.7 mcg/g Cr
CREATININE:
≥18 years old: 16-326 mg/dL
Reference values have not been established for patients who are younger than 18 years of age.
Performing 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
83018
82570
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
COBRU | Cobalt/Creat Ratio, Random, U | 13468-4 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
607272 | Cobalt/Creat Ratio, U | 13468-4 |
CRETR | Creatinine, Random, U | 2161-8 |
NY State Approved
YesDay(s) Performed
Tuesday, Wednesday, Friday