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Test Code CURCU Copper/Creatinine Ratio, Random, Urine

Additional Codes

Internal / External / Beaker: LAB5300


Specimen Required


Patient Preparation: High concentrations of barium are known to interfere with most metal tests. If barium-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 with no metal cap or glued insert

Submission Container/Tube: Plastic, 10-mL urine tube or a 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.


Secondary ID

615257

Useful For

Investigation of Wilson disease and obstructive liver disease using a random urine specimen

Profile Information

Test ID Reporting Name Available Separately Always Performed
CURC Copper/Creat Ratio, U No Yes
CRETR Creatinine, Random, U No Yes

Method Name

CURC: Triple-Quadrupole Inductively-Coupled Plasma Mass Spectrometry (ICP-MS/MS)

CRETR: Enzymatic Colorimetric Assay

Reporting Name

Copper/Creat Ratio, Random, U

Specimen Type

Urine

Specimen 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

COPPER/CREATITINE:

Males:

0-17 years: Not established

≥18 years: 9-43 mcg/g creatinine

Females:

0-17 years: Not established

≥18 years: 7-72 mcg/g creatinine

 

CREATITINE:

≥18 years old: 16-326 mg/dL

Reference values have not been established for patients who are younger than 18 years.

Day(s) Performed

Monday, Thursday

Report Available

2 to 5 days

Performing 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

82525

82570

LOINC Code Information

Test ID Test Order Name Order LOINC Value
CURCU Copper/Creat Ratio, Random, U 13829-7

 

Result ID Test Result Name Result LOINC Value
615258 Copper/Creat Ratio, U 13829-7
CRETR Creatinine, Random, U 2161-8