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Test Code PBCU Lead/Creatinine Ratio, Urine

Reporting Name

Lead/Creatinine Ratio, U

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Useful For

Detecting clinically significant lead exposure using random urine specimens

 

This test is not a substitute for blood lead screening.

Method Name

Only orderable as part of profile. For more information see:

-PBUCR / Lead/Creatinine Ratio, Random, Urine

-HMUCR / Heavy Metal/Creatinine Ratio, with Reflex, Random, Urine

 

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


Specimen Required


Only orderable as part of profile. For more information see:

-PBUCR / Lead/Creatinine Ratio, Random, Urine

-HMUCR / Heavy Metal/Creatinine Ratio, with Reflex, Random, Urine


Specimen Type

Urine

Specimen Minimum Volume

1.5 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Urine Refrigerated (preferred) 28 days
  Ambient  28 days
  Frozen  28 days

Reject Due To

  All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.

Reference Values

Only orderable as part of profile. For more information see:

-PBUCR / Lead/Creatinine Ratio, Random, Urine

-HMUCR / Heavy Metal/Creatinine Ratio, with Reflex, Random, Urine

 

0-17 years: Not established

≥18 years: <2 mcg/g creatinine

Interpretation

Urinary excretion of less than 4 mcg/g creatinine is not associated with any significant lead exposure.

 

Urinary excretion greater than 4 mcg/g creatinine is usually associated with pallor, anemia, and other evidence of lead toxicity.

 

Measurements of urinary lead levels have been used to assess lead exposure. However, like lead blood, urinary lead excretion mainly reflects recent exposure and thus shares many of the same limitations for assessing lead body burden or long-term exposure.(1,2)

 

Urinary lead concentration increases exponentially with blood lead and can exhibit relatively high intra-individual variability, even at similar blood lead concentrations.(3,4)

Day(s) Performed

Monday through Friday

Report Available

2 to 4 days

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

83655

LOINC Code Information

Test ID Test Order Name Order LOINC Value
PBCU Lead/Creatinine Ratio, U 13466-8

 

Result ID Test Result Name Result LOINC Value
608904 Lead/Creatinine Ratio, U 13466-8