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Test ID PBCU Lead/Creatinine Ratio, Urine


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


Reporting Name

Lead/Creatinine Ratio, U

Specimen Type

Urine

Specimen Stability Information

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

Report Available

2 to 4 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

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

Useful For

Detecting clinically significant lead exposure using random urine specimens

 

This test is not a substitute for blood lead screening.

Day(s) Performed

Monday through Friday

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

Specimen Minimum Volume

1.5 mL

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

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)