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Test ID BLOD1555 Lead, Venous, with Demographics, Blood

Useful For

Detecting lead toxicity in venous blood specimens

Specimen Type

Whole blood


Ordering Guidance


If testing is needed on a capillary specimen, order PBDC / Lead, Capillary, with Demographics, Blood.



Specimen Required


Patient Preparation: High concentrations of gadolinium and iodine are known to potentially interfere with most inductively coupled plasma mass spectrometry-based metal tests. If either gadolinium- or iodine-containing contrast media has been administered, a specimen should not be collected for 96 hours.

Supplies:

-Metal Free B-D Tube (EDTA), 6 mL (T183)

-Metal Free EDTA 3 mL Tube (T989)

Container/Tube:

Preferred: Royal blue-top BD Vacutainer Plus with EDTA (6 mL) blood collection tube

Acceptable: Royal blue-top BD vacutainer with EDTA blood collection tube (3 mL)

Specimen Volume: 2 mL

Collection Instructions:

1. See Metals Analysis Specimen Collection and Transport  for complete instructions.

2. Send whole blood specimen in original tube. Do not aliquot.


Specimen Minimum Volume

0.1 mL

Reject Due To

Gross hemolysis OK
Gross lipemia OK
Gross icterus OK
Clotted blood Reject

Specimen Stability Information

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

Day(s) Performed

Monday through Saturday

Report Available

1 to 2 days

Method Name

Inductively Coupled Plasma Mass Spectrometry (ICP-MS)

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

83655

Forms

1. Lead and Heavy Metals Reporting (T491) or Lead and Heavy Metals Reporting-Spanish (T956)

2. If not ordering electronically, complete, print, and send a General Request (T239) with the specimen.

Secondary ID

113401

Profile Information

Test ID Reporting Name Available Separately Always Performed
PBBV Lead, Venous, B No Yes
DEMO8 Patient Demographics No Yes

Reporting Name

Lead, Venous, w/Demographics, B

Reference Values

<3.5 mcg/dL

Critical values

Pediatrics (≤15 years): ≥20.0 mcg/dL

Adults (≥16 years): ≥70.0 mcg/dL

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.
Sanford Laboratories - Fargo Additional Information:

SANFORD INTERFACE BUILD INFORMATION

Result Code Result Code Description
22781 Lead, Venous, B
22782 Venous/Capillary
22783 Street Address
22784 City
22785 State
22786 Zip
22787 County
22788 Home Phone
22789 Race
22790 Patient Ethnicity
22791 Patient Occupation
22792 Patient Employer
22793 Guardian First Name
22794 Guardian Last Name
22795 Health Care Provider Name
22796 Health Care Provider Street Address
22797 Health Care Provider Ctiy
22798 Health Care Provider State
22799 Health Care Provider Zip Code
22800 Health Care Provider Phone
22801 Submitting Laboratory Phone