Lead, Whole Blood (Capillary by ICP-MS)
Label Mnemonic: | LEADCAP |
Epic code: | LAB9114 |
Order form: | Laboratory Requisition |
Supply order: | Supply Order Form |
Billing: | Billing Policies |
CPT code: | 83655 |
Specimen(s):
Whole Blood
Collection Medium:
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Lavender top tube 0.5 mL (EDTA) |
Minimum:
Clean puncture site well with soap and water before collection
procedure begins. Invert specimen 10 times to prevent clot
formation.
Preferred Minimum: One FULL Lavender 0.5 mL (EDTA) top tube.
Absolute Minimum: 0.3 mL whole blood
Preferred Minimum: One FULL Lavender 0.5 mL (EDTA) top tube.
Absolute Minimum: 0.3 mL whole blood
Rejection Criteria:
Specimens collected in tubes other than Lavender Pediatric (EDTA).
Specimens transported in tubes other than trace-element free
transport tubes or Lavender Pediatric (EDTA) tubes. Heparin
anticoagulant. Clotted specimens.
Turn Around Time:
1-3 days upon receipt at reference laboratory
Reference Range:
Concentration Comment 5-9.9 μg/dL Adverse health effects are possible, particularly in children under 6 years of age and pregnant women. Discuss health risks associated with continued lead exposure. For children and women who are or may become pregnant, reduce lead exposure. All ages 10-19.9 μg/dL Reduced lead exposure and increased biological monitoring are recommended. All ages 20-69.9 μg/dL Removal from lead exposure and prompt medical evaluation are recommended. Consider chelation therapy when concentrations exceed 50 μg/dL and symptoms of lead toxicity are present. All ages >44.9 μg/dL Critical. Immediate medical evaluation is recommended. Consider chelation therapy when symptoms of lead toxicity are present. Less than 19 years of age >69.9 μg/dL Critical. Immediate medical evaluation is recommended. Consider chelation therapy when symptoms of lead toxicity are present. Greater than 19 years of age
Interpretive Data:
Elevated results may be due to skin or collection-related
contamination, including the use of a noncertified lead-free
collection/transport tube. If contamination concerns exist due to
elevated levels of blood lead, confirmation with a venous specimen
collected in a certified lead-free tube is recommended.
Repeat testing is recommended prior to initiating chelation therapy or conducting environmental investigations of potential lead sources. Repeat testing collections should be performed using a venous specimen collected in a certified lead-free collection tube.
Information sources for reference intervals and interpretive comments include the "CDC Response to the 2012 Advisory Committee on Childhood Lead Poisoning Prevention Report" and the "Recommendations for Medical Management of Adult Lead Exposure, Environmental Health Perspectives, 2007." Thresholds and time intervals for retesting, medical evaluation, and response vary by state and regulatory body. Contact your State Department of Health and/or applicable regulatory agency for specific guidance on medical management recommendations.
This test was developed and its performance characteristics determined by reference laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Repeat testing is recommended prior to initiating chelation therapy or conducting environmental investigations of potential lead sources. Repeat testing collections should be performed using a venous specimen collected in a certified lead-free collection tube.
Information sources for reference intervals and interpretive comments include the "CDC Response to the 2012 Advisory Committee on Childhood Lead Poisoning Prevention Report" and the "Recommendations for Medical Management of Adult Lead Exposure, Environmental Health Perspectives, 2007." Thresholds and time intervals for retesting, medical evaluation, and response vary by state and regulatory body. Contact your State Department of Health and/or applicable regulatory agency for specific guidance on medical management recommendations.
This test was developed and its performance characteristics determined by reference laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Comments:
Recommended for routine testing for lead exposure in pediatric
populations. Confirm elevated results with Lead, Venous Confirmation
by ICP-MS.
Methodology:
Quantitative Inductively Coupled Plasma/Mass Spectrometry
Instructions:
Invert specimen 10 times to prevent clot formation.
Sample Processing:
Submit whole blood in original container.
DO NOT CENTRIFUGE.
Sample Storage:
Room Temperature.
Transport Instructions:
Place labeled specimen into zip-lock type biohazard bag; seal
bag.
Place completed laboratory requisition (or packing list) into outside pocket of bag.
Ship at room temperature.
Place completed laboratory requisition (or packing list) into outside pocket of bag.
Ship at room temperature.
See also:
Lead, Venous Confirmation by ICP-MS, Whole Blood
Lead, Venous Confirmation by ICP-MS, Whole Blood