Reference range(s)
The reference ranges listed below are valid on this date of January 28, 2025.
Component | Age | Male Norm | Male Critical Low | Male Critical High | Female Norm | Female Critical High | Female Critical Low | Units | Add'l info |
---|---|---|---|---|---|---|---|---|---|
Arsenic, Blood | ALL | < or = 12.0 ug/L | < or = 12.0 ug/L | ug/L | Elevated... Note1 | ||||
Lead, Blood | >=6Y | < or = 4.9 ug/dL | < or = 4.9 ug/dL | ug/dL | Analysis ... Note2 | ||||
Lead, Blood | 0-5Y | < or = 3.4 ug/dL | < or = 3.4 ug/dL | ug/dL | Analysis ... Note2 | ||||
Mercury, Whole Blood | ALL | < or = 10.0 ug/L | < or = 10.0 ug/L | ug/L | Elevated... Note3 |
Note1:
Elevated results may be due to skin or collection-related contamination, including the use of a noncertified metal-free collection/transport tube. If contamination concerns exist due to elevated levels of blood arsenic, confirmation with a second specimen collected in a certified metal-free tube is recommended
Potentially toxic ranges for blood arsenic: Greater than or equal to 600 ug/L
Blood arsenic is for the detection of recent exposure poisoning only. Blood arsenic levels in healthy subjects vary considerably with exposure to arsenic in the diet and the environment. A 24- hour urine arsenic is useful for the detection of chronic exposure
This test was developed and its performance characteristics determined by ARUP 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
.
Note2:
Analysis performed by Inductively Coupled Plasma-Mass Spectrometry
(ICP-MS).
Elevated results may be due to skin or collection-related
contamination, including the use of a noncertified lead-free
tube. If contamination concerns exist due to elevated levels of
blood lead, confirmation with a second specimen collected in a
certified lead-free tube is recommended.
Information sources for blood lead reference intervals and
interpretive comments include the CDC's "Childhood Lead
Poisoning Prevention: Recommended Actions Based on Blood
Lead Level" and the "Adult Blood Lead Epidemiology and
Surveillance: Reference Blood Lead Levels (BLLs) for Adults in
the U.S." 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.
Group Concentration Comment
Children 3.5-19.9 ug/dL Children under the age of 6
years are the most vulnerable
to the harmful effects of
lead exposure. Environmental
investigation and exposure
history to identify potential
sources of lead. Biological
and nutritional monitoring
are recommended. Follow-up
blood lead monitoring is
recommended.
20-44.9 ug/dL Lead hazard reduction and
prompt medical evaluation are
recommended. Contact a
Pediatric Environmental
Health Specialty Unit or
poison control center for
guidance.
Greater than Critical. Immediate medical
44.9 ug/dL evaluation, including
detailed neurological exam is
recommended. Consider
chelation therapy when
symptoms of lead toxicity are
present. Contact a Pediatric
Environmental Health
Specialty Unit or poison
control center for
assistance.
Adult 5-19.9 ug/dL Medical removal is
recommended for pregnant
women or those who are trying
or may become pregnant.
Adverse health effects are
possible. Reduced lead
exposure and increased blood
lead monitoring are
recommended.
20-69.9 ug/dL Adverse health effects are
indicated. Medical removal
from lead exposure is
required by OSHA if blood
lead level exceeds 50 ug/dL.
Prompt medical evaluation is
recommended.
Greater than Critical. Immediate medical
69.9 ug/dL evaluation is recommended.
Consider chelation therapy
when symptoms of lead
toxicity are present.
This test was developed and its performance characteristics
determined by ARUP Laboratories. It has not been cleared or
approved by the U.S. Food and Drug Administration. This test
was performed in a CLIA-certified laboratory and is intended
for clinical purposes.
.
Note3:
Elevated results may be due to skin or collection-related contamination, including the use of a noncertified metal-free collection/transport tube. If contamination concerns exist due to elevated levels of blood mercury, confirmation with a second specimen collected in a certified metal-free tube is recommended
Blood mercury levels predominantly reflect recent exposure and are most useful in the diagnosis of acute poisoning as blood mercury concentrations rise sharply and fall quickly over several days after ingestion. Blood concentrations in unexposed individuals rarely exceed 20 ug/L. The provided reference interval relates to inorganic mercury concentrations. Dietary and non-occupational exposure to organic mercury forms may contribute to an elevated total mercury result. Clinical presentation after toxic exposure to organic mercury may include dysarthria, ataxia and constricted vision fields with mercury blood concentrations from 20 to 50 ug/L
This test was developed and its performance characteristics determined by ARUP 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
.