Chromium, Serum

Test Code
CHROM


Alias/See Also

LAB967



CPT Codes
<p>82495</p>

Preferred Specimen

Specimen Type: Serum

Collection Container/Type: Plain, royal blue-top Vacutainer plastic trace element blood collection tube

Submission Container/Tube: Metal-free, screw-capped, plastic vial

Specimen Volume: 2 mL

Collection Instructions: 

  1. Draw one (royal blue-top) tube of blood and discard.
  2. Draw second (royal blue-top) tube.
  3. Allow blood to clot in an upright position.
  4. Centrifuge and pour (do not pipette) the serum into a metal-free tube.

Additional Information:

  • Tests performed on a specimen submitted in a nontrace element tube or nonacid-washed/nonmetal-free container may not accurately reflect the patients level.
  • If a nontrace element tube/container is received, it will be accepted for testing; however, elevated results are reported with the message that resubmission with a trace element tube/container is recommended.


Minimum Volume

1 mL



Instructions
Draw one (royal blue-top) tube of blood and discard. Draw second (royal blue-top) tube. Allow blood to clot in an upright position. Centrifuge and pour (do not pipette) the serum into a metal-free tube.

Tests performed on a specimen submitted in a nontrace element tube or nonacid-washed/nonmetal-free container may not accurately reflect the patient's level. If a nontrace element tube/container is received, it will be accepted for testing; however, elevated results are reported with the message that resubmission with a trace element tube/container is recommended.


Transport Temperature
Refrigerated (cold packs)


Specimen Stability

Room temperature: 5 days

Refrigerated: 10 days

Frozen: 21 days



Methodology

Inductively Coupled Plasma/Mass Spectrometry (ICP/MS)

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.



FDA Status
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Setup Schedule
Set up: Sun-Fri; Report available: 1 day


Report Available

1 day



Reference Range
≤1.4 mcg/L


Clinical Significance
Occupational exposure and exposure to environmental contamination of Chromium may lead to toxicity. The need for Chromium supplements is unproven. Supplements taken in excess may also lead to Chromium toxicity.


Performing Laboratory
Quest Diagnostics Nichols Institute 14225 Newbrook Drive Chantilly, VA 20153


Last Updated: October 15, 2019


The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.