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Test ID: HCR S

Chromium, Serum

Test Overview

Clinical Utility

Serum Chromium concentrations can be used for nutritional assessment in patients on TPN. Serum concentration reflects day-to-day Chromium variations. The measurement of Chromium in erythrocytes provides a better index of body content than the measurement of Chromium in serum. Whole blood Chromium is recommended for monitoring following orthopedic arthroplasty.

Method

Inductively coupled plasma-triple quadrupole mass spectrometry (ICP-TripleQ MS)

Result Included

Chromium

Specimen

Specimen Type

Serum

Containers

Preferred Containers

BD 6 ml Non Additive Royal Blue Vacutainer (Reference # 368380)

Volume

Sample Volume

2 mL

Collection & Handling

Collection Instructions

Collect serum in contaminant-free tube with clot-activator. Avoid hemolysis.

Handling Information

Separate as soon as possible and transfer serum to polypropylene vial. Store and send cold.

Additional Information

Concentrations of chromium are higher in erythrocytes than in serum. The results in serum may be falsely elevated if not separated within 30 m and/or hemolysis is present.

Rejection Criteria

Criteria Specification
Hemolysis Visible

Performance & Interpretation

Turnaround Time

10 days

Results

Name
Units
Reference Range
Conversion
  1. Chromium
    nmol/L
    1.9 - 3.8
    ng/L x 0.0192

Referral Location

Canada

Test Version

Last Updated

2019-09-30