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Test ID: HCR P

Chromium, Plasma

Test Overview

Clinical Utility

Plasma Chromium concentrations can be used for nutritional assessment in patients on TPN. Plasma 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 plasma. 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

Avoid gel separator tubes
Plasma (K2-EDTA)

Containers

Preferred Containers

BD 6 ml K2-EDTA Royal Blue Vacutainer (Reference # 368381)

Volume

Sample Volume

2 mL

Specimen Comment

Avoid gel separator tubes.

Collection & Handling

Collection Instructions

Collect in contaminant-free tube. Avoid hemolysis.

Handling Information

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

Additional Information

Concentrations of chromiumare higher in erythrocytes than in plasma. The results in plasma maybe 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
    2.5 - 6.0
    µg/L x 19.2

Referral Location

Canada

Test Version

Last Updated

2019-09-30