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Back to Test Catalogue
Test ID: HBIS P

Bismuth, Plasma

Test Overview

Clinical Utility

Whole blood is the recommended specimen for assessment of bismuth status.

Method

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

Result Included

Bismuth

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 to polypropylene vial. Store and send cold.

Additional Information

Concentrations of bismuth are much higher in erythrocytes than in plasma. The results in plasma 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. Bismuth
    nmol/L
    0.00 - 0.32
    µg/L x 4.785

Referral Location

Canada

Test Version

Last Updated

2019-09-30