Barium Quantitative, Serum or Plasma
Also known as: BARIUM SP
Use
The Barium Quantitative, Serum or Plasma test is a diagnostic tool used for the detection and quantification of barium levels in the serum or plasma of a patient. It is essential in cases of suspected barium exposure or poisoning, as barium is a toxic metal. The quantitative analysis aids in monitoring and managing the patient's exposure levels, guiding clinical decisions for treatment and management of toxicity symptoms.
Special Instructions
Not provided.
Limitations
The test has not been cleared or approved by the US Food and Drug Administration. Certain collection tubes may artifactually increase measured barium concentrations, which can complicate the interpretation of results. Elevated results may also result from environmental contamination at the time of specimen collection. It is recommended to verify unexpected elevated results by retesting with a new specimen collected in a trace metal-free container.
New York Approved
Methodology
Mass Spectrometry
Biomarkers
Barium
Analyte
LOINC Codes
- 5589-7 - Barium SerPl-mCnc
Result Turnaround Time
5-8 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
1 mL
Minimum Volume
0.4 mL
Container
Acid-washed transfer vial or ARUP trace element-free transport tube
Collection Instructions
Separate from cells ASAP or within 2 hours of collection. Use certified metal-free containers.
Storage Instructions
Refrigerated. Also acceptable: Room temperature or frozen.
Causes for Rejection
Polymer gel separation tube (SST or PST).
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 1 month |
| Refrigerated | 1 month |
| Frozen | 1 month |
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