Thiocyanate Quantitative, Serum or Plasma
Also known as: THIOCY SP
Use
The Thiocyanate Quantitative test is used for therapeutic monitoring in patients receiving sodium nitroprusside therapy and for screening for thiocyanate poisoning. Monitoring thiocyanate levels is essential for preventing toxicity and ensuring proper therapeutic levels in clinical settings.
Special Instructions
The test is not performed at ARUP; therefore, separate specimens must be submitted when multiple tests are ordered. Ensure timely separation from cells within 2 hours of collection and proper storage conditions to maintain sample integrity.
Limitations
This test has not been cleared or approved by the US Food and Drug Administration (FDA). It is important to note that quantitative analysis is highly dependent on proper handling and storage of the specimen, as well as the testing methodologies used by external laboratories.
New York Approved
Methodology
Mass Spectrometry
Biomarkers
LOINC Codes
- 3002-3
Result Turnaround Time
10-14 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
1 mL
Minimum Volume
0.3 mL
Container
ARUP standard transport tube
Collection Instructions
Plain red, lavender (K2 or K3EDTA), or pink (K2EDTA).
Storage Instructions
Refrigerated. Also acceptable: Room temperature or frozen.
Causes for Rejection
Separator tubes.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 1 month |
| Refrigerated | 1 month |
| Frozen | 1 month |