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0091341
Fluoride Quantitative, Serum or Plasma
FLUORIDE
Ordering Recommendation
New York DOH Approval Status
This test is New York state approved.
Specimen Required
Patient Preparation
Collect
Plain red or lavender (K2EDTA)
Specimen Preparation
Separate from cells ASAP or within 2 hours of collection. Transfer 2 mL serum or plasma to an ARUP standard transport tube. (Min: 0.6 mL)
Test is not performed at ARUP; separate specimens must be submitted when multiple tests are ordered.
Storage/Transport Temperature
Refrigerated. Also acceptable: Room temperature or frozen.
Unacceptable Conditions
Gray (potassium oxalate/sodium fluoride) or polymer gel separation tube (SST or PST).
Remarks
Stability
Ambient: 1 month; Refrigerated: 1 month; Frozen: 28 months
Methodology
Quantitative Ion-Selective Electrode
Performed
Varies
Reported
8-11 days
Reference Interval
By report
Interpretive Data
Compliance Category
Performed by non-ARUP Laboratory
Note
Hotline History
N/A
CPT Codes
82735
Components
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 0091340 | Fluoride Quantitative, Serum or Plasma | 5649-9 |
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
Aliases
Fluoride Quantitative, Serum or Plasma
National Medical Services (NMS)
