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Fluoride Quantitative, Serum or Plasma
0091341
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Ordering Recommendation
Mnemonic
FLUORIDE
Methodology
Quantitative Ion-Specific Electrode
Performed
Varies
Reported
8-11 days
New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
Collect
Plain Red, Lavender (EDTA) or Pink (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 separator tubes.
Remarks
Stability
Ambient: 1 month; Refrigerated: 1 month; Frozen: 28 months
Reference Interval
By report
Interpretive Data
Compliance Category
Performed by non-ARUP Laboratory
Note
Hotline History
Hotline History
Date of Change
Test Name Change
Methodology
Performance/Reported Schedule
Specimen Requirements
Reference Interval
Interpretive Data
Note
CPT Code
Component Change
Other Interface Change
New Test
Inactive
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
- F
Fluoride Quantitative, Serum or Plasma
National Medical Services (NMS)
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