Fluoride Quantitative, Serum or Plasma

0091341
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Example Reports
Detected
None Detected
Ordering Recommendation
Mnemonic
FLUORIDE
Methodology

Quantitative Ion-Specific Electrode

Performed

Varies

Reported

7-10 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
N/A
CPT Codes

82735

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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)