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Test Code MISC2MAYOFL Fluoride, Plasma

Reporting Name

Fluoride, P

Useful For

Assessing accidental fluoride ingestion

 

Monitoring patients receiving sodium fluoride for bone disease or patients receiving voriconazole therapy

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Specimen Type

Plasma Heparin


Specimen Required


Supplies: Sarstedt Aliquot Tube, 5 mL (T914)

Collection Container/Tube: Green top (sodium heparin)

Submission Container/Tube: Plastic vial

Specimen Volume: 3 mL

Collection Instructions: Centrifuge and aliquot plasma into a plastic vial. Glass tubes are not acceptable.


Specimen Minimum Volume

1.2 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Plasma Heparin Refrigerated (preferred) 14 days
  Ambient  14 days
  Frozen  14 days

Reference Values

<4.1 mcmol/L

Day(s) Performed

Tuesday

Test Classification

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information

82735

LOINC Code Information

Test ID Test Order Name Order LOINC Value
FL Fluoride, P 14726-4

 

Result ID Test Result Name Result LOINC Value
8641 Fluoride, P 14726-4

Clinical Information

Fluoride induces bone formation by stimulating osteoblasts. Because fluorides increase bone density, they are used in dental preparations and as an antiosteoporotic agent. However, prolonged high exposure to fluoride produces changes in bone morphology consistent with osteomalacia, including prolonged mineralization lag time and increased osteoid thickness. The adverse skeletal effects of fluoride are associated with plasma fluoride greater than 4 mcmol/L. Chronic fluorosis may produce osteosclerosis, periostitis, calcification of ligaments and tendons, and crippling deformities.

 

Prolonged exposure to the fluoride-containing antifungal agent voriconazole can produce high plasma fluoride concentrations and bone changes (periostitis). Several other medicines also contain fluoride are used for treating skin diseases (eg, flucytosine, an antifungal) and some cancers (eg, fluorouracil, an antimetabolite).

Interpretation

Humans exposed to fluoride-treated water typically have plasma fluoride in the range of 1 to 4 mcmol/L. Those who are not drinking fluoride-treated water have plasma fluoride less than 1 mcmol/L. Plasma fluoride values greater than 4 mcmol/L indicate excessive exposure and are associated with periostitis.

Method Description

The fluoride electrode consists of a single-crystal lanthanum fluoride membrane and an internal reference bonded into an epoxy body. The crystal is an ionic conductor in which only fluoride ions are mobile. When the membrane is in contact with a fluoride solution, potential develops across the membrane. This potential depends on the level of free fluoride ions in solution and is measured against an external constant reference potential with a digital pH/mV meter.(Instruction manual: Fluoride Ion Selective Electrode User Guide. Thermo Scientific; 09/2016)

Report Available

2 to 8 days

Reject Due To

Gross hemolysis OK
Gross lipemia OK
Gross icterus OK

Method Name

Ion-Selective Electrode (ISE)

Secondary ID

8641