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Test Code VIT D VITAMIN D, 25-HYDROXY

Methodology

Competitive Chemiluminescence Immunoassay (CLIA)

Specimen Requirements

Specimen Type: Serum

Container/Tube: Red top or serum gel

Specimen Volume: 0.50 mL

Specimen Minimum Volume: 0.50 mL

 

Specimen Stability

2 to 8° C - 5 days

Day(s) Test Set Up

Monday through Friday

Maximum Laboratory Time

Monday to Friday: 8 to 24 hours

Saturday and Sunday: 48 hours

Specimen Transport Temperature

Refrigerated OK

Frozen OK

Ambient NO

Reference Values

TOTAL 25-HYDROXYVITAMIN D2 AND D3 (25-OH-VitD)

  • ≤20 ng/mL (Deficiency)*
  • 21-29 ng/mL (Insufficiency)**
  • 30-80 ng/mL (Optimum levels)***
  • >100 ng/mL (Toxicity possible)****

*Could be associated with osteomalacia or rickets

**May be associated with increased risk of osteoporosis or secondary hyperparathyroidism

***Optimum levels in the normal population

****100 ng/mL is the lowest reported level associated with toxicity in patients without primary hyperparathyroidism who have normal renal function. Most patients with toxicity have levels >150 ng/mL. Patients with renal failure can have very high 25-OH-VitD levels without any signs of toxicity, as renal conversion to the active hormone 1,25-OH-VitD is impaired or absent.

 

These reference ranges represent clinical decision values that apply to males and females of all ages, rather than population-based reference values. Population reference ranges for 25-OH-VitD vary widely depending on ethnic background, age, geographic location of the studied populations, and the sampling-season. Population-based ranges correlate poorly with serum 25-OH-VitD concentrations that are associated with biologically and clinically relevant vitamin D effects and are therefore of limited clinical value.

 

Limitations:

 

Bilirubin-40 mg/dL

Hemoglobin-200 mg/dL

Cholesterol-300mg/dL

Triglycerides-589mg/dL

 

Performing Laboratory

Logan Health Medical Center Laboratory

Test Classification and CPT Coding

CPT Code:

82306