Alkaline Phosphatase, Serum or Plasma

0020005
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Example Reports
Abnormal
Normal
Ordering Recommendation

Aid in the investigation of hepatobiliary and bone disease.

Mnemonic
ALKP
Methodology

Quantitative Enzymatic

Performed

Sun-Sat

Reported

Within 24 hours

New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
Collect

Plasma separator tube or serum separator tube.

Specimen Preparation

Allow serum tube to clot completely at room temperature. Separate serum or plasma from cells within 2 hours of collection. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.2 mL)

Storage/Transport Temperature

Refrigerated.

Unacceptable Conditions

Specimens collected in EDTA or sodium fluoride/potassium oxalate. Grossly hemolyzed specimens.

Remarks
Stability

After separation from cells: Ambient: 1 week; Refrigerated: 1 week; Frozen: 2 months

Reference Interval

By report (reports may vary based on instrumentation)

Interpretive Data



Compliance Category

FDA

Note
Hotline History
N/A
CPT Codes

84075

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Components
Component Test Code* Component Chart Name LOINC
0020005 Alkaline Phosphatase 6768-6
* 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
  • ALK PHOS
  • Alkaline Phosphatase
  • Alkp
Alkaline Phosphatase, Serum or Plasma