0020010
print

Creatine Kinase, Total, Serum or Plasma

CK
Example Reports
Abnormal
Normal

Ordering Recommendation

Nonspecific indicator of muscle inflammation or damage.

Methodology

Quantitative Enzymatic Assay

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 specimen to clot completely at room temperature.  Separate serum or plasma from cells ASAP. 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 potassium oxalate or sodium fluoride. Grossly hemolyzed specimens.

Remarks
Stability

After separation from cells: Ambient: 48 hours; Refrigerated: 1 week; Frozen: 1 month

Reference Interval

Effective February 22, 2022
By Report (reports may vary based on instrumentation)

Interpretive Data



Compliance Category

FDA

Note

Hotline History

View 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
02/22/2022
X
N/A

CPT Codes

82550

Are you an ARUP Client? Click here for your pricing.

Components

Component Test Code* Component Chart Name LOINC
0020010 Creatine Kinase, Total, Ser/Pla 2157-6
* 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

  • CK
  • CK concentation
  • CK level
  • CPK
  • Creatine Phosphokinase
  • phospho-creatine kinase
  • Total CK
Creatine Kinase, Total, Serum or Plasma