Ordering Recommendation
Nonspecific indicator of muscle inflammation or damage.
Mnemonic
CK
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
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
N/A
CPT Codes
82550
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