Test Code CK Creatine Kinase (CK), Serum
Necessary Information
Patient's age and sex are required.
Specimen Required
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions:
1. Serum gel tubes should be centrifuged within 2 hours of collection.
2. Red-top tubes should be centrifuged, and the serum aliquoted into a plastic vial within 2 hours of collection.
Useful For
Diagnosing and monitoring myopathies or other trauma, toxin, or drug-induced muscle injury
Method Name
Photometric, Creatine Phosphate + ADP
Reporting Name
Creatine Kinase (CK), SSpecimen Type
SerumSpecimen Minimum Volume
0.25 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Refrigerated (preferred) | 7 days | |
Frozen | 28 days | ||
Ambient | 48 hours |
Reject Due To
Gross hemolysis | Reject |
Reference Values
Males
≤3 months: not established
>3 months: 39-308 U/L
Females
≤3 months: not established
>3 months: 26-192 U/L
Reference values have not been established for patients that are less than 3 months of age.
Note: Strenuous exercise or intramuscular injections may cause transient elevation of creatine kinase (CK).
Day(s) Performed
Monday through Sunday
Report Available
Same day/1 to 2 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
82550
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
CK | Creatine Kinase (CK), S | 2157-6 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
CK | Creatine Kinase (CK), S | 2157-6 |