Test Code CKP Creatine Kinase (CK), Plasma
Necessary Information
Patient's age and sex are required.
Specimen Required
Collection Container/Tube:
Preferred: Light-green top (lithium heparin plasma gel)
Acceptable: Green top (lithium heparin)
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions:
1. Gel tubes should be centrifuged within 2 hours of collection.
2. Green-top tubes should be centrifuged, and the plasma 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 using plasma specimens
Method Name
Photometric
Reporting Name
Creatine Kinase, PSpecimen Type
Plasma Li HeparinSpecimen Minimum Volume
0.25 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Plasma Li Heparin | 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 younger 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
Performing Laboratory
MCHS- MankatoTest 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 |
---|---|---|
CKP | Creatine Kinase, P | 2157-6 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
CKP | Creatine Kinase, P | 2157-6 |