Test Code CRPP C-Reactive Protein, Plasma
Ordering Guidance
To assess the risk of cardiovascular disease or events using C-reactive protein, order HSCRP / C-Reactive Protein, High Sensitivity, Serum.
Necessary Information
Indicate patient's age and sex.
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: 0.5 mL
Collection Instructions:
1. Plasma gel tube should be centrifuged within 2 hours of collection.
2. Green-top tube should be centrifuged, and the plasma aliquoted into a plastic vial within 2 hours of collection.
Useful For
Detecting systemic inflammatory processes
Detecting infection and assessing response to antibiotic treatment of bacterial infections
Differentiating between active and inactive disease forms with concurrent infection
Reporting Name
C-Reactive Protein (CRP), PSpecimen Type
Plasma Li HeparinSpecimen Minimum Volume
0.25 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Plasma Li Heparin | Refrigerated (preferred) | 21 days | |
Frozen | 365 days | ||
Ambient | 14 days |
Reject Due To
Gross hemolysis | Reject |
Reference Values
≤5.0 mg/L
Reference values apply to all ages.
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
86140
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
CRPP | C-Reactive Protein (CRP), P | 1988-5 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
CRPP | C-Reactive Protein (CRP), P | 1988-5 |
Method Name
Immunoturbidimetric assay