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 Plasma
Collection Instructions:
1. Within 2 hours of collection, centrifuge the specimen.
2. For plasma gel tubes, plasma may sit on gel or be aliquoted into a plastic vial.
3. For green top tubes, aliquot plasma immediately into a plastic vial.
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
Plasma: 0.25 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| 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