Test Code CRP C-Reactive Protein
Specimen and Container/Tube
Specimen Type: Plasma
Preferred Specimen: Li-Heparin Mint Green Top
Other Acceptable specimens: Serum/Gold Top, Serum/Red Top, Plasma/Lavendar K2 Top, Plasma/Lavendar K3 Top
Specimen Handling and Transport Instructions
UCMC Onsite Instructions:
Collect specimen per standard collection procedure and send to laboratory immediately.
UCMC Offsite and UC MedLab Outreach Instructions:
- Samples should be centrifuged within 2 hours of collection.
- Centrifuge specimens at >2500 x g for 10 minutes at room temperature.
- Aliquot sample into plastic transport tube containing a minimum of 0.2 mL of specimen.
- Li-Heparin Plasma and Serum samples must be sent room temperature at 15-25oC.
- For K2 and K3 plasma, samples must be sent referigerated at 2-8oC.
Rejection Criteria
- Common specimen rejected situations include: incorrect specimen type, insufficient volume, missing or incomplete specimen identifiers, incorrect specimen transport, or specimens outside stability limits.
- Specimens that are clotted or grossly hemolyzed.
- Specimens that were transported unspun/whole blood and draw time is greater than 6 hours.
Reference Values
Test |
Age |
Sex |
Reference Range |
CRP |
All |
All |
<5 mg/L |
Note: Reference range based on in-house studies, on the recommendations from Tietz Textbook of Clinical Chemistry and Roche Diagnostics product literature.
Critical Values
Analyte |
Unit |
Low |
High |
Age |
N/A |
N/A |
N/A |
N/A |
N/A |
CPT Codes
86140
LOINC Codes
1988-5
Volume
Preferred Volume: 0.5 mL
Minimum Volume: 0.2 mL
Specimen Stability
Storage Temperature |
Stability for Li-Heparin Plasma and Serum |
Room temperature |
2 weeks |
Refrigerated |
3 weeks |
Frozen |
12 months |
Storage Temperature |
Stability for K2 and K3 Plasma |
Room temperature |
24 hours |
Refrigerated |
3 weeks |
Frozen |
12 months |
Collection Instructions
Collect specimen per standard laboratory collection procedures.
Test Components
C-Reactive Protein
Clinical Indications
CRP assays are used to detect systemic inflammatory processes; to assess treatment of bacterial infections with antibiotics; to detect intrauterine infections with concomitant premature amniorrhexis; to differentiate between active and inactive forms of disease with concurrent infection; to determine the presence of post-operative complications at an early stage, such as infected wounds.
Methodology
Particle Enhanced Immunoturbidimetric Assay (Roche Diagnostics)
Additional Information
- Results should always be assessed in conjunction with patient's medical history, clinical examination and other findings.
- High dose hook-effect: No false result occurs up to a CRP concentration of 1200 mg/L.
- Ticarcillin causes no significant interference up to 225 mg/L.
- CRP response may be less pronounced in patients suffereing from liver disease.
- Postoperative monitoring of CRP level of patients can aid in the recognition of unexpected complications (persisting high or increasing levels. Measuring changes in the concentration of CRP provides useful diagnostic information about how acute and how serious a disease is. It also allows judgements about the disase genesis. Persistence of high serum CRP concentrations is usually a grave prognostic sign which generally indicates the presence of an uncontrolled infection.
Turnaround Time
Turnaround times are relative to the time the specimen is received in the test laboratory.
STAT Turnaround Time: 1 hour
Routine Turnaround Time: 4 hours
Testing Schedule: 24/7
Synonyms/Keyword Search
Protein, C-Reactive
Last Review Date
8/19/2024