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Test Code CRPHS CRP, High Sensitivity (CHD Risk)

Useful For

This test is useful for assessing atherosclerosis/cardiovascular risk in apparently healthy adults. Because CRP is an acute phase reactant and shows significant elevations in inflammatory states, this test should not be used for acutely ill patients. It is essential that the patient be in a stable, basal state prior to assessment. Repeat testing may be required to confirm a basal CRP level. For evaluating inflammatory states, the routine CRP assay should be used which is available on a 24-hour basis.

Synonyms/Keywords

CRP, High Sensitivity C-Reactive Protein, Ultrasensitive CRP

Specimen Requirements

Fasting Required Specimen Type Preferred Container/Tube Acceptable Container/Tube Specimen Volume Specimen Minimum Volume
(allows for 1 repeat)
Pediatric Minimum Volume
(no repeat)
No Serum Red Top Tube (RTT) Serum Separator Tube (SST) 0.5 mL 0.4 mL 0.3 mL

Collection/Processing Instructions

Samples should be centrifuged and serum removed within two hours of collection. 

Repeated freeze/thaw cycles should be avoided.  Specimens that are very lipemic (3+) or that are turbid from freezing need to be clarified by centrifuging for 10 minutes at approximately 15,000 x g prior to testing. 

Specimen Stability Information

Specimen Type Temperature Time
Serum Refrigerate 7 days
Frozen 3 months

Rejection Criteria

Plasma samples

Interferences

In very rare cases gammopathy, especially monoclonal IgM (Waldenstroms macroglobulinemia), may cause unreliable results.
Samples containing heterophilic antibodies can cause falsely elevated results. Please note that oral contraceptives have been reported to affect results.

Interpretations

C-Reactive Protein (CRP) has long been used as a sensitive marker of acute inflammation. More recent studies suggest however that subtle changes in CRP levels within the traditional normal range are indicative of inflammatory processes that may play a role in the atherosclerotic plaque formation. Assays capable of measuring these low levels are referred to as "high-sensitivity CRP". These batch assays generally provide an order of magnitude greater sensitivity enabling two decimal place reporting within the normal range of 0 - 1 mg/dL, compared to the routine rapid-turnaround assays for large acute changes in the 0 - 15 mg/dL range.  

 

C-Reactive Protein is an acute phase reactant. Elevated results (>10.0 mg/L by the high-sensitivity assay) may suggest an inflammatory condition and should be repeated after a minimum of several weeks to assure that the patient is in a basal condition.

Reference Range Information

Performing Location Reference Range
Marshfield

Currently, units are in mg/L and cutoffs are per the CDC/AHA consensus Guidelines published in Circulation 2003 (Jan 28); 107:499-511.  

 

<1.0 mg/L: Low Cardiovascular Risk

1.0-3.0 mg/L: Average Risk

>3.0 mg/L: High Risk (2 fold higher than low risk group)

>10.0 mg/L: Suggests inflammation (repeat when basal)

Marshfield Labs Performing Department

Marshfield Labs Chemistry

Performing Information

Performing Location Day(s) Test Performed Analytical Time Methodology/Instrumentation
Marshfield

Monday through Friday at 0900

 

Samples received in the laboratory section after 0900 will be run on the next business day.

6-8 hours Turbidimetric method/Beckman AU680

CPT Codes

CPT Modifier
(if needed)
Quantity Description Comments
86141        

Outreach CPT Codes

CPT Modifier
(if needed)
Quantity Description Comments
86141        

Ordering Applications

Ordering Application Description
Cerner CRP, High Sensitivity (CHD RISK)