Babesia Species by PCR
2008665
Ordering Recommendation
 
Mnemonic
BABPCR
Methodology
Qualitative Polymerase Chain Reaction
Performed
Sun-Sat
Reported
1-3 days  
New York DOH Approval Status
This test is New York DOH approved.
Submit With Order
Specimen Required
Patient Preparation
  
Collect
Lavender (EDTA) or pink (K2EDTA).  
Specimen Preparation
Transport 1 mL whole blood. (Min: 0.6 mL)  
Storage/Transport Temperature
Refrigerated.  
Unacceptable Conditions
Heparinized specimens.  
Remarks
  
Stability
Ambient: 24 hours; Refrigerated: 1 week; Frozen: 30 days  
Reference Interval
   
Interpretive Data
A negative result does not rule out the presence of PCR inhibitors in the patient specimen or test-specific nucleic acid in concentrations below the level of detection by this test.

See Compliance Statement B: www.aruplab.com/CS
Statement B: This test was developed and its performance characteristics determined by ARUP Laboratories. The U.S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions.
 
Note
This test detects and speciates B. microti. The nucleic acid from B. duncani, B. divergens, strain MO-1, and strain EU-1 will be detected by this test but cannot be differentiated.
CPT Code(s)
87798 x2
Components
Component Test Code*Component Chart NameLOINC
2008666Babesia species by PCR42641-1
2008668Babesia microti by PCR47396-7
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
Aliases