Bartonella Species by PCR
Also known as: BART DNA
Use
This test is designed to detect Bartonella species in various specimen types including blood, cerebrospinal fluid (CSF), or tissue. It is used to identify the presence of Bartonella infections which can lead to conditions such as Cat Scratch Disease and other bartonellosis. The detection is achieved using qualitative Polymerase Chain Reaction (PCR), which is a sensitive method to identify Bartonella DNA in clinical specimens.
Special Instructions
It is important for the specimen source to be specified as this can affect the test processing and results. Specimens should be collected and handled according to the specified guidelines to ensure accuracy and reliability of the test results.
Limitations
This test, while highly specific and sensitive, may not detect Bartonella DNA in all infected cases, especially if the bacterial load is below the detection threshold. The presence of PCR inhibitors in the specimen may also lead to false negatives. The test has not been cleared or approved by the FDA but is performed in a CLIA certified lab for clinical purposes.
New York Approved
Methodology
PCR-based (Qualitative Polymerase Chain Reaction)
Biomarkers
LOINC Codes
- 31208-2
- 48864-3
Result Turnaround Time
1-5 days
Related Documents
For more information, please review the documents below
Specimen
Whole Blood
Volume
1 mL
Minimum Volume
0.5 mL
Container
Lavender (EDTA), pink (K2EDTA) or serum separator tube. Also acceptable: CSF or tissue.
Storage Instructions
Whole blood: Refrigerated. FFPE: Room temperature. All others: Frozen.
Causes for Rejection
Heparinized specimens, tissues in optimal cutting temperature compound.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 7 days |
| Refrigerated | 7 days |
| Frozen | 7 days |