Home
HelpTest ID BPRPV Bordetella pertussis and Bordetella parapertussis, Molecular Detection, PCR, Varies
Necessary Information
Specimen source is required.
Specimen Required
The high sensitivity of amplification by polymerase chain reaction (PCR) requires the specimen to be processed in an environment in which contamination of the specimen by Bordetella pertussis or Bordetella parapertussis DNA is unlikely.
Submit only 1 of the following specimens:
Preferred:
Specimen Type: Nasopharyngeal swab
Supplies:
Culture Swab - Liquid Stuarts/Single Swab (NP Swab) (T515)
Container/Tube: Rayon swab with an aluminum shaft placed in transport medium such as a green-top nasopharyngeal swab (rayon mini-tip) with Stuart's media (no charcoal), or Stuart's media with charcoal, or Amies media with or without charcoal (Transwab Nasopharyngeal with Charcoal System).
Additional Information:
1. Swab transport containers without charcoal must contain a pledget saturated with either Stuart's or Amies liquid media. Clear semi-solid/solid media is gel and will be rejected.
2. Other swab or media types may be inhibitory to PCR testing and will be rejected.
Acceptable:
Specimen Type: Nasopharyngeal (not throat) aspirate/wash or nasal aspirate/wash
Container/Tube: Sterile container with a screw top cap (no transport media)
Specimen Volume: Entire collection
Useful For
Preferred diagnostic test for the detection of Bordetella pertussis or Bordetella parapertussis
This test is not recommended for screening asymptomatic individuals who may carry B pertussis or parapertussis.
This test is not recommended for follow up of patients previously diagnosed with pertussis (ie, as a test of cure).
Method Name
Polymerase Chain Reaction (PCR)/DNA Probe Hybridization
Reporting Name
Bordetella, PCR, VariesSpecimen Type
VariesSpecimen Minimum Volume
0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Varies | Refrigerated (preferred) | 7 days | |
| Ambient | 7 days | ||
| Frozen | 7 days |
Reference Values
Not applicable
Day(s) Performed
Monday through Friday, Sunday
Report Available
1 to 3 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
87798 x 2
87798 (if appropriate for government payers)
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| BPRPV | Bordetella, PCR, Varies | 90441-7 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| BPRS | Specimen source | 31208-2 |
| 618312 | Bordetella pertussis PCR | 43913-3 |
| 618313 | Bordetella parapertussis PCR | 42588-4 |
Forms
If not ordering electronically, complete, print, and send a Microbiology Test Request (T244) with the specimen.