Ordering Recommendation

CDC-recommended test for the diagnosis of pertussis.

Mnemonic
BORD PCR
Methodology

Qualitative Polymerase Chain Reaction

Performed

Sun-Sat

Reported

2-7 days

New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
Collect

Respiratory specimen: Aspirate, bronchoalveolar lavage (BAL), swab or sputum.

Specimen Preparation

Fluid: Transfer 2 mL respiratory specimen to a sterile container. (Min: 0.5 mL) Also acceptable: Transfer to viral transport media (ARUP supply #12884). Available online through eSupply using ARUP Connect™ or contact ARUP Client Services at (800) 522-2787
Swabs: Place in viral transport media.

Storage/Transport Temperature

Frozen

Unacceptable Conditions

Calcium-alginate swabs.

Remarks

Specimen source required.

Stability

Ambient: 24 hours; Refrigerated: 5 days; Frozen: 2 weeks.

Reference Interval
Interpretive Data



Compliance Category

Laboratory Developed Test (LDT)

Note
Hotline History
N/A
CPT Codes

87798

Components
Component Test Code* Component Chart Name LOINC
0065078 Bordetella pertussis by PCR 23826-1
0065079 Bordetella parapertussis by PCR 29723-4
2002176 B. pertussis/parapertussis Source 31208-2
* 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
  • Bordetella pertussis and parapertussis
  • Bordetella Pertussis, parapertussis Molecular Detection
  • Whooping Cough
Bordetella pertussis/parapertussis by PCR