Cystic Fibrosis Respiratory Culture

Test Code
CXCFR


Includes

Gram stain and Aerobic culture for bacterial respiratory pathogens from patients with Cystic Fibrosis




Preferred Specimen

Submit only 1 of the following specimens:

Specimen Type: Sputum (expectorated, induced, suctioned)
Collection Container: Sterile container
Specimen Volume: 2 mL




Other Acceptable Specimens
Specimen Type: BAL, bronchial brushings, endotracheal aspirate
Collection Container: Sterile container
Specimen Volume: 2 mL

Specimen Type: Throat
Collection Container: E-Swab
Specimen Volume: Swab


Instructions

Sputum, Expectorated

  1. Patient should rinse mouth and gargle with sterile water prior to collection.
  2. Instruct the patient NOT to expectorate saliva or postnasal discharge into the container.
  3. Collect expectorated sputum into a sterile container with a screw cap


Sputum, Induced

  1. Using a wet toothbrush and sterile water or saline, brush the buccal mucosa, tongue, and gums for 5 to 10 minutes prior to the procedure.
  2. Rinse the patients mouth with sterile water or saline.
  3. Using an ultrasonic nebulizer, have the patient inhale approximately 20-30ml of 3% NaCl.
  4. Collect inducted sputum specimens into a sterile container with a screw cap


Endotracheal aspirate

  1. Aspirate the specimen into a sterile sputum trap (i.e., Luken trap) and aseptically transfer the sputum sample to a sterile screw-cap container with the cap tightly secured before transport.


Bronchial Wash, Transbronchial Biopsy, Bronchoalveolar lavage (BAL), Bronchial Brushing

  1. Follow standard collection practices


Specimen Stability
Must be received within 24 hrs of collection.


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Rejection will occur for the following reasons: improperly labeled specimen, insufficient volume, specimen not submitted in appropriate transport container, samples submitted in formalin, frozen samples submitted.


Methodology
Bacterial culture, organism identification and antibiotic susceptibility testing as appropriate for specimen source


Setup Schedule
Daily


Report Available

Negative or normal flora report is final at 5 days. Positive report depends on the extent of organism workup.




Limitations

This culture method is not acceptable for detection of Legionella species, Bordetella pertussis, Mycoplasma pneumoniae, or Chlamydophila pneumoniae. Contact the laboratory if detection of these pathogens is required. If a quantitative BAL is required, it must be selected as a source or submitted as a separate order (Culture, Respiratory/BAL Quantitative).




Reference Range
Negative for Pathogens or Growth of Normal Respiratory Flora


Clinical Significance
Diagnosis of lower respiratory tract infection may be complicated by the contamination of specimens with upper respiratory tract flora during collection. Upper respiratory flora may include colonizing organisms that are not responsible for infection. The presence of low quantity potentially pathogenic organisms mixed with normal flora should be integrated into the clinical picture for interpretation of significance.


Performing Laboratory

Inova Laboratories

2832 Juniper Street

Fairfax, VA 22031




Last Updated: May 11, 2023
Last Review: N. Wolford, May 11, 2023


The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.