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Test ID CFRC Bacterial Culture, Cystic Fibrosis, Respiratory

Useful For

Detection of aerobic bacterial pathogens from cystic fibrosis patient specimens

Reflex Tests

Test ID Reporting Name Available Separately Always Performed
COMM Identification Commercial Kit No, (Bill Only) No
RMALD Ident by MALDI-TOF mass spec No, (Bill Only) No
GID Bacteria Identification No, (Bill Only) No
ISAE Aerobe Ident by Sequencing No, (Bill Only) No
REFID Additional Identification Procedure No, (Bill Only) No
SALS Serologic Agglut Method 1 Ident No, (Bill Only) No
EC Serologic Agglut Method 2 Ident No, (Bill Only) No
SHIG Serologic Agglut Method 3 Ident No, (Bill Only) No
STAP Identification Staphylococcus No, (Bill Only) No
STRP Identification Streptococcus No, (Bill Only) No
BLA Beta Lactamase No, (Bill Only) No
KPNRP KPC and NDM PCR Yes, External; No Internal (KPND1 Bill Only) No
HODGE Carbapenamase-Modified Hodge Test Yes, External; No Internal (HODGB Bill Only) No
CARNP Carbapenemase-Carba NP Test Yes, External; No Internal (CARNB Bill Only) No

Testing Algorithm

When this test is ordered, the reflex tests may be performed and charged.

Method Name

Conventional Culture Technique

Reporting Name

Bacterial Culture, Cystic Fibrosis

Specimen Type

Varies

If susceptibilities are desired when this test is ordered, also order ZMMLS / Antimicrobial Susceptibility, Aerobic Bacteria, MIC. Each pathogen isolated will then be tested with the appropriate susceptibility panel. Charges are added for each susceptibility test performed.

 

Forms: If not ordering electronically, complete, print, and send a Microbiology Test Request Form (T244) with the specimen (http://www.mayomedicallaboratories.com/it-mmfiles/microbiology_test_request_form.pdf).

 

Specimen must arrive within 48 hours of collection

 

Specimen source is required.

 

Submit only 1 of the following specimens:

 

Preferred:

Specimen Type: Sputum, expectorated or induced

Container/Tube: Sterile container               

Specimen Volume: Entire collection

 

Acceptable:

Specimen Type: Bronchial aspirate or washing, bronchoalveolar lavage, endotracheal, or tracheal

Container/Tube: Sterile container       

Specimen Volume: Entire collection

 

Specimen Type: Throat swab

Container/Tube: Modified Stuart transport device

Specimen Volume: Entire specimen

Specimen Minimum Volume

2 mL

Specimen Stability Information

Specimen Type Temperature Time
Varies Refrigerated 48 hours

Clinical Information

Life expectancy of patients with cystic fibrosis (CF) has increased steadily over the past 50 years, in large part due to improvements in the management of lung disease in this patient population. Still, chronic lung infection is responsible for 75% to 85% of deaths in patients with CF. Appropriate treatment for the causative organism can reduce morbidity and mortality.

 

The number of microbial species associated with CF lung disease is relatively limited. These include Pseudomonas aeruginosa (mucoid and nonmucoid), Staphylococcus aureus, Burkholderia cepacia complex, Stenotrophomonas maltophilia, other nonfermenting gram-negative rods, Haemophilus influenzae, and Streptococcus pneumoniae. Nontuberculous mycobacteria and Aspergillus species may also play a role in CF lung disease, in addition to common respiratory viruses. This culture, which is specifically designed for CF patients, utilizes conventional and additional selective media (compared to non-CF respiratory cultures) to isolate bacteria commonly associated with pulmonary disease in CF patients.

 

In selected centers, lung transplantation is performed on CF patients. This test is appropriate for lung transplant patients with underlying CF because they can continue to harbor the same types of organisms as they did pretransplantation. CF patients may be colonized or chronically infected by these organisms over a long period of time.

Reference Values

No growth or usual flora

Identification of probable pathogens

Cautions

Some bacterial agents that cause lower respiratory infections (eg, mycobacteria, Legionella species, Mycoplasma pneumoniae) are not detected by this assay and require special procedures. If the bacterial culture is negative, clinicians should consider additional testing to detect other bacterial, viral, or fungal agents.

  

Results must be interpreted in conjunction with clinical findings and previous culture results.

Day(s) Performed

Monday through Sunday; Continuously

Report Available

5 days

Performing Laboratory

Mayo Medical Laboratories in Rochester

Test Classification

This test uses a standard method. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements.

CPT Code Information

87070-Bacteria, culture, cystic fibrosis, respiratory

87077-Identification commercial kit (if appropriate)

87077-Ident by MALDI-TOF mass spec (if appropriate)

87077-Bacteria Identification (if appropriate)

87077-Additional Identification procedure (if appropriate)

87077-Identification Staphylococcus (if appropriate)

87077-Identification Streptococcus (if appropriate)

87147 x 5-Serologic agglut method 1 ident (if appropriate)

87147-Serologic agglut method 2 ident (if appropriate)

87147 x 4-Serologic agglut method 3 ident (if appropriate)

87153-Aerobe Ident by sequencing (if appropriate)

87185-Beta lactamase (if appropriate)

87185-Carbapenemase detection, Carba NP test (if appropriate)

87185-Carbapenemase detection, modified Hodge test (if appropriate)

87798 x 2-KPC and NDM PCR (if appropriate)

NY State Approved

Yes