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Test ID KDBAL Karius Focus, Bronchoalveolar Lavage


Ordering Guidance


Order this test when shipping specimens directly to Karius. However, approval is required prior to ordering due to limited availability at this time. Contact Mayo Clinic Laboratories at 800-533-1710.



Specimen Required


Supplies: Karius KDBAL Kit (T1015)

Container/Tube: Streck CP tube

Specimen Volume: 1 mL

Collection Instructions:

1. Collect bronchoalveolar lavage fluid (BALF) specimen according to your institutional guidelines.

2. Within 12 hours of specimen collection, transfer at least 1 mL of BALF specimen to the Streck CP tube using disposable sterile pipette, taking care to avoid spilling storage reagent in Streck CP tube.

3. Screw the cap tightly and gently invert the tube 8-10 times.

4. Do Not freeze the Streck CP tube.

5. See Karius Focus: BAL Specimen Collection and Preparation Process for complete instructions.

Additional Information:

1. Specimen cannot be shared with other tests.

2. Specimen trap collection containers (with suction catheters attached) will be rejected due to the high risk of leakage and contamination upon opening. Avoid use of these for BALF specimens.


Useful For

Detection of microbial cell-free DNA from over 500 bacteria, fungi, parasites, and DNA viruses known to cause lung infections in bronchoalveolar lavage fluid

Testing Algorithm

For information regarding when to order the Karius Spectrum test or diagnostic algorithms, see Considerations for the Implementation of the Karius Spectrum and Karius Focus BAL Tests.

Method Name

Metagenomic Sequencing

Reporting Name

Karius Focus Direct, BAL

Specimen Type

Bronchoalveolar Lavage

Specimen Minimum Volume

See Specimen Required

Specimen Stability Information

Specimen Type Temperature Time
Bronchoalveolar Lavage Ambient 7 days

Reference Values

An interpretive report will be provided.

Day(s) Performed

Monday through Saturday

Report Available

3 to 5 days

Performing Laboratory

KARIUS LABORATORY DIRECT SHIP

Test Classification

The Karius Focus: BAL test was developed and its performance characteristics determined by Karius. The Karius laboratory is certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA '88) and is accredited by the College of American Pathologists (CAP) to perform high-complexity laboratory testing. This test has not been reviewed or cleared by the US Food and Drug Administration.

CPT Code Information

87999

LOINC Code Information

Test ID Test Order Name Order LOINC Value
KDBAL Karius Focus Direct, BAL Not Provided

 

Result ID Test Result Name Result LOINC Value
KDBAL Karius Focus Direct, BAL Not Provided