Test Code BVRNA Bacterial Vaginosis, Nucleic Acid Amplification, Vaginal
Specimen Required
Specimen Type: Vaginal
Supplies: Aptima Multitest Swab Collection Kit (T584)
Container/Tube: Aptima Multitest Swab
Specimen Volume: Swab
Collection Instructions:
1. Specimen must be collected using the Aptima Multitest Swab Collection Kit.
2. Insert swab (pink shaft) about 5 cm past introitus and rotate gently for 30 seconds.
3. Place swab into transport tube provided in collection kit. Snap off swab at score line so swab fits into closed tube.
4. Cap tube securely, and label tube with patient's entire name and collection date and time.
5. Maintain swab container between 2 and 30° C (refrigerate temperature is preferred) and transport within 30 days of collection. If longer storage is needed, store frozen between -20 and -70° C for up to 60 days.
Useful For
Aid for diagnosis of bacterial vaginosis
This test is not intended for use in medico-legal applications.
Method Name
Transcription Mediated Amplification
Reporting Name
Bacterial Vaginosis, Amplified RNASpecimen Type
VaginalSpecimen Minimum Volume
See Specimen Required
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Vaginal | Refrigerated (preferred) | 30 days | APTIMA VIAL |
Frozen | 60 days | APTIMA VIAL | |
Ambient | 30 days | APTIMA VIAL |
Reject Due To
Incorrect swab Transport tube containing more than one swab |
Reject |
Reference Values
Negative
Interpretation
Positive: Results should be interpreted alongside clinical presentation. Up to 40% of asymptomatic patients may test positive by this assay. Assay result is based on relative amounts of Lactobacillus (Lactobacillus gasseri, Lactobacillus crispatus, Lactobacillus jensenii), Gardnerella vaginalis, and Atopobium vaginae. Individual organisms are not reported.
Negative: A negative result does not exclude infection. Assay result is based on relative amounts of Lactobacillus (L gasseri, L crispatus, L jensenii), G vaginalis, and A vaginae.
Inconclusive: Repeat testing on a new sample is recommended if clinically indicated.
Day(s) Performed
Monday through Sunday
Report Available
1 to 4 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
81513
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
BVRNA | Bacterial Vaginosis, Amplified RNA | 103590-6 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
620738 | Bacterial Vaginosis, Amplified RNA | 103590-6 |