Mycoplasma genitalium, NAA, Swab With Reflex to Macrolide Resistance Testing
Use
The test is used to detect the presence of Mycoplasma genitalium in genital-based swab collections. If M. genitalium is detected, further testing for the presence of macrolide resistance will be performed.
Special Instructions
If reflex testing is performed, additional charges/CPT codes may apply. The Aptima® Multitest Swab Specimen Collection Kit is preferred but the Aptima® Unisex Swab Specimen Collection Kit is also acceptable for specimen collection.
Limitations
A negative result does not preclude the possibility of an existing infection. Test results can be influenced by factors such as improper specimen collection, target levels below the assay's limit of detection, and inadequate specimen handling. Therefore, interpretation of the results should consider other clinical and lab data. The resistance test developed by Labcorp has not been cleared or approved by the FDA, as such clearance or approval is not deemed necessary by the FDA.
Methodology
PCR-based (NAA)
Biomarkers
LOINC Codes
- 100706-1
- 100706-1
Result Turnaround Time
3-4 days
Related Documents
For more information, please review the documents below
Specimen
Cervical Swab
Volume
One Aptima® swab (endocervical, vaginal or male urethral)
Minimum Volume
One Aptima® swab (endocervical, vaginal or male urethral)
Container
Aptima® Multitest Swab Specimen Collection Kit or Aptima® Unisex Swab Specimen Collection Kit
Collection Instructions
Endocervical swab: Remove excess mucus from the cervical os using the cleaning swab, insert the specimen collection swab into the canal, rotate for adequate sampling, and place it into the transport tube.
Storage Instructions
Maintain specimen at room temperature or refrigerate (2°C to 30°C).
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 30 days |
| Refrigerated | 30 days |