Genital Mycoplasma Profile, NAA, Urine
Use
Detect Mycoplasma genitalium, Mycoplasma hominis, Ureaplasma spp
Special Instructions
Not provided.
Limitations
The test has been developed and its performance characteristics determined by LabCorp. It has not been cleared or approved by the FDA, as such clearance or approval is not considered necessary by the FDA. Additionally, improper collection, storage, or handling of specimens could affect test sensitivity.
Methodology
PCR-based (NAA)
Biomarkers
Mycoplasma genitalium
MicroorganismMycoplasma hominis
MicroorganismUreaplasma spp
Microorganism
LOINC Codes
- 68546-1 - M hominis DNA Spec Ql NAA+probe
- 68547-9 - Ureaplasma DNA Spec Ql NAA+probe
- 88226-6 - M genitalium DNA Ur Ql NAA+probe
Result Turnaround Time
3-4 days
Related Documents
For more information, please review the documents below
Specimen
Urine
Volume
2 mL of a 20 to 30 mL urine collection
Minimum Volume
Not provided
Container
Aptima® urine transport
Collection Instructions
Patient should not urinate for at least one hour prior to collection. Collect first-catch urine (approximately 20-30 mL) into a urine collection cup, add to the Aptima® Combo 2 urine collection device, ensuring final volume is between the two black lines.
Patient Preparation
Do not urinate for at least one hour prior to specimen collection.
Storage Instructions
Maintain at room temperature or refrigerate (2°C to 30°C).
Causes for Rejection
Specimens with incorrect patient identification, unlabeled, inappropriate transport conditions, received after prolonged delay (usually >72 hours), leaked in transit, incorrect transport device, or inappropriate volume in transport.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 30 days |
| Refrigerated | 30 days |
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