Urogenital Ureaplasma and Mycoplasma Species by PCR
Also known as: UR MYCOPCR
Use
This test is used to detect and speciate Ureaplasma parvum, U. urealyticum, Mycoplasma hominis, and M. genitalium. It may be considered for cases of nongonococcal urethritis. These pathogens are relevant in the clinical diagnosis of urogenital infections, especially in patients presenting with symptoms of nongonococcal urethritis. Identifying the specific species of Ureaplasma and Mycoplasma is critical for appropriate clinical management and treatment decisions.
Special Instructions
Specimen source is required. Ensure the specimen is sent to the laboratory frozen to maintain stability and ensure accurate test results. This test is developed and its performance characteristics determined by ARUP Laboratories, and it is intended for clinical use in a CLIA-certified laboratory.
Limitations
A negative result does not rule out the presence of PCR inhibitors in the patient specimen or the presence of test-specific nucleic acid in concentrations below the level of detection by this test. This test is not cleared or approved by the FDA but is performed in a CLIA-certified laboratory, which may limit its use in certain clinical scenarios depending on regulatory requirements.
New York Approved
Methodology
PCR-based (PCR)
Biomarkers
LOINC Codes
- 31208-2
- 69933-0
- 51988-4
- 68546-1
- 69935-5
Result Turnaround Time
2-5 days
Related Documents
For more information, please review the documents below
Specimen
Other
Volume
Not provided
Minimum Volume
Not provided
Container
viral transport media (ARUP supply #12884)
Collection Instructions
Transfer genital swab to viral transport media available online through eSupply using ARUP Connect or contact ARUP Client Services.
Storage Instructions
Frozen
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 48 hours |
| Refrigerated | 10 days |
| Frozen | 14 days |
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