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HelpTest Code MHPRP Metamycoplasma hominis, Molecular Detection, PCR, Plasma
Reporting Name
Mycoplasma hominis PCR, PPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Useful For
Rapid, sensitive, and specific identification of Metamycoplasma hominis from plasma
This test is not intended for medicolegal use.
Method Name
Real-Time Polymerase Chain Reaction (PCR) using LightCycler and Fluorescent Resonance Energy Transfer (FRET)
Ordering Guidance
Shipping Instructions
Ship specimen refrigerated.
Specimen Required
The high sensitivity of amplification by polymerase chain reaction requires the specimen to be processed in an environment in which contamination of the specimen by Metamycoplasma hominis DNA is unlikely.
Collection Container/Tube:
Preferred: Lavender top (EDTA)
Acceptable: Royal blue top (EDTA), pink top (EDTA)
Submission Container/Tube: Screw-capped, sterile container
Specimen Volume: 1 mL
Collection Instructions: Centrifuge and aliquot plasma into a sterile vial within 24 hours of collection.
Specimen Type
Plasma EDTASpecimen Minimum Volume
0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Plasma EDTA | Refrigerated (preferred) | 7 days | |
| Frozen | 7 days |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitabilityReference Values
Not applicable
Interpretation
A positive polymerase chain reaction (PCR) result for the presence of a specific sequence found within the Metamycoplasma hominis tuf gene indicates the presence of M hominis DNA in the specimen.
A negative PCR result indicates the absence of detectable M hominis DNA in the specimen, but it does not rule-out infection as false-negative results may occur due to inhibition of PCR, sequence variability underlying the primers and probes, or the presence of M hominis in quantities less than the limit of detection of the assay.
Day(s) Performed
Monday through Friday
Report Available
3 to 4 daysTest Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
87798
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| MHPRP | Mycoplasma hominis PCR, P | 68546-1 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| MPSRC | Specimen Source | 31208-2 |
| 44134 | Mycoplasma hominis PCR, P | 68546-1 |