SureSwab®, Mycoplasma/Ureaplasma Panel, Real-Time PCR [91477]

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Test Code
MUPANL


Alias/See Also
91477


CPT Codes
87563, 87798 (x3)

Includes
SureSwab®, Mycoplasma hominis, Real-Time PCR
Mycoplasma genitalium, rRNA, TMA
SureSwab®, Ureaplasma species, Real-Time PCR


Preferred Specimen
1 vaginal swab collected in an Aptima® Vaginal Swab Collection Kit or Multitest Collection Kit (orange label), or
1 male urethral swab collected in an Aptima® Unisex Swab Specimen Collection Kit (white label), or
2 mL male urine collected in an Aptima® Urine Transport Tube


Minimum Volume
1 swab • 2 mL urine


Other Acceptable Specimens
No other acceptable specimens


Instructions
Vaginal Swabs: Follow instructions in the Aptima® Vaginal Swab Collection Kit or Multitest Collection Kit (orange label).

Male Urethral Swabs: Follow instructions in the Aptima® Unisex Swab Specimen Collection Kit (white label).

Swab specimen collection kit (orange or white label). Excess mucus should be removed prior to sampling.

Male Urine: Direct patient to provide a first-catch urine (a maximum of 20-30 mL of the initial urine stream) into a urine collection cup free of any preservatives. 2 mL of urine specimen must be transferred into the Aptima® urine specimen transport within 24 hours of collection and before being assayed. Use the tube provided in the urine specimen collection kit. The fluid (urine plus transport media) level in the urine transport tube must fall within the clear pane on the tube label.


Transport Temperature
Room temperature


Specimen Stability
Room temperature: 14 days
Refrigerated: 14 days
Frozen: 30 days


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Transport tubes with 2 swabs • Transport tubes with Non-APTIMA® swabs • Swab transport tubes with no swab • Swab submitted in non-APTIMA® transport containers • Urine samples where the fluid level is not between the black fill


Methodology
See individual tests

FDA Status
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Setup Schedule
Set up: Mon-Sat; Report available: 4 days


Reference Range
Mycoplasma hominis, Real-Time PCR Not detected
Mycoplasma genitalium, rRNA, TMA Not detected
Ureaplasma species, Real-Time PCR  
  U. parvum DNA Not detected
  U. urealyticum DNA Not detected


Clinical Significance
Mycoplasma and Ureaplasma spp. have been associated with genital tract infection. M. genitalium has been implicated in cervicitis, endometritis, and PID. M. hominis has also been associated with cervicitis and is present in increased numbers in vaginosis. Ureaplasma spp. have been linked to upper genitourinary tract infection and to premature labor and abortion. Because of their nature, these organisms are not routinely cultured and are better detected by molecular methods.
Recently, by molecular means two groups of Ureaplasma spp. have been distinguished- U. parvum and U. urealyticum, with the former being more prevalent in the lower genital tract of a healthy woman. It is not clear which species more predominantly causes infection. M. hominis and the ureaplasmas appear to be opportunists when they infect the upper genitourinary tract. These organisms have also been targeted as having a possible role in infertility, although this remains a gray area.


Performing Laboratory
Quest Diagnostics Nichols Institute
14225 Newbrook Drive
Chantilly, VA 20153


Last Updated: November 30, 2021


The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.