VAGINOSIS/VAGINITIS PANEL BASIC

Test Code
LAB2248


Quest Code
10119


Alias/See Also
Vaginitis


CPT Codes
81513, 87481 (x2), 87661<br><strong>CPT coding may differ dependent on payer rules which may impact prior authorization testing.</strong><br><strong>Please direct any questions regarding CPT coding to the payer being billed.</strong>

Includes
SureSwab® Advanced Bacterial Vaginosis (BV), TMA
SureSwab® Advanced Candida Vaginitis (CV), TMA
Trichomonas vaginalis (TV), TMA


Preferred Specimen
1 vaginal swab collected in Aptima® Multitest Transport Tube


Minimum Volume
1 swab


Instructions
Follow instructions in the Aptima Multitest Collection Kit (orange label).
Age restrictions may apply. See individual tests for further information.


Transport Container
Aptima® Multitest Transport Tube


Transport Temperature
Room temperature


Specimen Stability
Room temperature: 30 days
Refrigerated: 30 days
Frozen: 60 days


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Transport tube with no swab • Transport tube with 2 swabs • Transport tube containing cleaning swab • Transport tube with non-Aptima swabs • Transport tube submitted with swab inverted • Swab submitted in viral transport media • Samples with excess mucus • Specimens submitted in Aptima tubes with pierced foil lids • Patients less than 14 years of age


Methodology
Transcription Mediated Amplification (TMA)

Reference Range
SureSwab® Adv Bacterial Vaginosis (BV), TMANegative
   
SureSwab® Adv Candida Vaginitis (CV), TMA 
  Candida speciesNot detected
  Candida glabrataNot detected
   
Trichomonas vaginalis (TV), TMANot detected


Clinical Significance
The assay is intended to aid in the diagnosis of vaginitis using clinician-collected and patient-collected vaginal swab specimens from individuals with a clinical presentation consistent with vaginitis. Testing for bacterial vaginosis (BV), vulvovaginal candidiasis and trichomoniasis are included.
The BV test is an in vitro nucleic acid amplification test that utilizes real time transcription-mediated amplification (TMA) for detection and quantitation of ribosomal RNA from bacteria associated with bacterial vaginosis (BV), including Lactobacillus (L. gasseri, L. crispatus, and L. jensenii), Gardnerella vaginalis, and Atopobium vaginae. The assay reports a qualitative result for BV and does not report results for individual organisms.
For vulvovaginal candidiasis and trichomoniasis, a real time transcription-mediated amplification (TMA) assay is used to detect and qualitatively report results for Candida species group (C. albicans, C. tropicalis, C. parapsilosis, C. dubliniensis), C. glabrata, and Trichomonas vaginalis.


Performing Laboratory
Quest Diagnostics-Lenexa
10101 Renner Blvd
Lenexa, KS 66219-9752



Last Updated: February 21, 2022


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.