|
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z # |
SureSwab® Advanced Bacterial Vaginosis (BV), CT/NG, TMA
Test Code10123
CPT Codes
87491, 87591, 81513
Includes
SureSwab® Advanced Bacterial Vaginosis (BV), TMA
Chlamydia/Neisseria gonorrhoeae RNA, TMA, Urogenital
Chlamydia/Neisseria gonorrhoeae RNA, TMA, Urogenital
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)
Transport Container
Aptima® Multitest Transport Tube
Transport Temperature
Room temperature
Specimen Stability
Room temperature: 30 days
Refrigerated: 30 days
Frozen: 60 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
Methodology
Transcription Mediated Amplification (TMA)
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 U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Setup Schedule
Set up: Daily; Report available: Next day
Reference Range
SureSwab® Adv Bacterial Vaginosis (BV), TMA | Negative |
C. trachomatis RNA, TMA, Urogenital | Not detected |
N. gonorrhoeae RNA, TMA, Urogenital | Not detected |
Clinical Significance
The assay is intended to aid in the diagnosis of Bacterial vaginosis (BV), and Chlamydia trachomatis/ Neisseria gonorrhoeae using clinician-collected and patient-collected vaginal swab specimens from individuals with a clinical presentation consistent with vaginitis and/or vaginosis.
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 Chlamydia trachomatis and Neisseria gonorrhoeae, a target capture assay is utilized for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis and/or Neisseria gonorrhoeae.
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 Chlamydia trachomatis and Neisseria gonorrhoeae, a target capture assay is utilized for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis and/or Neisseria gonorrhoeae.