Vaginitis Panel (Aptima) – CellSwab + CT/GC
CellSwab, Bacterial Vaginitis (BV/CV) swab, TV
- Tech Only CPT 87481x2, 87661,87491,87591,81513, 87591, 87492
- Tech Pro CPT
- PowerPath Code VP Aptima 2 (BVa-CB*, BVa-GV*, BVa-TV*, BVa-CS*, BVa-LA*, zGC, zCT)
- Schedule Monday - Friday
- Turn Around Time Within 3 days of receipt
- Disease State Trichomonas Vaginalis, Urogenital Infection, Vaginitis
- Methodology Transcription-Mediated Nucleic Acid Amplification
Organs
Specimen Requirements
Clinician or patient collected vaginal swab submitted in Hologic Aptima Multitest Direct Load Tube (Aptima Orange Tube)
Clinical Significance
Vaginitis syndrome is characterized by a spectrum of conditions: vaginal and vulvar irritation, odor, discharge, and pruritus. Up to 90% of infectious vaginitis cases are caused by BV, vulvovaginal candidiasis (candida vaginitis) and trichomoniasis (trichomonas vaginalis vaginitis).
Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (GC) infections are two of the most common sexually transmitted infections worldwide.
Tests for Gardnerella vaginalis, Candida species, Candida glabrata, Trichomonas vaginalis, Chlamydia trachomatis, and Neisseria gonorrhoeae
Required Patient Info
2 patient identifiers
Storage and Transportation
15°C - 30°C
Cause for Rejection
Improper collection medium (i.e., not in a Hologic collection tube), specimen lacking swab, improper or inadequate patient identification
Retention
4 weeks from testing