- Tech Only CPT 87481 X2, 87511, 87661, 87798, 87491, 87591
- Tech Pro CPT
- PowerPath Code VP Aptima
- Schedule Monday - Friday
- Turn Around Time 24 to 48 hours
- Disease State Urogenital Infection, Vaginitis
- Methodology Transcription-Mediated Amplification
Unisex swab in Aptima tube
The LDT test is intended for use in the detection and identification of Candida species, Candida galbrata, Gardnerella vaginali, Lactobacillus, Trichomonas vaginalis and Chlamydia trachomatis, Neisseria gonorrhea nucleic acid in vaginal fluid specimens from patients with symptoms of vaginitis/vaginosis.
Storage and Transportation
Room temperature - Store in CellSwab (Aptima) transport tube. Stable 2-30°C / 60 days.
Cause for Rejection
- less than 2.0 mls
- No swab in Aptima tube
FDA approved for the detection of Chlamydia trachomatis and Neisseria gonorrhea, two of the most common sexually transmitted infections worldwide.
FDA approved for the detection of Trichomonas vaginalis LDT for Candida species, Candida Glabrata, Gardnerella vaginalis lactobacillus.