Test Code Billings Clinic: 9008 Trichomonas RNA Amp
Performing Laboratory
Billings Clinic Laboratory: Molecular Microbiology
Useful For
- The AptimaTM Trichomonas vaginalis assay is an in vitro qualitative nucleic acid amplification test for the detection of ribosomal RNA from Trichomonas vaginalis and is used as an aid in the diagnosis of trichomoniasis using the PantherTM System.
- This assay may be used to test the specimens from symptomatic or asymptomatic patients.
Methodology
Target Capture, Transcription Mediated Amplification (TMA) and Hybridization Protection Assay (HPA)
Specimen Requirements
The following swab specimens must be collected using an APTIMA Collection Unisex Swab. These swabs are contained in the APTIMA Collection Kit.
Specimen Type: Endocervix
Container/Tube: APTIMA Collection Unisex Swab
Specimen Volume: Swab
Collection Instructions:
- Use cleaning swab (white shaft) to remove excess mucus from endocervix and discard.
- Insert second swab (blue shaft) 1 to 1.5 cm into endocervical canal, and rotate swab gently for 30 seconds. Avoid touching vaginal wall when removing swab.
- Place second swab into transport tube provided in collection kit. Snap off swab at score line so swab fits into closed tube.
- Cap tube securely, and label tube with patient's entire name, and date and time of collection.
- Transport and store swab container at 2 to 30° C (refrigerate is preferred temperature).
- Swab is stable at 2 to 30° C for 60 days. If longer storage is needed, freeze at -20 to -70 degrees C for 12 months.
Specimen Type: Vaginal (Self-collection)
Please see "Vaginal Self-Collection Guide" under "Resources"
Storage/Stability
Aptima Collection Swab - 5 days room temperature
Reject Due To
- Specimens collected using a swab that is not an Aptima Collection Kit swab
- Specimens collected from male patients
Reference Values
Negative
Interpretation:
- Negative Negative for Trichomonas vaginalis
- Positive Positive for Trichomonas vaginalis
- Invalid This specimen may be grossly contaminated with mucous or another interfering substance which prevented adequate amplification. Please resubmit.
- Equivocal Indeterminate - a second specimen should be submitted to determine infection status
Day(s) Test Set Up
Monday through Friday
Test Classification and CPT Coding
87661 - Infectious agent detection by nucleic acid (DNA or RNA); Trichomonas vaginalis, amplified probe technique
LOINC Code Information
Reporting Name | LOINC Code |
T. vaginalis, RNA | 46154-1 |