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HelpTest Code CVRNA Candida Vaginitis, Nucleic Acid Amplification RNA, Vaginal
Necessary Information
Specimen Required
Specimen Type: Vaginal
Supplies: Aptima Multitest Swab Collection Kit (T584)
Container/Tube: Aptima Multitest Swab
Specimen Volume: Swab
Collection Instructions:
1. Specimens must be collected using the Aptima Multitest Swab Collection Kit.
2. Insert swab (pink shaft) about 5 cm past introitus and rotate gently for 30 seconds.
3. Place swab into transport tube provided in collection kit. Snap off swab at score line so swab fits into closed tube.
4. Cap tube securely, and label tube with patient's entire name and collection date and time.
5. Maintain swab container at 2 to 30° C (refrigerate temperature is preferred) and transport within 30 days of collection. If longer storage is needed, freeze at -20 to -70° C up to 60 days.
Useful For
Aiding in the diagnosis of Candida vaginitis
This test is not intended for use in medico-legal applications.
Method Name
Transcription Mediated Amplification
Reporting Name
Candida vaginitis, Amplified RNASpecimen Type
VaginalSpecimen Minimum Volume
See Specimen Required
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Vaginal | Refrigerated (preferred) | 30 days | APTIMA VIAL |
| Frozen | 60 days | APTIMA VIAL | |
| Ambient | 30 days | APTIMA VIAL |
Reject Due To
| Incorrect swab Transport tubes containing more than one swab |
Reject |
Clinical Information
This test is intended to aid in the diagnosis of vulvovaginal candidiasis from vaginal samples collected from symptomatic individuals. Vaginitis is characterized by a spectrum of signs and symptoms, including vaginal/vulvar irritation, odor, discharge, and pruritus. Vaginitis may develop as a result of mechanical and/or chemical irritants (eg, feminine hygiene products, contraceptive materials), or due to a dysbiosis of the microbiota in the vaginal tract. Up to 90% of vaginitis cases are infectious due to Bacterial vaginosis (BV), vulvovaginal candidiasis (Candida vaginitis, CV) and/or trichomoniasis (Trichomonas vaginalis, TV). BV, CV and TV individually account for 22% to 50%, 17% to 39%, and 4% to 35% of vaginitis cases, respectively.
CV, commonly known as a yeast infection, is the second most frequent cause of vaginitis. CV is characterized by an overgrowth of Candida species in the vaginal tract and is associated with development of inflammation, abnormal vaginal discharge, vaginal soreness, pruritus, dyspareunia, and external dysuria. Up to 89% of CV cases are caused by C albicans, while non-albicans species may be responsible for 11%. C glabrata, which is responsible for the majority of non-albicans CV in the U.S., has decreased susceptibility to standard antifungal regiments for CV as compared to C albicans, which is why C glabrata is specifically reported by this assay.
Reference Values
Candida glabrata
Negative
Candida species group (C albicans, C tropicalis, C parapsilosis, C dubliniensis)
Negative
Interpretation
Candida species group (C albicans, C tropicalis, C parapsilosis, C dubliniensis):
Positive: Candida albicans, C tropicalis, C parapsilosis and/or C dubliniensis RNA detected. Individual organisms are not identified or reported by this assay. Results should be interpreted alongside clinical presentation. Up to 21% of asymptomatic patients may be positive by this assay.
Negative: No RNA detected from Candida albicans, C tropicalis, C parapsilosis or C dubliniensis. A negative result does not exclude infection.
Inconclusive: Repeat testing on a new sample is recommended if clinically indicated.
Candida glabrata:
Positive: Candida glabrata RNA detected. Results should be interpreted alongside clinical presentation. Up to 9% of asymptomatic patients may be positive for C glabrata this assay.
Negative: No RNA detected from Candida glabrata. A negative result does not exclude infection.
Inconclusive: Repeat testing on a new sample is recommended if clinically indicated.
Cautions
The effects of tampon use, douching, and specimen collection variables have not been evaluated for their impact on assay performance.
This report is intended for clinical monitoring or management of patients; it is not intended for use in medico-legal applications.
Appropriate specimen collection and handling is necessary for optimal assay performance.
Therapeutic failure or success cannot be determined with this assay since nucleic acid may persist following appropriate antimicrobial therapy.
A negative result does not preclude a possible infection because results are dependent on adequate specimen collection. Test results may be affected by improper specimen collection, technical error, specimen mix-up, or low numbers of organisms in the specimen (target levels below the assay limit of detection).
Therapeutic failure or success cannot be determined since nucleic acid may persist following appropriate antimicrobial therapy.
Performance of the assay has not been evaluated in women younger than 14 years.
Collection and testing of patient-collected vaginal swab specimens with the assay is not intended to replace clinical examination. Vaginal infections may result from other causes or concurrent infections may occur.
Interference with the assay was observed in the presence of the following substances: Tioconazole 6.5% Ointment (3% W/V, all analytes), Vaginal Moisturizing Gel (1% W/V, C spp; 5% W/V, C glabrata; 3% W/V, TV), and Glacial Acetic Acid (5% V/V, C spp only).
The following organism was observed to cross-react above the stated concentrations:
Candida famata at concentrations higher than 5x105 CFU/mL.
Competitive interference was observed in co-infected samples for the combination of low
C glabrata (3X LoD) and high T vaginalis (1x105 or 1x104 cells/mL).
Method Description
The Aptima CV/TV kit is used for this testing, however only the CV result is reported. This assay is an in vitro nucleic acid amplification test for the detection of RNA from microorganisms associated with vulvovaginal candidiasis and trichomoniasis. The assay utilizes real time transcription-mediated amplification (TMA) to detect and qualitatively report results for the following organisms: Candida species group (C albicans, C tropicalis, parapsilosis, C dubliniensis), Candida glabrata, and Trichomonas vaginalis (TV). The Panther system detects and discriminates between four fluorescent signals corresponding to Candida species group, C glabrata, TV, and IC amplification products. The Panther system software uses an Aptima CV/TV assay-specific algorithm that interprets the amplification signal emergence times to generate a Positive or Negative status for each target organism in the sample. Note, the TV component of this kit is not reported. (Package insert: Aptima CV/TV Assay, AW-23713-001. Hologic, Inc; Rev 001, 03/2023)
Day(s) Performed
Monday through Sunday
Report Available
1 to 4 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Test Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
87481
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| CVRNA | Candida vaginitis, Amplified RNA | 92703-8 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 621517 | Candida species, Amplified RNA | 94422-3 |
| 621518 | Candida glabrata, Amplified RNA | 94421-5 |