Vaginitis Plus (VG+), NuSwab®

CPT: 87491; 87591; 87661; 87798(x3); 87801
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Expected Turnaround Time

3 - 4 days



Related Documents

For more information, please view the literature below.

Optimal Specimen Collection Device Flyer (Women's Health)


Specimen Requirements


Specimen

Vaginal swab


Volume

One swab


Minimum Volume

One swab


Container

Aptima® Multitest Swab Specimen Collection Kit or Aptima® Unisex Swab Specimen Collection Kit


Collection

Vaginal swab: Collect vaginal fluid sample using the Aptima® swab by contacting the swab to the lower third of the vaginal wall and rotating the swab for 10 to 30 seconds to absorb fluid. Immediately place the swab into the transport tube and carefully break the swab shaft against the side of the tube. Tightly screw on the cap.


Storage Instructions

Maintain specimen at room temperature or refrigerate (2°C to 30°C).


Stability Requirements

Temperature

Period

Room temperature

30 days

Refrigerated

30 days

Frozen

Not acceptable


Causes for Rejection

Specimen with incorrect patient identification; unlabeled specimen; inappropriate specimen transport conditions, including specimens received frozen; specimens received after prolonged delay (usually >72 hours); specimen leaked in transit; specimen in expired transport or incorrect transport device; specimens with inappropriate source for test requested; specimen with fixative or additives; Aptima® urine transport; Aptima® swab transport >30 days from collection; Aptima® swab specimen without a swab; cleaning swab (white-shaft swab) in Aptima® swab transport; any non-Aptima® swab submitted in Aptima® transport device; transport device with multiple swabs; bloody or grossly mucoid specimens; bacterial swabs; specimen in ProbeTec™ UPT transport; ProbeTec™ Q-swabs


Test Details


Use

This test is intended to be used as an aid to the diagnosis of bacterial vaginosis (BV) in women with a clinical presentation consistent with this disorder. The BV test utilizes semiquantitative PCR analysis of the three most predictive marker organisms (Atopobium vaginae, BVAB-2, and Megasphaera-1) to generate a total score that correlates directly with the presence or absence of BV. In this test system, samples with a total score of 0 to 1 are considered negative for BV, samples with a score of 3 to 6 are positive for BV, and samples with a score of 2 are indeterminate for BV. Used to detect the presence of Candida albicans and Candida glabrata DNA in vaginal samples as an aid to the diagnosis of vulvovaginal candidiasis in symptomatic women. Also used in the diagnosis of Chlamydia trachomatis, Neisseria gonorrhoeae, and Trichomonas vaginalis infections.


Limitations

This test was developed and its performance characteristics determined by Labcorp. It has not been cleared or approved by the Food and Drug Administration. The FDA has determined that such clearance or approval is not necessary.


Methodology

Nucleic acid amplification (NAA)


LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
180021 NuSwab Vaginitis Plus (VG+) 92703-8 180061 Atopobium vaginae Score 69565-0
180021 NuSwab Vaginitis Plus (VG+) 92703-8 180062 BVAB 2 Score 69566-8
180021 NuSwab Vaginitis Plus (VG+) 92703-8 180063 Megasphaera 1 Score 69567-6
180021 NuSwab Vaginitis Plus (VG+) 92703-8 180056 Candida albicans, NAA 69562-7
180021 NuSwab Vaginitis Plus (VG+) 92703-8 180057 Candida glabrata, NAA 69563-5
180021 NuSwab Vaginitis Plus (VG+) 92703-8 180087 Trich vag by NAA 62461-9
180021 NuSwab Vaginitis Plus (VG+) 92703-8 180097 Chlamydia trachomatis, NAA 21613-5
180021 NuSwab Vaginitis Plus (VG+) 92703-8 180104 Neisseria gonorrhoeae, NAA 32705-6

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