3 - 4 days
Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.
For more information, please view the literature below.
Aptima® vaginal or unisex swab
Vaginal swab: Collect vaginal fluid sample using the Gen-Probe® 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.
Maintain specimen at room temperature or refrigerate (2°C to 30°C).
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−Gen-Probe® 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
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.
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.
Nucleic acid amplification (NAA)
|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||45084-1|
|180021||NuSwab Vaginitis Plus (VG+)||92703-8||180104||Neisseria gonorrhoeae, NAA||32705-6|
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