Candida Six-species Profile, NAA

CPT: 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

Detect the presence of Candida albicans, Candida glabrata, Candida tropicalis, Candida parapsilosis, Candida lusitaniae, and Candida krusei DNA in vaginal samples as an aid to the diagnosis of vulvovaginal candidiasis in symptomatic women


Limitations

Candida parapsilosis cannot be differentiated from Candida metapsilosis or Candida orthopsilosis using this assay.

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
180010 Candida 6 Species Profile, NAA 180056 Candida albicans, NAA 69562-7
180010 Candida 6 Species Profile, NAA 180057 Candida glabrata, NAA 69563-5
180010 Candida 6 Species Profile, NAA 180053 C parapsilosis/tropicalis 62460-1
180010 Candida 6 Species Profile, NAA 180015 Candida lusitaniae, NAA 72390-8
180010 Candida 6 Species Profile, NAA 180016 Candida krusei, NAA 72389-0

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