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HPV 16 & 18/45 Genotype

Specimen:

Collect

  • Gynecological Sample in Aptima Kit-Transfer Kit (Green)

Also Acceptable:
  • Gynecological Sample in ThinPrep PreservCyt Media

Submit

  • Gynecological Sample in Aptima Kit-Transfer Kit (Green). Submit Ambient.

Also Acceptable:
  • Gynecological Sample in ThinPrep PreservCyt Media. Submit Ambient.

Special Handling

  • Collect the sample as usual according to the manufacturer's instructions.
    Add on testing for PAP vials: Surepath - valid for 10 days from Collection. Thin Prep - valid for 30 days from Collection

Rejection Criteria

  • Cervical swabs in Digene HC Cervical Sampler; Cytyc media w/o cervical brush/broom; Swabs; Digene vials are not acceptable; Unprocessed SurePath vials are not acceptable; Vaginal Swabs

Stability

Ambient: 1 Month(s); Refrigerated: 1 Month(s); Frozen: Unacceptable; Incubated: Unacceptable

Methodology

  • Invader(R) signal amplification

Performed

Monday, Wednesday

Reported

3-6 Day(s)

CPT Codes

  • 87625

Interpretive Data

Please see report for interpretive data.

The Aptima HPV 16 18/45 is an in vitro nuclei acid amplification test for the qualitative detection of E6/E7 viral messenger RNA (mRNA) of the human papillomavirus (HPV) types 16, 18, and 45 in cervical specimens from women with Aptima HPV Assay positive results. The Assay can differentiate HPV 16 from HPV 18 and/or 45, but does not differentiate between HPV 18 and HPV 45. The analytical performance characteristics of this assay, when used to test Surepath specimens, have been determined by Medical Lab Associates.

Components

  • 93693 - HPV 16 GENOTYPE
  • 93694 - HPV18/45 GENOTYPE
Last Updated: December 10, 2024 @ 10:13 am

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