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Laboratory Test Detail

Last Updated: April 24, 2024 @ 9:13 am

93697

HPV 16 & 18/45 Genotype

Specimen:Collect:
  • Gynecological Sample in One Liquid Pap Media
Submit:
  • 4 mL (Min:2 mL) Gynecological Sample in Liquid Pap 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
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