Test Code HPV PCR HPV PCR W 16/18 GENOTYPE
Methodology
The Cervista HPV HR test uses the Invader chemistry, a signal amplification method for detection of specific nucleic acid sequences. Cervista HPV HR Detects the DNA from 14 high-risk HPV types (16,18,31,33,35,39,45,51,52,56,58,59,66,and 68) in cervical specimens, however, it cannot determine the specific HPV type present.
The Cervista HPV HR test is indicated:
- 1. To screen patients with atypical squamous cells of undetermined significance (ASC-US) cervical cytology results to determine the need for referral to colposcopy.
- 2. In women 30 years and older, the Cervista HPV HR test can be used with cervical cytology to adjunctively screen to assess the presence or absence of high-risk HVP types. This information, together with the physician’s assessment of cytology history, other factors, and professional guidelines, may be used to guide patient management.
Specimen Requirements
Cervical specimen collected in ThinPrep® Solution.
Note:
Cervical specimens can be stored at room temperature (20-30° C) in ThinPrep® solution for up to 8 weeks prior to performing the test.
Day(s) Test Set Up
Monday through Friday
Batched Daily
Maximum Laboratory Time
72 to 96 hours
Specimen Stability
Ambient
Refrigerated NO
Frozen NO
Reference Values
Negative
Note: An interpretive report will be provided.
Performing Laboratory
Logan Health Medical Center Laboratory
Test Classification and CPT Coding
87624