#ExistRefRangeSet>
Reference Interval:
#ExistRefRange>Negative
*ExistRefRange>
#ExistRefRangeTable> | Test Number
| Components
| Reference Interval
| | | Human Papillomavirus (HPV) DNA Probe, High Risk Only
| Negative
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*ExistRefRangeTable>
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*ExistRefRangeSet>
#ExistInterpDataSet>
| Interpretive Data: |
#ExistInterpData>This test detects the high-risk HPV genotypes 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59 and 68 associated with cervical cancer and its precursor lesions. However, cross-reactions with other genotypes may occur. Results should be correlated with cytologic and histologic findings. Sensitivity may be affected by cellularity of specimen.
This test is intended for medical purposes only and is not valid for the evaluation of suspected sexual abuse or for other forensic purposes.
HPV testing should not be used for screening or management of atypical squamous cells of undetermined significance (ASCUS) in women under age 21.
*ExistInterpData>
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*ExistInterpDataSet>
#ExistNote>
| Note: |
A negative result does not rule out the presence of an HPV genotype absent from the test panel, a low level infection, or specimen sampling error.
|
*ExistNote>
#ExistCPT>
| CPT Code(s): |
87621
|
*ExistCPT>
#ExistCrossReferences>
Cross References: |
Condyloma (Human Papillomavirus (HPV) DNA Probe, High Risk, Cervical Brush (Digene)), Genital Warts (Human Papillomavirus (HPV) DNA Probe, High Risk, Cervical Brush (Digene)), HPV High-Risk (Human Papillomavirus (HPV) DNA Probe, High Risk, Cervical Brush (Digene)), Hybrid Capture (Human Papillomavirus (HPV) DNA Probe, High Risk, Cervical Brush (Digene)) |
*ExistCrossReferences>
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