2001
DOI: 10.1046/j.1526-0976.2001.51006.x
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Human Papillomavirus Testing for Triage in a Referral Population

Abstract: Although HPV high-risk positive results correlate with high-grade histology, it is associated with significant false negatives. The HPV low-risk test is not clinically useful. These tests were poor methods to triage patients in our population.

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Cited by 2 publications
(2 citation statements)
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“…According to the manufacturer, Qiagen, “The digene HC2 HPV DNA Test is an in vitro nucleic acid hybridization assay with signal amplification using microplate chemiluminescence for the qualitative detection of 18 types of HPV DNA in cervical specimens. The digene HC2 HPV DNA Test can differentiate between two HPV DNA groups, low‐ and high‐risk types [68].” The HPV tests on the market only help doctors screen patients for the presence of a group of HPVs that may cause cellular changes, which may lead to cervical cancer in some patients if not treated. These commercial test kits are designed to screen 13 “high‐risk” HPV genotypes out of about 40 genotypes commonly found in the anogenital regions of women and men.…”
Section: Introductionmentioning
confidence: 99%
“…According to the manufacturer, Qiagen, “The digene HC2 HPV DNA Test is an in vitro nucleic acid hybridization assay with signal amplification using microplate chemiluminescence for the qualitative detection of 18 types of HPV DNA in cervical specimens. The digene HC2 HPV DNA Test can differentiate between two HPV DNA groups, low‐ and high‐risk types [68].” The HPV tests on the market only help doctors screen patients for the presence of a group of HPVs that may cause cellular changes, which may lead to cervical cancer in some patients if not treated. These commercial test kits are designed to screen 13 “high‐risk” HPV genotypes out of about 40 genotypes commonly found in the anogenital regions of women and men.…”
Section: Introductionmentioning
confidence: 99%
“…Digene Hybrid Capture 2 (HC2) test, the only test approved by the U.S. Food and Drug Administration (FDA), is commonly used to determine if a cervicovaginal cell suspension contains "high-risk" oncogenic HPVs [2], often functioning as a triage for colposcopic evaluation of the cytologically borderline cases [3-5]. However, it is now recognized that persistent infection of a "high-risk" HPV, not the mere presence of the HPV virus itself, is the pivotal promoter in causing cervical precancerous lesions and cancer [6-9].…”
Section: Introductionmentioning
confidence: 99%