Type-specific HPV and Pap test results among low-income, underserved women: providing insights into management strategies
Supporting Files
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May 06 2014
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File Language:
English
Details
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Alternative Title:Am J Obstet Gynecol
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Personal Author:
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Description:OBJECTIVE
The primary cervical cancer screening strategy for women over age 30 is high-risk human papillomavirus (HPV) testing combined with Papanicolaou (Pap) testing (cotesting) every 5 years. This combination strategy is a preventive service that is required by the Affordable Care Act to be covered with no cost-sharing by most health insurance plans. The cotesting recommendation was made based entirely on prospective data from an insured population that may have a lower proportion of women with HPV positive and Pap negative results (ie, discordant results). The discordant group represents a very difficult group to manage. If the frequency of discordant results among underserved women is higher, health care providers may perceive the cotesting strategy to be a less favorable screening strategy than traditional Pap testing every 3 years.
STUDY DESIGN
The Centers for Disease Control and Prevention’s Cervical Cancer Study was conducted at 15 clinics in 6 federally qualified health centers across Illinois. Providers at these clinics were given the option of cotesting for routine cervical cancer screening. Type-specific HPV detection was performed on residual extracts using linear array.
RESULTS
Pap test results were abnormal in 6.0% and HPV was positive in 7.2% of the underserved women screened in this study (mean age, 45.1 years). HPV prevalence decreased with age, from 10.3% among 30- to 39-year-olds to 4.5% among 50- to 60-year-olds. About 5% of the women had a combination of a positive HPV test and normal Pap test results; HPV 16/18 was identified in 14% of discordant women.
CONCLUSION
The rate of discordant results among underserved women was similar to those reported throughout the US in a variety of populations. Typing for HPV 16/18 appears to assist in the management in a small proportion of women with discordant results.
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Subjects:
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Source:Am J Obstet Gynecol. 211(4):354.e1-354.e6
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Pubmed ID:24813971
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Pubmed Central ID:PMC4386593
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Document Type:
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Funding:
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Volume:211
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Issue:4
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Collection(s):
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Main Document Checksum:urn:sha256:1644acb8b4ef71e7cccdaa7964c2d02b652731226ece7487472b9ebd9ab9c097
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Download URL:
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File Type:
Supporting Files
File Language:
English
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