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- Chris L. McGowin, PhD⇑
- Rodney E. Rohde, PhD, MS, SV, SM(ASCP)CM, MBCM
- Gerald Redwine, MEd, MT(ASCP)
- Address for Correspondence: Chris L. McGowin, PhD, Louisiana State University Health Sciences Center, Department of Microbiology, Immunology and Parasitology, 1901 Perdido St.; MEB 6214, New Orleans, LA 70112-2822, 504 568-7281, cmcgow{at}lsuhsc.edu
Discuss the historical and epidemiological background of Human Papilloma Virus (HPV) infections.
Define current evidence based guidelines for HPV diagnosis and management
Justify the epidemiological and clinical rationale for HPV testing in the management of cervical cancer
Extract
Human Papilloma Virus (HPV) is the most common sexually transmitted infection (STI), and currently is the only vaccine-preventable etiology of urogenital disease. As an STI, HPV is an independent risk factor for virtually all cases of cervical cancer and is associated with anogenital and orolabial warts. Importantly, infection with HPV is a necessary factor in the development of squamous cervical neoplasia despite the fact that most infections and dysplastic abnormalities will not progress to malignant transformation.1-3 Over 100 genotypes of HPV have been identified of which less than 50% are transmitted sexually.4 Of the urogenital HPV types, several have been associated directly with the enhanced risk of cervical cancer.4 In 2012, updated guidelines for cervical cancer screening were put forth by the US Preventative Services Task Force (USPSTF) and the combined partnership of the American Society for Colposcopy and Cervical Pathology (ASCCP), the American Cancer Society (ACS) and the American Society for Clinical Pathology (ASCP). Collectively these guidelines lengthened the time interval between cervical cancer screens and increased the age to begin screening. These evidence-based recommendations indicate the use of either cytology alone or in combination with an FDA-approved HPV test stratified primarily by age, but also by the interval since last screen and hysterectomy status. Compared to cytological investigation alone, co-testing can more informatively direct the need for and method of treating precancerous lesions by more accurately assessing a woman's risk for developing cancer. This article aims to concisely summarize the current guidelines for managing cervical cancer screening, and…
ABBREVIATIONS: ACS - American Cancer Society, ASCP - American Society for Clinical Pathology, ASCCP - American Society for Colposcopy and Cervical Pathology, ASCUS - atypical squamous cells of undetermined significance, CIN - cervical intraepithelial neoplasia, FDA - Food and Drug Administration, HPV - Human Papilloma Virus, HR-HPV - high-risk HPV, HSIL - high-grade squamous intraepithelial lesions, LSIL - low-grade squamous intraepithelial lesions, MDx - molecular diagnostics, NAAT - nucleic acid amplification test, NPV - negative predictive value, PPV - positive predictive value, STD - sexually transmitted disease, STI - sexually transmitted infection.
- INDEX TERMS
- Molecular diagnostics
- HPV
- Human Papilloma Virus
- sexually transmitted disease
- sexually transmitted infection
- cervical cancer
- co-testing
- nucleic acid amplification test
- NAAT
Discuss the historical and epidemiological background of Human Papilloma Virus (HPV) infections.
Define current evidence based guidelines for HPV diagnosis and management
Justify the epidemiological and clinical rationale for HPV testing in the management of cervical cancer
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