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Reduction in Human Papillomavirus (HPV) Prevalence Among Young Women Following HPV Vaccine Introduction in the United States, National Health and Nutrition Examination Surveys, 2003–2010

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TLDR
Within 4 years of vaccine introduction, the vaccine-type HPV prevalence decreased among females aged 14-19 years despite low vaccine uptake, and the estimated vaccine effectiveness was high.
Abstract
Background. Human papillomavirus (HPV) vaccination was introduced into the routine immunization schedule in the United States in late 2006 for females aged 11 or 12 years with catch-up vaccination recommended for those aged 13-26 years. In 2010 3-dose vaccine coverage was only 32% among 13-17 year-olds. Reduction in the prevalence of HPV types targeted by the quadrivalent vaccine (HPV-6 -11 -16 and -18) will be one of the first measures of vaccine impact. Methods. We analyzed HPV prevalence data from the vaccine era (2007-2010) and the prevaccine era (2003-2006) that were collected during National Health and Nutrition Examination Surveys. HPV prevalence was determined by the Linear Array HPV Assay in cervicovaginal swab samples from females aged 14-59 years; 4150 provided samples in 2003-2006 and 4253 provided samples in 2007-2010. Results. Among females aged 14-19 years the vaccine-type HPV prevalence (HPV-6 -11 -16 or -18) decreased from 11.5% (95% confidence interval [CI] 9.2-14.4) in 2003-2006 to 5.1% (95% CI 3.8-6.6) in 2007-2010 a decline of 56% (95% CI 38-69). Among other age groups the prevalence did not differ significantly between the 2 time periods (P > .05). The vaccine effectiveness of at least 1 dose was 82% (95% CI 53-93). Conclusions. Within 4 years of vaccine introduction the vaccine-type HPV prevalence decreased among females aged 14-19 years despite low vaccine uptake. The estimated vaccine effectiveness was high.

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Personalized Decision Modeling for Intervention and Prevention of Cancers

Fan Wang
TL;DR: The findings suggest that personalized screening and vaccination benefit patients by maximizing life expectancies and minimizing the possibilities of dying from cancer.
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HPV vaccination in women treated for CIN2/3: it's still all about prevention.

TL;DR: Interestingly, despite the absence of randomization, the vaccination and non-vaccination groups were remarkably well balanced in regards to age, disease status at LEEP, margin status, and baseline HPV 16 and 18positivity.
Journal ArticleDOI

İnsan Papilloma Virüsü (HPV) ve Aşılarının Kullanımı Sonrası Toplumsal Etkileri

TL;DR: Ayrıca enfekte olan kişilerde uzun süre herhangi bir belirti olmasa da virüsün vücuttaki yaşam döngüsusü devam edebilmektedir ve uzuun vadede kanser gelişimine neden olabilmekaertir as mentioned in this paper .
References
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Journal ArticleDOI

A review of human carcinogens--Part B: biological agents

TL;DR: In this paper, the carcinogenicity of the biological agents classifi ed as "carcinogenic to humans" (Group 1) and to identify additional tumour sites and mechanisms of carcinogenesis (tables 1 and 2).
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Human papillomavirus genotype attribution in invasive cervical cancer: a retrospective cross-sectional worldwide study

Silvia de Sanjosé, +62 more
- 01 Nov 2010 - 
TL;DR: HPV types 16, 18, 31, 33, 35, 45, 52, and 58 should be given priority when the cross-protective effects of current vaccines are assessed, and for formulation of recommendations for the use of second-generation polyvalent HPV vaccines, according to this largest assessment of HPV genotypes to date.
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Quadrivalent vaccine against human papillomavirus to prevent high-grade cervical lesions

TL;DR: In young women who had not been previously infected with HPV-16 or HPV-18, those in the vaccine group had a significantly lower occurrence of high-grade cervical intraepithelial neoplasia related to HPV- 16 or HPV -18 than did those inThe placebo group.
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