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首页> 外文期刊>Journal of lower genital tract disease. >Benchmarking CIN 3+ Risk as the Basis for Incorporating HPV and Pap Cotesting into Cervical Screening and Management Guidelines
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Benchmarking CIN 3+ Risk as the Basis for Incorporating HPV and Pap Cotesting into Cervical Screening and Management Guidelines

机译:将CIN 3+风险作为基准将HPV和子宫颈抹片检查纳入宫颈筛查和管理指南

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Objective. In 2012, the US Preventive Services Task Force (USPSTF) and a consensus of 25 organizations endorsed concurrent cytology and human papillomavirus (HPV) testing ("cotesting") for cervical cancer screening. Past screening and management guidelines were implicitly based on risks defined by Pap-alone, without consideration of HPV test results. To promote management that is consistent with accepted practice, new guidelines incorporating cotesting should aim to achieve equal management of women at equal risk of cervical intraepithelial neoplasia grade 3 and cancer (CIN 3+).Methods. We estimated cumulative 5-year risks of CIN 3+ for 965,360 women aged 30 to 64 years undergoing cotesting at Kaiser Permanente Northern California over 2003 to 2010. We calculated the implicit risk thresholds for Pap-alone and applied them for new management guidance on HPV and Pap cotesting, citing 2 examples: HPV-positive/atypical squamous cells of undetermined significance (ASC-US) and HPV-negative/Pap-negative. We call this guidance process "benchmarking."Results. A low-grade squamous intraepithelial lesion result, for which immediate colposcopy is prescribed, carries a 5-year CIN 3+ risk of 5.2%, suggesting that test results with similar risks should be managed with colposcopy. Similarly, ASC-US (2.6% risk) is managed with a 6- to 12-month follow-up visit and Pap-negative (0.26% risk) is managed with a 3-year follow-up visit. The 5-year CIN 3+ risk among women with HPV-positive/ASC-US was 6.8% (95% confidence interval = 6.2%-7.6%). This is greater than the 5.2% risk implicitly leading to referral for colposcopy, consistent with current management recommendations that women with HPV-positive/ASC-US be referred for immediate colposcopy. The 5-year CIN 3+ risk among women with HPV-negative/Pap-negative results was 0.08% (95% confidence interval = 0.07%-0.09%), far below the 0.26% implicitly required for a 3-year return and justifying a longer (e.g., 5-year) return. Conclusions. Using the principle of "equal management of equal risks," benchmarking to implicit risk thresholds based on Pap-alone can be used to achieve safe and consistent incorporation of cotesting.
机译:目的。 2012年,美国预防服务工作队(USPSTF)和25个组织达成共识,同意同时进行细胞学检查和人类乳头瘤病毒(HPV)测试(“共同测试”)以筛查子宫颈癌。过去的筛查和管理指南隐含地基于仅由Pap定义的风险,而不考虑HPV测试结果。为了促进与公认的实践相一致的管理,纳入共测的新指南应旨在实现对患有宫颈上皮内瘤变3级和癌症(CIN 3+)的风险相同的女性进行平等管理。我们估算了2003年至2010年间,在965360名年龄在30至64岁的30至64岁女性中,在北加州凯撒永久医疗中心进行共同测试的5年累积累积风险。我们计算了单独使用Pap的隐含风险阈值,并将其应用于HPV的新管理指南和Pap共同测试,列举2个例子:意义不明的HPV阳性/非典型鳞状细胞(ASC-US)和HPV阴性/ Pap阴性。我们将此指导过程称为“基准测试”。结果。要求立即进行阴道镜检查的低度鳞状上皮内病变结果的5年CIN 3+风险为5.2%,这表明应通过阴道镜检查对具有类似风险的测试结果进行管理。同样,对ASC-US(2.6%的风险)进行6到12个月的随访,而对Pap阴性(0.26%的风险)进行3年的随访。 HPV阳性/ ASC-US女性的5年CIN 3+风险为6.8%(95%置信区间= 6.2%-7.6%)。这高于隐式导致接受阴道镜检查的5.2%风险,这与当前的管理建议一致,即HPV阳性/ ASC-US的女性应立即进行阴道镜检查。 HPV阴性/ Pap阴性结果的女性的5年CIN 3+风险为0.08%(95%置信区间= 0.07%-0.09%),远低于3年回报和证明理由所隐含的0.26%更长(例如5年)的回报。结论。使用“风险均等管理”的原则,可以基于仅基于Pap的基准对隐式风险阈值进行基准测试,以实现安全,一致地合并测试。

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