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首页> 外文期刊>Preventive Medicine: An International Journal Devoted to Practice and Theory >High-risk human papillomavirus detection in self-sampling compared to physician-taken smear in a responder population of the Dutch cervical screening: Results of the VERA study
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High-risk human papillomavirus detection in self-sampling compared to physician-taken smear in a responder population of the Dutch cervical screening: Results of the VERA study

机译:在荷兰宫颈筛查的响应人口中的医生涂片相比,自我抽样中高风险的人乳头瘤病毒检测:VERA研究的结果

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Abstract In 2017 the cervical cancer screening program in The Netherlands will be revised. Cervical smears will primarily be tested for the presence of high-risk human papillomavirus (hrHPV) instead of cytology, and vaginal self-sampling will be offered to non-responders. This includes a potential risk that part of the women who would otherwise opt for a cervical smear will wait for self-sampling. However, self-sampling for hrHPV in a responder population has never been studied yet. The aim of this study was to investigate the applicability and accuracy of self-sampling in detecting hrHPV in a screening responder population. A total of 2049 women, aged 30–60 years, participating in the screening program in The Netherlands were included from April 2013 to May 2015. After they had their cervical smear taken, women self-collected a cervicovaginal sample with a brush-based device, the Evalyn Brush. Both the cervical smear and self-sample specimen were tested with the COBAS 4800 HPV platform. The hrHPV prevalence was 8.0% (95% CI 6.9–9.2) among the physician-taken samples, and 10.0% (95% CI 8.7–11.3) among the self-samples. There was 96.8% (95% CI 96.0–97.5) concordance of hrHPV prevalence between self-samples and physician-taken samples. Women in our study evaluated self-sampling as convenient (97.1%), user-friendly (98.5%), and 62.8% preferred self-sampling over a physician-taken sampling for the next screening round. In conclusion, self-sampling showed high concordance with physician-taken sampling for hrHPV detection in a responder screening population and highly acceptable to women. Implementation of HPV-self-sampling for the responder population as a primary screening tool may be considered. Highlights ? Self-sampling for a hrHPV based cervical screening program ? Investigate applicability and accuracy of hrHPV self-sampling in a responder population ? 96.8% hrHPV concordance between self-samples and physician-taken samples ? 62.8% preferred self-sampling over a cervical smear for the next screening round ]]>
机译:摘要2017年荷兰宫颈癌筛查计划将被修订。宫颈涂片主要用于高危人乳头瘤病毒(HRHPV)而不是细胞学的存在,而阴道自抽样将提供给非响应者。这包括潜在的风险,这些潜在风险将否则选择宫颈涂片的女性将等待自我抽样。但是,答复人口中HRHPV的自我抽样尚未研究。本研究的目的是探讨在筛选响应人口中检测HRHPV的自我抽样的适用性和准确性。在2013年4月至2015年5月,共有2049岁的女性参加荷兰的筛选计划。在他们患有颈椎涂片后,妇女用基于刷子的装置自我收集了颈椎动物样品,Evalyn刷子。用COBAS 4800 HPV平台测试宫颈涂片和自样标本。 HRHPV患病率为8.0%(95%CI 6.9-9.2),在自我样本中,10.0%(95%CI 8.7-11.3)。有96.8%(95%CI 96.0-97.5)的HRHPV在自我样本和医生采样的样品之间的一致性。我们研究中的妇女评估了自适应,方便(97.1%),用户友好(98.5%),62.8%优先于医生采样,用于下一个筛选圆形。总之,自我抽样表明,在响应者筛选人口中的HRHPV检测中对HRHPV检测进行了高度的一致性,并且对女性的高度可接受。可以考虑作为主要筛查工具的响应者群体的HPV自抽样的实现。强调 ?基于HRHPV的宫颈筛查计划的自我抽样?调查响应者人口中HRHPV自抽样的适用性和准确性? 96.8%HRHPV在自我样本和医生采样之间的一致性? 62.8%优选在颈部涂片上的优选自抽样,用于下一个筛选圆形]]>

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