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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Comparison of HPV and cytology triage algorithms for women with borderline or mild dyskaryosis in population-based cervical screening (VUSA-screen study).
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Comparison of HPV and cytology triage algorithms for women with borderline or mild dyskaryosis in population-based cervical screening (VUSA-screen study).

机译:在基于人群的宫颈筛查(VUSA筛查研究)中,对于边缘性或轻度旋律不稳的女性,HPV和细胞学分类诊断算法的比较。

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摘要

We studied the effectiveness of high-risk human papillomavirus (hrHPV) triage for immediate colposcopy in women with borderline or mild dyskaryosis (BMD). In the Utrecht province of the Netherlands, women aged 30-60 years who participated in the regular cervical screening programme were offered hrHPV testing and cytology (intervention group) or cytology only (control group). In the intervention group (n = 337), women with BMD were immediately referred for colposcopy only if the sample was hrHPV positive. Women with a hrHPV negative test were advised to repeat cytology at 6 and 18 months and were referred for colposcopy if and when the repeat test result was positive (BMD or worse). In the control group (n = 329), referral of women with BMD was delayed until cytology was repeatedly positive at 6 or 18 months. The CIN3 detection rates were 10.7% (36/337) in the intervention group and 6.4% (21/329) in the control group (p = 0.047). Moreover, hrHPV triaging resulted in shorter time to diagnosis (154 vs. 381 days). Although the number of colposcopy referrals was 51.5% higher in the intervention group than in the control group, the medical costs per detected CIN3 were slightly lower ([euro] 4781 vs. [euro] 6235). If, in addition, hrHPV negative women had been referred back to routine screening at baseline, the CIN3 rate would have been 10.1% (34/337) and colposcopy rate would only have been 30.4% higher than in the control group. This study shows that hrHPV triaging of women with BMD is at least as effective for detecting CIN3 as repeat cytology, also when hrHPV negative women are referred back to routine screening.
机译:我们研究了高危型人乳头瘤病毒(hrHPV)分型对边缘性或轻度旋律不稳(BMD)妇女立即进行阴道镜检查的有效性。在荷兰的乌得勒支省,为参加常规宫颈筛查计划的30-60岁妇女提供了hrHPV检测和细胞学检查(干预组)或仅接受细胞学检查(对照组)。在干预组(n = 337)中,仅当hrHPV阳性样本时,才立即将BMD女性转诊接受阴道镜检查。建议hrHPV阴性测试的妇女在6和18个月时重复细胞学检查,如果重复测试结果为阳性(BMD或更差),则应进行阴道镜检查。在对照组(n = 329)中,BMD妇女的转诊被推迟,直到细胞学在6或18个月反复阳性。干预组的CIN3检测率是10.7%(36/337),对照组是6.4%(21/329)(p = 0.047)。此外,hrHPV分诊可缩短诊断时间(154天与381天)。尽管干预组的阴道镜检查转诊次数比对照组高51.5%,但每个检测到的CIN3的医疗费用略低(4781欧元对6235欧元)。此外,如果hrHPV阴性的妇女在基线被转回常规筛查,则CIN3率将为10.1%(34/337),阴道镜检查率仅比对照组高30.4%。这项研究表明,hrHPV分型对BMD妇女的检测CIN3至少与重复细胞学检查一样有效,而且当hrHPV阴性妇女返回常规筛查时也是如此。

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