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瑞典评分法的阴道镜评估,在瑞典筛查计划中的效果评估:一项横断面研究。

Colposcopic assessment by Swedescore, evaluation of effectiveness in the Swedish screening programme: a cross-sectional study.

机构信息

Department of Obstetrics and Gynaecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Regional Cancer Centre West, Gothenburg, Sweden.

出版信息

BJOG. 2022 Jul;129(8):1261-1267. doi: 10.1111/1471-0528.17054. Epub 2021 Dec 30.

Abstract

OBJECTIVE

To evaluate the effectiveness and performance of Swedescore in the Swedish screening programme.

DESIGN

Cross-sectional register study.

SETTING AND POPULATION

All Swedish women aged over 18 years with a colposcopic assessment linked to a biopsy in the Swedish National Cervical Screening Registry, 2015-20.

METHODS

Colposcopies with Swedescore were compared with the histopathological diagnosis of cervical intraepithelial neoplasia grade 2 or higher (CIN2+). The respective influence of cytology and human papillomavirus (HPV) testing, at referral for colposcopy and concurrently with colposcopy, were investigated in regression models.

MAIN OUTCOME MEASURES

CIN2+.

RESULTS

A total of 11 317 colposcopic assessments with Swedescore were included. Odds ratios for CIN2+ increased for every step in the Swedescore scale. At Swedescore ≥0-1, the proportion of CIN2+ was 9.8%. At Swedescore ≥8, the specificity was 93.3% and the positive predictive value was 60.1%, Area under the receiver operating characteristics curve (AUC) was 0.71. If the smear had been abnormal at referral, a normal colposcopy (Swedescore 0-1) was still associated with a CIN2+ risk of more than 5%. In the regression model, cytology and HPV had higher odds ratio for CIN2+ than colposcopy; the combination resulted in an AUC of 0.88.

CONCLUSIONS

Swedescore works well in a routine clinical setting but colposcopy assessed with Swedescore was inferior to that reported in previous clinical studies. No safe cutoff level was identified for refraining from biopsy. See-and-treat at Swedescore 8-10 is feasible only if referral cytology showed high-grade squamous intraepithelial lesion.

TWEETABLE ABSTRACT

No safe cutoff level for refraining from biopsy nor for see-and-treat with Swedescore.

摘要

目的

评估 Swedescore 在瑞典筛查计划中的有效性和表现。

设计

横断面登记研究。

设置和人群

所有年龄在 18 岁以上的瑞典女性,在瑞典国家宫颈筛查登记处有阴道镜评估并伴有活检,时间为 2015-20 年。

方法

比较 Swedescore 阴道镜与宫颈上皮内瘤变 2 级或更高级别(CIN2+)的组织病理学诊断。在回归模型中,调查了细胞学和人乳头瘤病毒(HPV)检测在转诊阴道镜检查时和同时进行时的各自影响。

主要观察指标

CIN2+。

结果

共纳入 11317 例 Swedescore 阴道镜检查。Swedescore 量表每增加一个等级,CIN2+的比值比就会增加。在 Swedescore≥0-1 时,CIN2+的比例为 9.8%。在 Swedescore≥8 时,特异性为 93.3%,阳性预测值为 60.1%,接受者操作特征曲线下面积(AUC)为 0.71。如果转诊时涂片异常,正常阴道镜检查(Swedescore 0-1)仍与 CIN2+风险超过 5%相关。在回归模型中,细胞学和 HPV 对 CIN2+的比值比高于阴道镜检查;两者结合的 AUC 为 0.88。

结论

Swedescore 在常规临床环境中效果良好,但用 Swedescore 评估的阴道镜检查不如以前的临床研究报道的效果好。没有确定活检的安全截止水平。仅在转诊细胞学显示高级别鳞状上皮内病变时,Swedescore 8-10 的“见病变即治疗”才可行。

研究意义

没有活检的安全截止水平,也没有 Swedescore 的“见病变即治疗”的安全截止水平。

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