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在转诊行阴道镜检查的女性中,与由临床医生采集的宫颈样本相比,自行采集的阴道和尿液样本用于 HPV 检测的临床性能和可接受性。一项横断面研究。

Clinical performance and acceptability of self-collected vaginal and urine samples compared with clinician-taken cervical samples for HPV testing among women referred for colposcopy. A cross-sectional study.

机构信息

Clinical Pathology, Sygehus Lillebalt Vejle Sygehus, Vejle, Denmark

Department of Gynecology, Odense University Hospital, Odense, Denmark.

出版信息

BMJ Open. 2021 Mar 5;11(3):e041512. doi: 10.1136/bmjopen-2020-041512.

Abstract

OBJECTIVES

To increase effectiveness of the cervical cancer screening program, self-sampling can be an option. Both self-collected vaginal samples (SCV) and urine samples may be useful alternatives to clinician-taken cervical samples (CS).

DESIGN

Cross-sectional study.

SETTING

Colposcopy clinic.

PARTICIPANTS

Women (n=305) referred to colposcopy after abnormal cervical screening result or conditions like postcoital bleeding.

INTERVENTION

All women self-collected a urine and a vaginal sample prior to colposcopy, where a CS and biopsies were taken. All samples were tested for high-risk human papillomavirus (HPV) using the Cobas HPV assay. The gold standard was histology diagnoses (CIN2+/CIN3+) from biopsies obtained at the same examination.

PRIMARY OUTCOME

Absolute and relative sensitivity and specificity of HPV testing on SCV and urine to detect CIN2+/CIN3+ compared with the CS.

SECONDARY OUTCOME

The acceptability by women of self-sampling.

RESULTS

Both the vaginal and urine sample were comparable to the CS in identifying severe intraepithelial neoplasia (CIN2+/CIN3+). Absolute sensitivity ranged from 93% for urine samples to 96% for SCV for detecting CIN2+, which is comparable to the sensitivity of CS (overlapping 95% CI).The relative sensitivity for detecting CIN2+ was 1.00 (95% CI 0.96 to 1.04) for SCV and 0.96 (95% CI 0.91 to 1.03) for urine samples. At CIN3+, the relative sensitivity was 1.00 (95% CI 0.96 to 1.08) and 0.97 (95% CI 0.89 to 1.07) for SCV and urine samples, respectively. There were no statistical differences between the self-collected samples and the CS (McNemar's test >0.05). The relative specificity was also similar (1.03 (95% CI 0.95 to 1.12) for SCV and 0.98 (95% CI 0.89 to 1.09) for urine samples) (McNemar's test >0.05).The acceptability of self-sampling was evaluated by questionnaire. The women found the instructions on sample collection easy to understand and were positive about self-sampling with a preference for the urine sample.

CONCLUSION

Self-sampling by SCV and urine is a clinically safe alternative to CS with a high degree of acceptability.

摘要

目的

为了提高宫颈癌筛查计划的效果,自我采样可以作为一种选择。自我采集的阴道样本(SCV)和尿液样本都可能是替代临床医生采集宫颈样本(CS)的有用方法。

设计

横断面研究。

地点

阴道镜诊所。

参与者

305 名因宫颈筛查异常或接触后出血等情况转诊至阴道镜检查的女性。

干预措施

所有女性在阴道镜检查前自行采集尿液和阴道样本,同时采集 CS 和活检样本。所有样本均采用 Cobas HPV 检测试剂盒检测高危型人乳头瘤病毒(HPV)。金标准是活检诊断为(CIN2+/CIN3+)。

主要结果

比较 CS,HPV 检测 SCV 和尿液样本对 CIN2+/CIN3+的绝对和相对敏感性和特异性。

次要结果

女性对自我采样的接受程度。

结果

阴道和尿液样本在识别严重上皮内瘤变(CIN2+/CIN3+)方面与 CS 相当。检测 CIN2+的绝对敏感性范围从尿液样本的 93%到 SCV 的 96%,与 CS 的敏感性相当(重叠 95%可信区间)。SCV 检测 CIN2+的相对敏感性为 1.00(95%可信区间 0.96 至 1.04),尿液样本为 0.96(95%可信区间 0.91 至 1.03)。在 CIN3+方面,SCV 和尿液样本的相对敏感性分别为 1.00(95%可信区间 0.96 至 1.08)和 0.97(95%可信区间 0.89 至 1.07)。自我采集样本与 CS 之间无统计学差异(McNemar 检验>0.05)。相对特异性也相似(SCV 为 1.03(95%可信区间 0.95 至 1.12),尿液样本为 0.98(95%可信区间 0.89 至 1.09)(McNemar 检验>0.05)。通过问卷调查评估了自我采样的可接受性。女性认为样本采集说明易于理解,并对自我采样持积极态度,更倾向于尿液样本。

结论

SCV 和尿液的自我采样是 CS 的一种安全替代方法,具有高度的可接受性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3aae/7939007/3ba7123201f5/bmjopen-2020-041512f01.jpg

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