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阴道镜检查门诊患者对人乳头瘤病毒阴道自我采样的接受度

Acceptability of Vaginal Human Papillomavirus Self-Collection Among Colposcopy Clinic Attendees.

作者信息

MacLaughlin Kathy L, Cole Kristin C, Maxson Julie A, McCann Jainnee, Zhu Xuan, Jacobson Robert M, Meunier Matthew R, Long Margaret E

机构信息

Department of Family Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

Womens Health Rep (New Rochelle). 2025 Apr 14;6(1):421-430. doi: 10.1089/whr.2025.0006. eCollection 2025.

Abstract

BACKGROUND

Cervical cancer screening with a self-collected vaginal specimen for human papillomavirus (HPV) testing was approved by the U.S. Food and Drug Administration in May 2024, offering a potential solution to declining screening rates.

OBJECTIVE

We aimed to assess acceptability of clinic-based vaginal specimen self-collection for HPV testing and to evaluate associations between participants' sociodemographics and their likelihood of choosing self-collection for future screening and the overall acceptability of using the Evalyn® brush device. We also evaluated associations between specific acceptability constructs and reported likelihood to use the device in the future and overall acceptability.

METHODS

Following self-collection of a vaginal specimen, participants completed an electronic survey that measured constructs from the Theoretical Framework of Acceptability. Associations were assessed using logistic regressions. The study was conducted at a colposcopy clinic in the Gynecology department of a midwestern academic medical center in the United States from November 2022 through July 2023.

RESULTS

Participants ( = 81) reported high likelihood (98% likely or very likely) of choosing in-home self-collection for future screening and unanimity on overall acceptability (100% acceptable or completely acceptable) of using the device. More affirmative responses to measures on instruction understandability, ease of device use, understanding the device is used for cervical cancer screening, and perceiving self-collection improves screening rates were associated with a higher likelihood to choose self-collection for future screenings and overall acceptability of the device (all values <0.05).

CONCLUSION

Vaginal specimen self-collection for HPV testing was well-received in the studied population, with high acceptability and likelihood of uptake. Implementation efforts should provide user-friendly instructions and emphasize the benefits of self-collection for cervical cancer screening, particularly among people less likely to engage with clinician-collected speculum-based screening.

摘要

背景

2024年5月,美国食品药品监督管理局批准使用自行采集的阴道样本进行人乳头瘤病毒(HPV)检测以进行宫颈癌筛查,这为筛查率下降提供了一个潜在的解决方案。

目的

我们旨在评估基于诊所的阴道样本自行采集用于HPV检测的可接受性,并评估参与者的社会人口统计学特征与他们未来选择自行采集进行筛查的可能性以及使用Evalyn®刷具的总体可接受性之间的关联。我们还评估了特定可接受性结构与报告的未来使用该设备的可能性和总体可接受性之间的关联。

方法

在自行采集阴道样本后,参与者完成了一项电子调查,该调查测量了可接受性理论框架中的结构。使用逻辑回归评估关联。该研究于2022年11月至2023年7月在美国中西部一所学术医疗中心妇产科的阴道镜诊所进行。

结果

参与者(n = 81)报告称,未来筛查选择在家自行采集的可能性很高(98%可能或非常可能),并且对使用该设备的总体可接受性一致(100%可接受或完全可接受)。对关于指导理解性、设备使用便利性、理解设备用于宫颈癌筛查以及认为自行采集可提高筛查率的措施有更多肯定回答,与未来筛查选择自行采集的可能性更高以及设备的总体可接受性相关(所有P值<0.05)。

结论

在研究人群中,用于HPV检测的阴道样本自行采集受到好评,具有很高的可接受性和采用可能性。实施工作应提供用户友好的指导,并强调自行采集对宫颈癌筛查的益处,特别是在不太可能接受临床医生采集的窥阴器筛查的人群中。

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