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• W4312019711 abstract "Self-sampling human papillomavirus (HPV) testing has been introduced for cervical cancer screening worldwide. In Japan, there are two types (brush and sponge) of HPV self-sampling devices. However, the recommended type for cervical cancer screening remains unclear. This study aimed to evaluate the feasibility of the HPV self-sampling device-sponge type (HSD-ST). Additionally, we aimed to examine the positive rate (sensitivity) for cervical intraepithelial neoplasia (CIN) 2 or worse using the HSD-ST. Finally, we aimed to perform a questionnaire survey regarding the usability of the HSD-ST.We included 165 women who underwent HPV testing at one of three gynecologic clinics. First, the women used the HSD-ST and completed a questionnaire regarding its usability. Subsequently, they underwent physician-sampling HPV testing and cytology. We examined the agreement rate of HPV positivity between self- and physician-sampling HPV testing.The HPV-positive rates of self- and physician-collected samples were 59.4% and 62.4%, respectively, with an overall concordance rate of 88.5% and a calculated kappa coefficient of 0.76, indicating high concordance. Moreover, the positive (sensitivity) rates for CIN2 or worse were 81.4% and 89.8% in the self- and physician-collected samples, respectively.Our findings demonstrated the feasibility and usability of the HSD-ST." @default.
• W4312019711 created "2023-01-03" @default.
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• W4312019711 date "2022-12-15" @default.
• W4312019711 modified "2023-10-18" @default.
• W4312019711 title "Evaluation of the feasibility of human papillomavirus sponge‐type self‐sampling device at Japanese colposcopy clinics" @default.
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• W4312019711 doi "https://doi.org/10.1111/jog.15496" @default.
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• W4312019711 hasPublicationYear "2022" @default.
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