Evaluation of a novel vaginal cells self‐sampling device for human papillomavirus testing in cervical cancer screening: A clinical trial assessing reliability and acceptability

Author:

Yang Chung‐Yao1ORCID,Chang Ting‐Chang23,Chou Hung‐Hsueh234,Chao Angel23,Hsu Shih‐Tien5,Shih Yu‐Hsiang5,Huang Huei‐Jean23,Lin Cheng‐Tao23,Chen Min‐Yu23,Sun Lou5,Huang Kuan‐Gen23,Wu Kai‐Yun2,Hsieh Wu‐Chiao2,Huang Yi‐Ting2,Chen Liang‐Hsuan2,Lu Chien‐Hsing5,Lin Hao6,Cheng Chao‐Min7ORCID

Affiliation:

1. Hygeia Touch Inc. Taipei Taiwan

2. Division of Gynecologic Oncology, Department of Obstetrics and Gynecology Chang Gung Memorial Hospital, Linkou Branch Taoyuan Taiwan

3. Gynecologic Cancer Research Center, Chang Gung Memorial Hospital Taoyuan Taiwan

4. School of Medicine, National Tsing Hua University Hsinchu Taiwan

5. Department of Gynecology and Obstetrics Taichung Veterans General Hospital Taichung Taiwan

6. Department of Obstetrics and Gynecology Kaohsiung Chang Gung Memorial Hospital Kaohsiung Taiwan

7. Institute of Biomedical Engineering, National Tsing Hua University Hsinchu Taiwan

Abstract

AbstractCervical cancer is a significant public health concern, particularly in low‐ and middle‐income countries where resources for prevention and treatment are limited. Routine screening, such as the Papanicolaou test (Pap smears) and human papillomavirus (HPV) testing, plays a crucial role in the early detection and prevention of cervical cancer. However, the participation rate in cervical cancer screening programs remains below optimal levels due to various factors. This study aimed to evaluate the reliability and acceptability of the HygeiaTouch Self Sampling Kit for Women in collecting vaginal samples for HPV typing, comparing the results with samples collected by physicians. The study included 1210 women aged 21–65 from three medical centers in Taiwan. The findings indicated that the self‐sampling kit was as effective as physician‐collected specimens in terms of obtaining valid samples and identifying HPV. The agreement between the two methods was 88%, with a κ value of 0.75. Furthermore, the study assessed the mechanical characteristics of the self‐sampling applicator through tensile, bending, and torque tests, and determined that it was safe for intravaginal use. Additionally, the study evaluated the safety and satisfaction of self‐sampling and found a low rate of adverse events (0.7%) and high levels of satisfaction (over 90%) among participants. Overall, we demonstrated that the HygeiaTouch Self Sampling Kit for Women is a reliable and acceptable device for HPV testing and cervical screening, providing a convenient, safe, and effective alternative for women.

Publisher

Wiley

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