Webb Sophie, Mat Ali Nafeesa, Sawyer Amy, Clark David J, Brown Megan A, Augustin Yolanda, Woo Yin Ling, Khoo Su Pei, Hargreaves Sally, Staines Henry M, Krishna Sanjeev, Hayes Kevin
Clinical Academic Group in Institute for Infection & Immunity, St George's University of London, London, United Kingdom.
St George's University Hospitals NHS Foundation Trust, London, United Kingdom.
PLOS Glob Public Health. 2024 May 23;4(5):e0003186. doi: 10.1371/journal.pgph.0003186. eCollection 2024.
Low vaginal self-sampling has been pioneered as an important development to improve uptake of cervical screening globally. Limited research is available in specific patient groups in the UK exploring views around self-sampling to detect high-risk human papillomavirus (hrHPV) DNA. Therefore, we explored patient views to support development of a novel point-of-care self-sampling cervical cancer screening device, by undertaking a cross-sectional semi-structured questionnaire survey to explore preferences, acceptability, barriers and facilitators around self-sampling. Patients attending a colposcopy clinic, 25-64 years old, were invited to participate after having carried out a low vaginal self-sample using a regular flocked swab. Participants self-completed an anonymous 12-point questionnaire. Quantitative data were analysed in MS Excel and Graphpad Prism, and qualitative data with Nvivo. We recruited 274 patients with a questionnaire response rate of 76%. Acceptability of self-sampling was high (95%, n = 187/197; Cronbachs-α = 0.778). Participants were asked their choice of future screening method: a) low vaginal self-sampling, b) healthcare professional collected vaginal swab, c) cervical brush sample with healthcare professional speculum examination, or d) no preference. Preferences were: a) 37% (n = 74/198), b) 19% (n = 37/198); c) 9% (n = 17/198), and d) 35% (n = 70/198), showing no single option as a strong preference. Key motivators were: Test simplicity (90%, n = 170/190), speed (81%, n = 153/190) and less pain (65%, n = 123/190). Barriers included lack of confidence taking the sample (53%, n = 10/19), resulting in preference for a healthcare professional sample (47%, n = 9/19). Whilst self-sampling showed high acceptability, lack of strong preference for screening method may reflect that respondents attending colposcopy are already engaged with screening and have differing perception of cervical cancer risk. This group appear less likely to 'switch' to self-sampling, and it may be better targeted within primary and community care, focusing on under-screened populations. Any shift in this paradigm in the UK requires comprehensive education and support for patients and providers.
低位阴道自我采样作为一项重要进展,已率先在全球范围内推动了子宫颈癌筛查的普及。在英国,针对特定患者群体围绕自我采样检测高危型人乳头瘤病毒(hrHPV)DNA的研究有限。因此,我们通过开展一项横断面半结构式问卷调查,以探究自我采样的偏好、可接受性、障碍和促进因素,从而探索患者的观点,以支持一种新型即时护理自我采样宫颈癌筛查设备的研发。邀请年龄在25至64岁之间、前往阴道镜检查门诊就诊的患者,在使用常规植绒拭子进行低位阴道自我采样后参与研究。参与者自行填写一份12项的匿名问卷。定量数据在MS Excel和Graphpad Prism中进行分析,定性数据则使用Nvivo进行分析。我们招募了274名患者,问卷回复率为76%。自我采样的可接受性较高(95%,n = 187/197;克朗巴哈α系数 = 0.778)。我们询问参与者对未来筛查方法的选择:a)低位阴道自我采样,b)医护人员采集的阴道拭子,c)医护人员使用窥器检查时采集的宫颈刷样本,或d)无偏好。偏好情况为:a)37%(n = 74/198),b)19%(n = 37/198);c)9%(n = 17/198),d)35%(n = 70/198),没有一种选择被强烈偏好。主要的推动因素包括:检测简便(90%,n = 170/190)、速度快(81%,n = 153/190)和疼痛轻(65%,n = 123/190)。障碍包括对采集样本缺乏信心(53%,n = 10/19),导致更倾向于由医护人员采样(47%,n = 9/19)。虽然自我采样显示出较高的可接受性,但对筛查方法缺乏强烈偏好可能反映出,前往阴道镜检查门诊就诊的受访者已经参与了筛查,并且对宫颈癌风险有不同的认知。这一群体似乎不太可能“转向”自我采样,或许在初级和社区护理中针对筛查不足的人群进行推广会更好。在英国,这种模式的任何转变都需要对患者和提供者进行全面的教育和支持。