Global Health Sciences, Clinton Health Access Initiative, Boston, Massachusetts, USA
Global Diagnostics Team, Clinton Health Access Initiative, Boston, Massachusetts, USA.
BMJ Open. 2023 Jan 6;13(1):e065074. doi: 10.1136/bmjopen-2022-065074.
To demonstrate acceptability and operational feasibility of introducing human papillomavirus (HPV) testing as a principal cervical cancer screening method in public health programmes in sub-Saharan Africa.
45 primary and secondary health clinics in Malawi, Nigeria, Senegal, Uganda and Zimbabwe.
15 766 women aged 25-54 years presenting at outpatient departments (Senegal only, general population) or at antiretroviral therapy clinics (all other countries, HIV-positive women only). Eligibility criteria followed national guidelines for cervical cancer screening.
HPV testing was offered to eligible women as a primary screening for cervical cancer, and HPV-positive women were referred for visual inspection with acetic acid (VIA), and if lesions identified, received treatment or referral.
The primary outcomes were the proportion of HPV-positive women who received results and linked to VIA and the proportion of HPV-positive and VIA-positive women who received treatment.
A total of 15 766 women were screened and tested for HPV, among whom 14 564 (92%) had valid results and 4710/14 564 (32%) were HPV positive. 13 837 (95%) of valid results were returned to the clinic and 3376 (72%) of HPV-positive women received results. Of women receiving VIA (n=2735), 715 (26%) were VIA-positive and 622 (87%) received treatment, 75% on the same day as VIA.
HPV testing was found to be feasible across the five study countries in a public health setting, although attrition was seen at several key points in the cascade of care, namely results return to women and linkage to VIA. Once women received VIA, if eligible, the availability of on-site cryotherapy and thermal ablation allowed for same-day treatment. With sufficient resources and supportive infrastructure to ensure linkage to treatment, use of HPV testing for cervical cancer screening as recommended by WHO is a promising model in low-income and middle-income countries.
展示在撒哈拉以南非洲的公共卫生项目中引入人乳头瘤病毒(HPV)检测作为宫颈癌筛查主要方法的可接受性和操作可行性。
马拉维、尼日利亚、塞内加尔、乌干达和津巴布韦的 45 个初级和二级保健诊所。
15766 名年龄在 25-54 岁的妇女,她们在门诊部就诊(仅在塞内加尔,为普通人群;或在抗逆转录病毒治疗诊所就诊(所有其他国家,为 HIV 阳性妇女)。符合条件的妇女符合国家宫颈癌筛查指南。
向符合条件的妇女提供 HPV 检测作为宫颈癌的主要筛查方法,HPV 阳性妇女被转诊进行醋酸视觉检查(VIA),如果发现病变,则接受治疗或转诊。
主要结果是接受结果并与 VIA 相关联的 HPV 阳性妇女的比例,以及 HPV 阳性和 VIA 阳性妇女接受治疗的比例。
共有 15766 名妇女接受了 HPV 筛查和检测,其中 14564 名(92%)有有效结果,4710 名(32%)HPV 阳性。13837 名(95%)有效结果返回诊所,3376 名(72%)HPV 阳性妇女收到结果。在接受 VIA(n=2735)的妇女中,715 名(26%)VIA 阳性,622 名(87%)接受治疗,75%在 VIA 当天进行。
在五个研究国家的公共卫生环境中,HPV 检测被证明是可行的,尽管在护理过程的几个关键点上存在流失,即结果返回给妇女和与 VIA 的联系。一旦妇女接受了 VIA,如果符合条件,现场提供的冷冻疗法和热消融术允许当天进行治疗。有足够的资源和支持性基础设施来确保与治疗的联系,因此按照世卫组织的建议,将 HPV 检测用于宫颈癌筛查是低收入和中等收入国家的一种有前途的模式。