Public Health Research Institute of India, Mysore, Karnataka, India.
School of Public Health, Johns Hopkins University, Baltimore, Tucson, USA.
Indian J Cancer. 2021 Jul-Sep;58(3):409-416. doi: 10.4103/ijc.IJC_162_19.
Cervical cancer is the third most common cancer among women in India. The aim of the study is to determine the feasibility of using the Gynocular-triage-to-diagnose (Gynocular T2D/GT2D) in conjunction with visual inspection with acetic acid (VIA) in community-based cervical cancer screening programs in rural Mysore, India.
Between November 2015 and August 2016, the Public Health Research Institute of India (PHRII) implemented a mobile cervical cancer-screening in Mysore district using VIA and GT2D. Women underwent speculum exams and VIA positive cases were identified. Swede score was assessed using GT2D and a score >4 indicated further monitoring or referral for treatment. Papanicolaou (Pap) smears were conducted for selected cases. Statistical analysis was performed using Chi-square and Fisher's exact tests.
Among 199 women registered in the camp, 176 were included in the final analysis. 23 women were excluded due to vaginal bleeding. The average age of women was 39 years (range = 27-59 years). Among the 176 cases, 38 (21.6%) were VIA positive and 138 (78.4%) were VIA negative. Swede score of >4 was observed in 6 VIA positive and 7 VIA negative women. Two cases among VIA negative with a score of >4 were suggested biopsy.
Gynocular triaging prevented overtreatment of 32 (18.1%) participants, and identified 7 subjects with >4 Swede score even in VIA negative cases, which would have been ignored if VIA alone was used. In summary, our study demonstrates that Gynocular triaging is feasible in community cervical cancer screening programs.
在印度,宫颈癌是女性中第三大常见癌症。本研究旨在确定在印度迈索尔农村社区为基础的宫颈癌筛查项目中,联合使用 Gynocular 分诊诊断(Gynocular T2D/GT2D)和醋酸视觉检查(VIA)的可行性。
2015 年 11 月至 2016 年 8 月,印度公共卫生研究所(PHRII)在迈索尔区使用 VIA 和 GT2D 实施了一项移动宫颈癌筛查。女性接受阴道镜检查,VIA 阳性病例被识别。使用 GT2D 评估瑞典评分,评分>4 表示进一步监测或转诊治疗。为选定病例进行巴氏涂片检查。使用卡方检验和 Fisher 精确检验进行统计分析。
在登记的 199 名妇女中,有 176 名妇女纳入最终分析。23 名因阴道出血而被排除。妇女的平均年龄为 39 岁(范围 27-59 岁)。在 176 例中,38 例(21.6%)为 VIA 阳性,138 例(78.4%)为 VIA 阴性。在 6 例 VIA 阳性和 7 例 VIA 阴性妇女中观察到瑞典评分>4。2 例 VIA 阴性评分>4 的病例建议活检。
Gynocular 分诊避免了对 32 名(18.1%)参与者的过度治疗,并在 VIA 阴性病例中发现了 7 名瑞典评分>4 的受试者,如果仅使用 VIA,这些受试者将被忽略。总之,我们的研究表明,Gynocular 分诊在社区宫颈癌筛查项目中是可行的。