Implementation of visual inspection with acetic acid and Lugol's iodine for cervical cancer screening in rural China

被引:3
|
作者
Hu, Shang-Ying [1 ]
Zhao, Xue-Lian [1 ]
Zhao, Fang-Hui [1 ]
Wei, Li-Hui [2 ]
Zhou, Qi [3 ]
Niyazi, Mayinuer [4 ]
Liu, Ji-Hong [5 ]
Wang, Chun-Yan [6 ]
Li, Long-Yu [7 ]
Cheng, Xiao-Dong [8 ]
Duan, Xian-Zhi [9 ]
Sauvaget, Catherine [10 ]
Qiao, You-Lin [1 ]
Sankaranarayanan, Rengaswamy [11 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Natl Canc Ctr, Natl Clin Res Ctr Canc, Canc Hosp, Beijing, Peoples R China
[2] Peking Univ, Peoples Hosp, Beijing, Peoples R China
[3] Chongqing Univ, Canc Hosp, Chongqing, Peoples R China
[4] Peoples Hosp Xinjiang Uygur Autonomous Reg, Urumqi, Xinjiang, Peoples R China
[5] Sun Yat Sen Univ, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Canc Ctr, Guangzhou, Guangdong, Peoples R China
[6] Liaoning Canc Hosp & Inst, Shenyang, Liaoning, Peoples R China
[7] Jiangxi Maternal & Child Hlth Hosp, Nanchang, Jiangxi, Peoples R China
[8] Zhejiang Univ, Womens Hosp, Sch Med, Hangzhou, Zhejiang, Peoples R China
[9] Beijing Tongren Hosp, Beijing, Peoples R China
[10] Int Agcy Res Canc, Early Detect Prevent & Infect Branch, Lyon, France
[11] Int India, Res Triangle Inst, New Delhi, India
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
acetic acid; cervical cancer; Lugol's iodine; screening; visual inspection; POOLED ANALYSIS; ACCURACY; UGANDA; TESTS;
D O I
10.1002/ijgo.14368
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective To address the value of visual inspection where HPV-based screening is not yet available, we evaluated the real-world effectiveness of visual inspection with acetic acid (VIA) and with Lugol's iodine (VILI) as a primary screening method for cervical cancer in rural China. Methods A total of 206 133 women aged 30-59 years received two rounds of VIA/VILI screening for cervical cancer in 2006-2010. Women with positive screening results underwent colposcopy and direct biopsy, and were treated if cervical intraepithelial neoplasia grade 2 or worse (CIN2+) was diagnosed. Clinical effectiveness of VIA/VILI was evaluated by process and outcome measures. Results The VIA/VILI positivity rate, biopsy rate and detection rate of CIN2+ in the second round were significantly lower than in the first round. The 2-year cumulative detection rate of CIN2+ varied from 0.53% to 0.90% among the four cohorts initiated in 2006, 2007, 2008, and 2009. The first round of screening detected 60%-83% of CIN2, 70%-86% of CIN3, and 88%-100% of cervical cancer. Over 92% of CIN2+ were found at the early stage. Conclusion Multiple rounds of visual inspection with continuous training and quality assurance could act as a temporary substitutional screening method for cervical cancer in resource-restricted settings.
引用
收藏
页码:571 / 578
页数:8
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