Datta S Deblina, Koutsky Laura A, Ratelle Sylvie, Unger Elizabeth R, Shlay Judith, McClain Tracie, Weaver Beth, Kerndt Peter, Zenilman Jonathan, Hagensee Michael, Suhr Cristen J, Weinstock Hillard
Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.
Ann Intern Med. 2008 Apr 1;148(7):493-500. doi: 10.7326/0003-4819-148-7-200804010-00004.
Millions of women in the United States receive cervical screening in sexually transmitted disease (STD), family planning, and primary care clinical settings.
To inform current cervical screening programs.
Measurement of abnormal Papanicolaou (Pap) tests and high-risk human papillomavirus (HPV) infection among demographically diverse women who received routine cervical screening from January 2003 to December 2005 in the United States.
26 STD, family planning, and primary care clinics in 6 U.S. cities.
9657 women age 14 to 65 years receiving routine cervical screening.
Pap test results and high-risk HPV prevalence by Hybrid Capture 2 assay (Digene, Gaithersburg, Maryland).
Among 9657 patients, overall high-risk HPV prevalence by Hybrid Capture 2 testing was 23% (95% CI, 22% to 24%). Prevalence was highest among women age 14 to 19 years (35% [CI, 32% to 38%]) and lowest among women age 50 to 65 years (6% [CI, 4% to 8%]). Prevalence by clinic type (adjusted for age and city) ranged from 26% (CI, 24% to 29%) in STD clinics to 17% (CI, 16% to 20%) in primary care clinics. Women younger than 30 years of age whose Pap test showed atypical squamous cells of undetermined significance had a high-risk HPV prevalence of 53%; women 30 years of age or older with normal Pap tests had a 9% prevalence. Values did not vary substantially by clinic type.
Hybrid Capture 2 and Pap testing were noncentralized, and consent was required for enrollment.
High-risk HPV was widespread among women receiving cervical screening in the United States. Many women 30 years of age or older with normal Pap tests would need follow-up if Hybrid Capture 2 testing is added to cytology screening.
在美国,数百万女性在性传播疾病(STD)、计划生育及初级保健临床机构接受宫颈筛查。
为当前的宫颈筛查项目提供信息。
对2003年1月至2005年12月在美国接受常规宫颈筛查、人口统计学特征各异的女性进行巴氏涂片检查异常及高危人乳头瘤病毒(HPV)感染情况的测定。
美国6个城市的26家性传播疾病、计划生育及初级保健诊所。
9657名年龄在14至65岁之间接受常规宫颈筛查的女性。
采用杂交捕获2代检测法(Digene公司,马里兰州盖瑟斯堡)检测巴氏涂片检查结果及高危HPV感染率。
在9657名患者中,通过杂交捕获2代检测法得出的总体高危HPV感染率为23%(95%可信区间,22%至24%)。14至19岁女性的感染率最高(35%[可信区间,32%至38%]),50至65岁女性的感染率最低(6%[可信区间,4%至8%])。按诊所类型(校正年龄和城市因素)计算,性传播疾病诊所的感染率为26%(可信区间,24%至29%),初级保健诊所为17%(可信区间,16%至20%)。巴氏涂片检查显示意义不明确的非典型鳞状细胞的30岁以下女性,高危HPV感染率为53%;巴氏涂片检查正常的30岁及以上女性,感染率为9%。不同诊所类型的数值差异不大。
杂交捕获2代检测法和巴氏涂片检查未集中进行,入组需要获得同意。
在美国接受宫颈筛查的女性中,高危HPV感染很普遍。如果在细胞学筛查中增加杂交捕获2代检测法,许多巴氏涂片检查正常的30岁及以上女性将需要进行随访。