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异常细胞学检查后宫颈上皮内瘤变 3 级或更高级别病变的长期累积发生率:HIV 感染的影响。

Long-term cumulative incidence of cervical intraepithelial neoplasia grade 3 or worse after abnormal cytology: impact of HIV infection.

机构信息

Department of Obstetrics & Gynecology, Washington University School of Medicine, St. Louis, MO.

出版信息

Int J Cancer. 2014 Apr 15;134(8):1854-61. doi: 10.1002/ijc.28523. Epub 2013 Oct 29.

Abstract

To estimate the long term cumulative risk for cervical intraepithelial neoplasia grade 3 or worse after an abnormal cervical Pap test and to assess the effect of HIV infection on that risk. Participants in the Women's Interagency HIV Study were followed semiannually for up to 10 years. Pap tests were categorized according to the 1991 Bethesda system. Colposcopy was prescribed within 6 months of any abnormality. Risk for biopsy-confirmed CIN3 or worse after abnormal cytology and at least 12 months follow-up was assessed using Kaplan-Meier curves and compared using log-rank tests. Risk for CIN2 or worse was also assessed, since CIN2 is the threshold for treatment. After a median of 3 years of observation, 1,947 (85%) women subsequently presented for colposcopy (1,571 [81%] HIV seropositive, 376 [19%] seronegative). CIN2 or worse was found in 329 (21%) of HIV seropositive and 42 (11%) seronegative women. CIN3 or worse was found in 141 (9%) of seropositive and 22 (6%) seronegative women. In multivariable analysis, after controlling for cytology grade HIV seropositive women had an increased risk for CIN2 or worse (H.R. 1.66, 95% C.I 1.15, 2.45) but higher risk for CIN3 or worse did not reach significance (H.R. 1.33, 95% C.I. 0.79, 2.34). HIV seropositive women with abnormal Paps face a marginally increased and long-term risk for cervical disease compared to HIV seronegative women, but most women with ASCUS and LSIL Pap results do not develop CIN2 or worse despite years of observation.

摘要

为了评估异常宫颈巴氏涂片检查后的宫颈上皮内瘤变 3 级或更高级别(CIN3)的长期累积风险,并评估 HIV 感染对该风险的影响,本研究纳入了妇女卫生机构 HIV 研究(Women's Interagency HIV Study)的参与者,对其进行了长达 10 年的半年度随访。巴氏涂片检查结果按照 1991 年的拜尔系统(Bethesda system)进行分类。任何异常情况发生后 6 个月内进行阴道镜检查。使用 Kaplan-Meier 曲线评估异常细胞学和至少 12 个月随访后活检证实的 CIN3 或更高级别(CIN3)的风险,并使用对数秩检验进行比较。由于 CIN2 是治疗的阈值,因此也评估了 CIN2 或更高级别的风险。中位随访 3 年后,1947 名(85%)女性随后进行了阴道镜检查(1571 名[81%]HIV 血清阳性,376 名[19%]血清阴性)。329 名(21%)HIV 血清阳性和 42 名(11%)血清阴性女性发现 CIN2 或更高级别病变。141 名(9%)血清阳性和 22 名(6%)血清阴性女性发现 CIN3 或更高级别病变。多变量分析显示,在控制了细胞学分级后,HIV 血清阳性女性发生 CIN2 或更高级别病变的风险增加(HR 1.66,95%CI 1.15,2.45),但 CIN3 或更高级别病变的风险增加没有达到统计学意义(HR 1.33,95%CI 0.79,2.34)。与 HIV 血清阴性女性相比,HIV 血清阳性且巴氏涂片异常的女性面临着稍高的长期宫颈疾病风险,但大多数 ASCUS 和 LSIL 巴氏涂片结果的女性尽管经过多年观察,也不会发展为 CIN2 或更高级别病变。

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Incidence of cervical precancers among HIV-seropositive women.HIV 血清阳性女性中宫颈上皮内瘤变的发病率。
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