首页> 外文期刊>Acta Cytologica: The Journal of Clinical Cytology and Cytopathology >Conventional Pap smear and liquid-based cytology as screening tools in low-resource settings in Latin America: experience of the Latin American screening study.
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Conventional Pap smear and liquid-based cytology as screening tools in low-resource settings in Latin America: experience of the Latin American screening study.

机译:常规子宫颈抹片涂片和基于液体的细胞学作为拉丁美洲资源贫乏地区的筛查工具:拉丁美洲筛查研究的经验。

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OBJECTIVE: To evaluate the performance of the conventional Pap test and liquid-based cytology (LBC) in an ongoing multicenter trial testing optional screening tools (cytology, screening colposcopy, visual inspection with acetic acid, visual inspection with Lugol's Iodine, cervicography and Hybrid Capture II [HCII] (Digene Brazil, Sao Paulo, Brazil) conventional and self-sampling), for cervical cancer in Brazil and Argentina. STUDY DESIGN: A cohort of 12,107 women attending four clinics (Campinas, Sao Paulo, Porto Alegre, Buenos Aires) were randomized into the 8 diagnostic arms. Women testing positive with any of the tests were referred for colposcopy, and cervical biopsies were used as the gold standard to assess performance characteristics of the diagnostic tests. Conventional Pap smears were sampled by all clinics (n = 10,240), and LBC (Autocyte PREP, [TriPath Imaging, Burlington, North Carolina, U.S.A.], n=320, and DNA-Citoliq [Digene Brazil], n =1,346) was performed by 1 of the clinics. RESULTS: Conventional Pap smears showed no squamous intraepithelial lesions (normal) in 8,946 (87.4%) and LBC in 1,373 (82.4%). Using high grade squamous intraepithelial lesions (HSIL) as the cutoff, Pap smears predicted high grade (cervical intraepithelial neoplasia [CIN] 3) with OR 63.0 (95% CI, 36.90-107.70), standard error (SE) 59%, SP 97.8%, positive predictive value (PPV) 68.1% and negative predictive value (NPV) 96.7%. The same figures for Autocyte PREP were: OR 9.0 (95% CI, 2.43-33.24), sensitivity (SE) 33.3%, specificity (SP) 100%, PPV 100% and negative PV (NPV) 88.8%. DNA-Citoliq detected CIN 3 as follows: OR 11.8 (95% CI 2.60-53.26), SE 40.0%, SP 94.6%, PPV 40.0% and NPV 94.6%. Lowering the cutoff to low grade squamous intraepithelial lesions increased SE and NPV but compromised SP and PPV. The detection rates for high grade lesions after an atypical squamous cells of undetermined significance diagnosis were similar with the 3 techniques. In our settings, the 3 methods of cervical cytology were slightly different in performance. The conventional Pap smear had the highest SE, while Autocyte PREP had 100% SP and PPV in detecting CIN3 with the HSIL cutoff. All 3 tests had lower SE but higher SP as compared to HCII.
机译:目的:在正在进行的多中心试验测试可选筛查工具(细胞学,筛查阴道镜检查,醋酸目视检查,Lugol碘液目视检查,宫颈造影和Hybrid Capture)中,评估常规巴氏试验和液基细胞学(LBC)的性能II [HCII](Digene Brazil,巴西圣保罗)常规和自采样),用于巴西和阿根廷的宫颈癌。研究设计:将在四个诊所(坎皮纳斯,圣保罗,阿雷格里港,布宜诺斯艾利斯)的12107名妇女队列随机分为8个诊断组。将任何一项测试呈阳性的妇女进行阴道镜检查,并将宫颈活检作为黄金标准以评估诊断测试的性能特征。所有诊所均对传统的子宫颈抹片检查进行了采样(n = 10,240),LBC(自噬细胞PREP,[TriPath Imaging,伯灵顿,北卡罗来纳州,美国],n = 320,DNA-Citoliq [Digene Brazil],n = 1,346)被采样。由其中一家诊所执行。结果:常规的子宫颈抹片涂片显示无鳞状上皮内病变(正常)的有8946例(87.4%),LBC的有1373例(82.4%)。使用高级别鳞状上皮内病变(HSIL)作为分界点,巴氏涂片检查可预测高级别(宫颈上皮内瘤样病变[CIN] 3)或为63.0(95%CI,36.90-107.70),标准误(SE)59%,SP 97.8 %,阳性预测值(PPV)68.1%和阴性预测值(NPV)96.7%。 Autocyte PREP的相同数字为:OR 9.0(95%CI,2.43-33.24),敏感性(SE)33.3%,特异性(SP)100%,PPV 100%和阴性PV(NPV)88.8%。 DNA-Citoliq检测到的CIN 3如下:或11.8(95%CI 2.60-53.26),SE 40.0%,SP 94.6%,PPV 40.0%和NPV 94.6%。将临界值降低至低级别鳞状上皮内病变会增加SE和NPV,但会损害SP和PPV。未明确诊断意义的非典型鳞状细胞后高级别病变的检出率与这三种技术相似。在我们的环境中,三种宫颈细胞学检查方法在性能上略有不同。传统的巴氏涂片检查具有最高的SE,而自噬细胞PREP在通过HSIL截止检测CIN3时具有100%的SP和PPV。与HCII相比,所有3个测试的SE都较低,但SP较高。

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