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4 个国家级人类免疫缺陷病毒行为监测系统点的丙型肝炎病毒抗体快速检测试剂的性能。

Performance of premarket rapid hepatitis C virus antibody assays in 4 national human immunodeficiency virus behavioral surveillance system sites.

机构信息

Division of Viral Hepatitis, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

出版信息

Clin Infect Dis. 2011 Oct;53(8):780-6. doi: 10.1093/cid/cir499.

Abstract

SUMMARY

Performance characteristics of rapid assays for hepatitis C virus antibody were evaluated in 4 National HIV Behavioral Surveillance System injection drug use sites. The highest assay-specific sensitivities achieved for the Chembio, MedMira and OraSure tests were 94.0%, 78.9%, and 97.4%, respectively; the highest specificities were 97.7%, 83.3%, and 100%, respectively.

BACKGROUND

The Centers for Disease Control and Prevention (CDC) estimates that 4.1 million Americans have been infected with hepatitis C virus (HCV) and 75%-80% of them are living with chronic HCV infection, many unaware of their infection. Persons who inject drugs (PWID) account for 57.5% of all persons with HCV antibody (anti-HCV) in the United States. Currently no point-of-care tests for HCV infection are approved for use in the United States.

METHODS

Surveys and testing for human immunodeficiency virus (HIV) and anti-HCV were conducted among persons who reported injection drug use in the past 12 months as part of the National HIV Behavioral Surveillance System in 2009. The sensitivity and specificity of point-of-care tests (finger-stick and 2 oral fluid rapid assays) from 3 manufacturers (Chembio, MedMira, and OraSure) were evaluated in field settings in 4 US cities.

RESULTS

Sensitivity (78.9%-97.4%) and specificity (80.0%-100.0%) were variable across assays and sites. The highest assay-specific sensitivities achieved for the Chembio, MedMira, and OraSure tests were 94.0%, 78.9% and 97.4%, respectively; the highest specificities were 97.7%, 83.3%, and 100%, respectively. In multivariate analysis, false-negative anti-HCV results were associated with HIV positivity for the Chembio oral assay (adjusted odds ratio, 8.4-9.1; P < .01) in 1 site (New York City).

CONCLUSIONS

Sensitive rapid anti-HCV assays are appropriate and feasible for high-prevalence, high-risk populations such as PWID, who can be reached through social service settings such as syringe exchange programs and methadone maintenance treatment programs.

摘要

摘要

在国家艾滋病行为监测系统的 4 个注射毒品使用点,评估了丙型肝炎病毒抗体快速检测的性能特征。 Chembio、MedMira 和 OraSure 检测的最高检测特异性敏感性分别为 94.0%、78.9%和 97.4%;最高特异性分别为 97.7%、83.3%和 100%。

背景

美国疾病控制与预防中心(CDC)估计,有 410 万美国人感染了丙型肝炎病毒(HCV),其中 75%-80%的人患有慢性 HCV 感染,许多人不知道自己的感染情况。在美国,注射毒品者(PWID)占所有 HCV 抗体(抗-HCV)感染者的 57.5%。目前,美国尚未批准任何用于 HCV 感染的即时检测。

方法

作为国家艾滋病行为监测系统的一部分,2009 年在过去 12 个月内报告注射吸毒的人群中进行了艾滋病毒(HIV)和抗-HCV 的调查和检测。在 4 个美国城市的现场环境中评估了来自 3 家制造商(Chembio、MedMira 和 OraSure)的即时检测(指尖和 2 种口腔液快速检测)的敏感性和特异性。

结果

不同检测方法和地点的敏感性(78.9%-97.4%)和特异性(80.0%-100.0%)各不相同。 Chembio、MedMira 和 OraSure 检测的最高检测特异性敏感性分别为 94.0%、78.9%和 97.4%;最高特异性分别为 97.7%、83.3%和 100%。在多变量分析中,在一个地点(纽约市),Chembio 口腔检测的假阴性抗-HCV 结果与 HIV 阳性相关(调整比值比,8.4-9.1;P<.01)。

结论

对于 PWID 等高危高流行人群,敏感的快速抗-HCV 检测是合适且可行的,他们可以通过诸如注射器交换计划和美沙酮维持治疗计划等社会服务场所来接触。

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