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首页> 外文期刊>Journal of clinical virology: The official publication of the Pan American Society for Clinical Virology >Evaluation of the virtues and pitfalls in an HIV screening algorithm based on two fourth generation assays – A step towards an improved national algorithm
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Evaluation of the virtues and pitfalls in an HIV screening algorithm based on two fourth generation assays – A step towards an improved national algorithm

机译:基于第四代测定的HIV筛查算法评价 - 一种改进国家算法的步骤

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BackgroundFourth-generation immunoassays used for HIV screening, simultaneously detect anti-HIV antibodies and HIV-1 P24 antigen, but are prone to false-positive results. Usually, they are followed by highly specific third-generation assay, able to differentiate between HIV-1/2 infections. In Israel, screening algorithm is based on consecutive testing by two fourth-generation assays and confirmation by a third-generation test. ObjectivesTo evaluate the performance of this algorithm. Study designArchitect HIV1/2 Combo (Combo) reactive results were tested by Vidas HIV Duo Ultra (VD). Confirmation was by INNO-LIA HIV 1/2 or Geenius assays. Five-year results were retrospectively analyzed. HIV true positives (TPs), acute infected (AI), false-positives (FPs) and HIV negatives, were as defined by the algorithm. Results501,338 individuals were screened, of which 956 were TPs, 64 AI and 30?F?Ps. Specificity was almost 100% and positive predictive value 97%. VD was negative in 94% of confirmed Combo false-reactive individuals. The Combo results in the first tested sample differed substantially between TPs, AI and FPs, enabling the determination of a cutoff value that distinguished 94% of TPs and AI from FPs. ConclusionsAn algorithm is suggested that will use a single sample collection. HIV negative diagnosis will be based on Combo unreactive or Combo reactive/VD negative results. HIV positive diagnosis will be based on Combo reactive/ VD positive results, given a Combo value above a designated cutoff. Below this cutoff samples will be tested by a molecular assay. Since HIV-2 rarely occurs in Israel, the use of a third-generation confirmation assay should be discussed.
机译:背景生成的免疫测定用于HIV筛选,同时检测抗HIV抗体和HIV-1P24抗原,但易于呈假阳性结果。通常,它们之后是高度特异性的第三代测定,能够区分HIV-1/2感染。在以色列中,筛选算法基于由第三代测试的连续测试和第三代测试的确认。 ObjectiveSto评估该算法的性能。研究设计设计建筑艾滋病毒HIV1 / 2组合(组合)反应结果由VIDAS HIV Duo Ultra(VD)测试。 inno-lia hiv 1/2或geenius测定的确认。回顾性分析了五年的结果。 HIV真阳性(TPS),急性感染(AI),假阳性(FPS)和HIV负面否定,如算法所定义。结果筛选了501,338个个体,其中956个是TPS,64 AI和30?F?PS。特异性近100%,阳性预测值为97%。在94%的确认组合错误反应性别中,VD是负面的。在第一个测试样品中产生的组合在TPS,AI和FPS之间不同,使得能够确定从FPS区分94%的TP和AI的截止值。结论建议使用单个样本收集。 HIV阴性诊断将基于组合不反应或组合反应/ VD负面结果。考虑到以上指定截止值,HIV阳性诊断将基于组合反应/ VD阳性结果。在该截止样品下方将通过分子测定来测试。由于HIV-2很少发生在以色列中,因此应讨论使用第三代确认试验。

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