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A dual point-of-care test shows good performance in simultaneously detecting nontreponemal and treponemal antibodies in patients with syphilis: A multisite evaluation study in China

机译:双重即时检验显示出梅毒患者同时检测非梅毒和梅毒抗体的良好性能:一项在中国的多点评估研究

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Background. Rapid point-of-care (POC) syphilis tests based on simultaneous detection of treponemal and nontreponemal antibodies (dual POC tests) offer the opportunity to increase coverage of syphilis screening and treatment. This study aimed to conduct a multisite performance evaluation of a dual POC syphilis test in China.Methods. Participants were recruited from patients at sexually transmitted infection clinics and high-risk groups in outreach settings in 6 sites in China. Three kinds of specimens (whole blood [WB], fingerprick blood [FB], and blood plasma [BP]) were used for evaluating sensitivity and specificity of the Dual Path Platform (DPP) Syphilis Screen and Confirm test using its treponemal and nontreponemal lines to compare Treponema pallidum particle agglutination (TPPA) assay and toluidine red unheated serum test (TRUST) as reference standards.Results. A total of 3134 specimens (WB 1323, FB 488, and BP 1323) from 1323 individuals were collected. The sensitivities as compared with TPPA were 96.7% for WB, 96.4% for FB, and 94.6% for BP, and the specificities were 99.3%, 99.1%, and 99.6%, respectively. The sensitivities as compared with TRUST were 87.2% for WB, 85.8% for FB, and 88.4% for BP, and the specificities were 94.4%, 96.1%, and 95.0%, respectively. For specimens with a TRUST titer of 1:4 or higher, the sensitivities were 100.0% for WB, 97.8% for FB, and 99.6% for BP.Conclusions. DPP test shows good sensitivity and specificity in detecting treponemal and nontreponemal antibodies in 3 kinds of specimens. It is hoped that this assay can be considered as an alternative in the diagnosis of syphilis, particularly in resource-limited areas. ? 2012 The Author.
机译:背景。基于即时检测梅毒和非梅毒抗体的快速即时梅毒检测(双重POC检测)提供了增加梅毒筛查和治疗覆盖率的机会。本研究旨在对中国双重POC梅毒测试进行多站点性能评估。在中国6个地区的性传播感染诊所和高危人群中从患者中招募参与者。使用三种样本(全血[WB],指尖血[FB]和血浆[BP])评估双通道平台(DPP)梅毒筛查的敏感性和特异性,并使用其梅毒螺旋体和非梅毒螺旋体进行确认试验比较梅毒螺旋体颗粒凝集法(TPPA)和甲苯胺红未加热血清试验(TRUST)作为参考标准。总共收集了来自1323个个体的3134个样本(WB 1323,FB 488和BP 1323)。与TPPA相比,WB的敏感性为96.7%,FB的敏感性为96.4%,BP的敏感性为94.6%,特异性分别为99.3%,99.1%和99.6%。与TRUST相比,WB的敏感性为87.2%,FB的敏感性为85.8%,BP的敏感性为88.4%,特异度分别为94.4%,96.1%和95.0%。对于TRUST滴度为1:4或更高的样品,WB的灵敏度为100.0%,FB的灵敏度为97.8%,BP的灵敏度为99.6%。 DPP检测在检测3种标本中的血清和非血清蛋白抗体方面显示出良好的灵敏度和特异性。希望该测定法可以被认为是梅毒诊断的一种替代方法,特别是在资源有限的地区。 ? 2012作者。

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