首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Comparison of three commercially available amplification assays AMP CT LCx and COBAS AMPLICOR for detection of Chlamydia trachomatis in first-void urine.
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Comparison of three commercially available amplification assays AMP CT LCx and COBAS AMPLICOR for detection of Chlamydia trachomatis in first-void urine.

机译:三种市售扩增检测AMP CTLCx和COBAS AMPLICOR的比较用于检测初次排尿的沙眼衣原体。

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摘要

We compared the Gen-Probe transcription-mediated amplification assay (AMP CT), the Abbott LCx assay, and the Roche COBAS AMPLICOR assay for the detection of Chlamydia trachomatis in a mixed population in urine samples. First-void urine, urethral specimens, and cervical specimens in females were obtained from 1,000 patients (544 males and 456 females) visiting the outpatient sexually transmitted disease clinic of our hospital. The prevalence of C. trachomatis infection was 7.7% as determined by tissue culture of urethral and cervical specimens. The sensitivities of LCx, COBAS AMPLICOR, and AMP CT compared to cell culture were 79, 86, and 78%, respectively. Sensitivity and specificity were recalculated by using a new "gold standard", i.e., a sample was considered to be true positive if two or more techniques yielded positive results. Specimens positive only by cell culture or positive in only one commercial amplification technique were retested by a previously described in-house PCR. After discordance analysis the sensitivities of LCx, COBAS AMPLICOR, and AMP CT were 84, 93, and 85%, respectively. Specificity exceeded 99% for all three assays. With each method the sensitivity was lower for urine samples from females compared to urine samples from males. By application of this new gold standard, existing differences between methods are highlighted; future evaluations of new techniques should be validated against two or more amplification assays.
机译:我们比较了Gen-Probe转录介导的扩增测定(AMP CT),Abbott LCx测定和Roche COBAS AMPLICOR测定在尿液样本中混合人群中沙眼衣原体的检测。从我院门诊性病门诊的1,000例患者(男544例,女456例)中获得女性的第一空尿,尿道标本和宫颈标本。根据尿道和宫颈标本的组织培养确定,沙眼衣原体感染的患病率为7.7%。与细胞培养相比,LCx,COBAS AMPLICOR和AMP CT的敏感性分别为79%,86%和78%。通过使用新的“金标准”重新计算敏感性和特异性,即,如果两种或更多种技术产生阳性结果,则样品被视为真实阳性。仅通过细胞培养呈阳性或仅在一种商业扩增技术中呈阳性的标本通过先前描述的内部PCR重新测试。经过不一致分析后,LCx,COBAS AMPLICOR和AMP CT的灵敏度分别为84%,93%和85%。所有三种测定的特异性均超过99%。每种方法对女性尿液样品的敏感性均低于男性尿液样品。通过应用这一新的金标准,突出了方法之间的现有差异。未来对新技术的评估应针对两个或多个扩增试验进行验证。

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