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首页> 外文期刊>Journal of Clinical Microbiology >Comparison of the Syva MicroTrak enzyme immunoassay and Gen-Probe PACE 2 with cell culture for diagnosis of cervical Chlamydia trachomatis infection in a high-prevalence female population.
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Comparison of the Syva MicroTrak enzyme immunoassay and Gen-Probe PACE 2 with cell culture for diagnosis of cervical Chlamydia trachomatis infection in a high-prevalence female population.

机译:Syva MicroTrak酶免疫测定法和Gen-Probe PACE 2与细胞培养法的比较,用于诊断高流行女性人群中的沙眼衣原体感染。

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摘要

Culture is currently considered the "gold standard" for detecting Chlamydia trachomatis infections. We evaluated the Syva MicroTrak enzyme immunoassay (EIA) and Gen-Probe PACE 2 tests, which detect chlamydial antigens and rRNA, respectively. These assays were compared with each other and with culture for the detection of C. trachomatis in cervical specimens obtained from 217 women attending a clinic for sexually transmitted diseases. The prevalence of infection was 22.1% by culture. The sensitivity, specificity, and positive and negative predictive values were 79.2, 98.2, 92.6, and 94.3%, respectively, for EIA. For PACE 2, the respective values were 77.1, 97.6, 90.1, and 93.7%. After corrections for two false-negative cultures, the sensitivities and specificities were 80 and 99.4%, respectively, for the EIA and 78 and 98.8%, respectively, for the probe assay. Quantitative evaluation of the results showed that false-negative results with either assay were associated with cultures that had low inclusion counts or were negative without subpassage. Analysis of nonculture results revealed that 2.3% of the EIA results and 4.6% of the probe assay results were within +/- 30% of the respective assay cutoff values. These included four false-negative (one EIA and three probe) and two false-positive (one EIA and one probe) results. The Syva MicroTrak EIA and the Gen-Probe PACE 2 assay are comparable to but significantly less sensitive than culture. Use of a grey zone may help identify the need for repeat or confirmatory testing.
机译:目前,培养被认为是检测沙眼衣原体感染的“黄金标准”。我们评估了Syva MicroTrak酶免疫分析(EIA)和Gen-Probe PACE 2测试,它们分别检测衣原体抗原和rRNA。将这些测定法相互比较,并与培养物进行了比较,以检测从参加性传播疾病诊所的217名妇女获得的宫颈样本中的沙眼衣原体。通过培养,感染的发生率为22.1%。对EIA的敏感性,特异性以及阳性和阴性预测值分别为79.2%,98.2、92.6和94.3%。对于PACE 2,相应的值为77.1、97.6、90.1和93.7%。校正两种假阴性培养物后,EIA的敏感性和特异性分别为80%和99.4%,探针分析的敏感性和特异性分别为78%和98.8%。对结果的定量评估表明,两种测定方法的假阴性结果均与包含物计数低或未传代的阴性培养物有关。非培养结果的分析表明,EIA结果的2.3%和探针测定结果的4.6%在各自测定的临界值的+/- 30%之内。这些结果包括四个假阴性(一个EIA和三个探针)和两个假阳性(一个EIA和一个探针)结果。 Syva MicroTrak EIA和Gen-Probe PACE 2分析法可与培养物媲美,但灵敏度明显低于培养物。使用灰色区域可能有助于确定是否需要重复或验证性测试。

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