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首页> 外文期刊>Journal of Clinical Microbiology >Performance of a nonisotopic DNA probe for detection of Chlamydia trachomatis in urogenital specimens.
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Performance of a nonisotopic DNA probe for detection of Chlamydia trachomatis in urogenital specimens.

机译:非同位素DNA探针在泌尿生殖道标本中检测沙眼衣原体的性能。

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The Gen-Probe PACE 2 assay (GP), a nonisotopic DNA probe, was evaluated by using cell culture as the method of reference. Specimens were collected from 260 men and 482 women visiting the outpatient department for sexually transmitted diseases at the University Hospital in Rotterdam, The Netherlands. The prevalences of Chlamydia culture-positive men and women were 13.2 and 8.6%, respectively. Sensitivity values for the male and female patients were 70.6 and 92.7%, respectively. Specificity values for these groups were 98.2 and 97.7%, respectively. Sensitivity was significantly lower when the number of inclusions in cell culture was low. Samples which showed a discordance between cell culture and GP results were retested by the polymerase chain reaction. If the results of the polymerase chain reaction were considered as the points of reference, the sensitivity and specificity of both GP and cell culture could be calculated. The performance of GP for females was comparable to that of cell culture. In males, the sensitivity of GP was considerably lower than that of cell culture (77.2 versus 91.4%), while specificity was somewhat higher (99.6 versus 99.1%). Compared with cell culture, the GP is a relatively simple and rapid test that is suitable for diagnosing Chlamydia infections in urogenital specimens.
机译:通过使用细胞培养作为参考方法评估了Gen-Probe PACE 2分析(GP)(一种非同位素的DNA探针)。从荷兰鹿特丹大学医院就诊的性传播疾病门诊部的260名男性和482名女性中收集了标本。衣原体培养阳性的男性和女性的患病率分别为13.2和8.6%。男性和女性患者的敏感度值分别为70.6和92.7%。这些组的特异性值分别为98.2和97.7%。当细胞培养物中的夹杂物数量少时,敏感性显着降低。通过聚合酶链反应重新测试显示细胞培养与GP结果不一致的样品。如果将聚合酶链反应的结果作为参考,则可以计算GP和细胞培养的敏感性和特异性。 GP对雌性的表现与细胞培养相当。在男性中,GP的敏感性显着低于细胞培养的敏感性(77.2对91.4%),而特异性则更高(99.6对99.1%)。与细胞培养相比,GP是一种相对简单,快速的检测方法,适用于诊断泌尿生殖道标本中的衣原体感染。

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