首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Detection of Chlamydia trachomatis infections in women by Amplicor PCR: comparison of diagnostic performance with urine and cervical specimens.
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Detection of Chlamydia trachomatis infections in women by Amplicor PCR: comparison of diagnostic performance with urine and cervical specimens.

机译:通过Amplicor PCR检测女性沙眼衣原体感染:与尿液和宫颈标本的诊断性能比较。

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摘要

We used the Roche Amplicor PCR assay to compare urine and cervical swabs as sample material in the detection of Chlamydia trachomatis causing genital infections. The diagnostic performance of Amplicor PCR was compared with that of cell culture and the Gen-Probe PACE 2 assay with cervical specimens. If discrepant from other results, the specimens negative by PCR were diluted and reanalyzed to reveal PCR inhibitors. Of 666 patients, 39 (5.9%) were confirmed to have chlamydial infection. The respective sensitivity and specificity of Amplicor PCR were as follows: urine specimens, 82.0 and 99.7%; cervical specimens, 82.0 and 99.8%. Those for cell culture with cervical specimens were 84.6 and 100%. For the Gen-Probe PACE 2 assay, the sensitivity and specificity with cervical specimens were 79.5 and 100%, respectively. Without the effect of PCR inhibitors, the sensitivity of PCR with urine would have been 97.4%. Provided that the problems currently caused by inhibitors will be solved, the Amplicor PCR assay with urine specimens offers a tempting alternative for the diagnosis of C. trachomatis infection in women.
机译:我们使用罗氏Amplicor PCR分析法比较尿液和子宫颈拭子作为样本材料,以检测引起生殖器感染的沙眼衣原体。将Amplicor PCR的诊断性能与细胞培养和宫颈标本的Gen-Probe PACE 2测定进行了比较。如果与其他结果不一致,则将PCR阴性的样本稀释并重新分析以显示PCR抑制剂。在666名患者中,有39名(5.9%)被确认患有衣原体感染。 Amplicor PCR的各自灵敏度和特异性如下:尿液样本分别为82.0和99.7%;尿液样本分别为82.0和99.7%。宫颈标本分别为82.0和99.8%。用于宫颈标本细胞培养的细胞分别为84.6和100%。对于Gen-Probe PACE 2分析,对宫颈标本的敏感性和特异性分别为79.5和100%。如果没有PCR抑制剂的影响,尿液PCR的敏感性将达到97.4%。如果能够解决目前由抑制剂引起的问题,那么用尿液样本进行Amplicor PCR检测就可以为诊断女性沙眼衣原体感染提供诱人的选择。

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