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首页> 外文期刊>Journal of Clinical Microbiology >Detection of Chlamydia trachomatis and Neisseria gonorrhoeae by ligase chain reaction-based assays with clinical specimens from various sites: implications for diagnostic testing and screening.
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Detection of Chlamydia trachomatis and Neisseria gonorrhoeae by ligase chain reaction-based assays with clinical specimens from various sites: implications for diagnostic testing and screening.

机译:通过基于连接酶链反应的检测方法检测沙眼衣原体和淋病奈瑟氏球菌,并使用来自不同地点的临床标本:对诊断测试和筛查的意义。

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摘要

Ligase chain reaction (LCR)-based tests for the diagnosis of Chlamydia trachomatis and Neisseria gonorrhoeae infections in men and women attending a sexually transmitted disease clinic were evaluated. LCR testing of urethral swab and urine specimens from men and cervical swab and urine specimens from women was compared with culture of male urethral swabs and female cervical and urethral swabs, respectively. An expanded "gold standard" was defined as a positive culture or at least one specimen confirmed to be positive by LCR testing. The prevalence of C. trachomatis infection as detected by cell culture was 7.0% among 614 men and 5.0% among 602 women. By LCR, these values increased to 11.4 and 9.9% with urethral swabs and urine, respectively, for men and 9.6 and 9.1% with cervical swabs and urine, respectively, for women. Relative to the expanded gold standard, the sensitivity of cell culture with male urethral swabs or female cervical swabs was 57.3 and 45.5%, respectively, compared with corresponding values of 93.3 and 87.9% for LCR. The sensitivity of LCR with urine specimens was 77.3 and 78.8% for men and women, respectively. The prevalence of N. gonorrhoeae infection as detected by culture was 5.9% among 220 men and 2.9% among 383 women. The corresponding values were 8.2 and 5.5%, respectively, by LCR testing of swabs. Prevalence values by LCR testing of urine were 7.3% for men and 2.9% for women. The sensitivity of culture was 72.2% for men and 50.0% for women. The sensitivities of LCR were 100% with male urethral swabs, 95.4% with female cervical swabs, 88.9% with male urine, and 50.0% with female urine. These results indicate that the LCR-based assays represent a major improvement in C. trachomatis and N. gonorrhoeae diagnostics. The sensitivity of testing of urethral or cervical swabs by LCR was markedly greater than that by culture. The sensitivity of testing female or male urine specimens was equal to or greater than that of culturing cervical or urethral specimens. LCR testing of urine specimens may prove useful for screening for C. trachomatis.
机译:评估了基于连接酶链反应(LCR)的诊断方法,该方法可诊断出在性病门诊的男女沙眼衣原体和淋病奈瑟菌。分别比较了男性尿道拭子和女性宫颈拭子和女性尿道样本的LCR检测结果与男性尿道拭子以及女性宫颈和尿道拭子的培养情况。扩展的“金标准”定义为阳性培养物或至少一个通过LCR测试确认为阳性的标本。通过细胞培养检测到的沙眼衣原体感染的患病率在614名男性中为7.0%,在602名女性中为5.0%。通过LCR,男性尿道拭子和尿液的这些值分别增至11.4%和9.9%,女性宫颈癌拭子和尿液的这些值分别增至9.6%和9.1%。相对于扩展的金标准,使用男性尿道拭子或女性宫颈拭子进行细胞培养的敏感性分别为57.3和45.5%,而LCR的相应值分别为93.3和87.9%。男女对尿液中LCR的敏感性分别为77.3和78.8%。通过培养检测到的淋病奈瑟菌感染率在220名男性中为5.9%,在383名女性中为2.9%。通过棉签的LCR测试,相应的值分别为8.2%和5.5%。通过LCR检测尿液的患病率,男性为7.3%,女性为2.9%。男性的文化敏感性为72.2%,女性为50.0%。男性尿道拭子对LCR的敏感性为100%,女性宫颈拭子为95.4%,男性尿液为88.9%,女性尿液为50.0%。这些结果表明,基于LCR的检测方法代表了沙眼衣原体和淋病奈瑟氏菌诊断的重大改进。 LCR检测尿道或宫颈拭子的敏感性显着高于培养。测试女性或男性尿液样本的敏感性等于或大于培养宫颈或尿道样本的敏感性。尿液样本的LCR检测可能对筛查沙眼衣原体很有用。

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