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首页> 外文期刊>Journal of Clinical Microbiology >Detection of Chlamydia trachomatis and Neisseria gonorrhoeae by Strand Displacement Amplification and Relevance of the Amplification Control for Use with Vaginal Swab Specimens
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Detection of Chlamydia trachomatis and Neisseria gonorrhoeae by Strand Displacement Amplification and Relevance of the Amplification Control for Use with Vaginal Swab Specimens

机译:链位移置换法检测沙眼衣原体和淋病奈瑟菌及与阴道拭子样本一起使用的扩增对照的相关性

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Vaginal swab specimens may be preferable to cervical swab or urine specimens for the detection of Chlamydia trachomatis and Neisseria gonorrhoeae because of the ease of specimen collection and transport. The purpose of this study was to evaluate whether vaginal swab specimens are equivalent to cervical swab specimens for the detection of N. gonorrhoeae and C. trachomatis by the Becton Dickinson strand displacement amplification assay (SDA) with the BDProbeTec ET instrument and then to evaluate the use of the amplification control in a clinical research setting. In the first phase, vaginal and cervical swab specimens were obtained from 455 symptomatic women aged 18 to 40 attending primary health care and sexually transmitted disease clinics. Thirty-nine specimens (8.6%) had true-positive results for N. gonorrhoeae and 37 specimens (8.1%) had true-positive results for C. trachomatis. The sensitivity of SDA was superior to that of culture for the detection of N. gonorrhoeae with vaginal swab specimens and equivalent to that of the Roche PCR for the detection of C. trachomatis with cervical swab specimens. In the second phase of the study, 1,411 consecutively collected vaginal swab specimens were evaluated, with 357 (25.3%) specimens giving indeterminate readings on the basis of the result for the amplification control. The prevalences of sexually transmitted pathogens in vaginal swab specimens with and without use of the amplification control were 6.0 and 5.8%, respectively, for C. trachomatis and 3.1 and 3.0%, respectively, for N. gonorrhoeae. Although, vaginal swab specimens were equivalent to cervical swab specimens for the detection of N. gonorrhoeae and C. trachomatis by SDA with respect to sensitivity, one in four vaginal swab specimens yielded an indeterminate result when the amplification control was used. The amplification control has limited value for use with vaginal swab specimens.
机译:阴道拭子标本比宫颈拭子或尿液标本更适合于检测沙眼衣原体和淋病奈瑟菌,因为它们易于收集和运输。这项研究的目的是评估阴道拭子样本是否等同于宫颈拭子样本以检测 N。淋病菌 C。 BDProbeTec ET仪器通过Becton Dickinson链置换扩增分析(SDA)检测沙眼,然后评估该扩增对照在临床研究中的用途。在第一阶段,从455名有症状的18岁至40岁有症状的妇女那里获得了阴道和宫颈拭子样本,这些妇女在初级卫生保健和性病诊所就诊。 39个标本(8.6%)的N值为真。淋病菌和37个标本(8.1%)的 C均为真阳性。沙眼。 SDA的检测灵敏性优于培养物。淋球菌带有阴道拭子标本,与Roche PCR等同,用于检测 C。带有子宫颈拭子标本的沙眼。在研究的第二阶段,评估了1,411个连续采集的阴道拭子样本,根据扩增对照的结果,其中357个样本(25.3%)的读数不确定。对于 C,使用和不使用扩增对照的阴道拭子样本中性传播病原体的患病率分别为6.0%和5.8%。沙眼 N分别为3.1%和3.0%。 虽然,阴道拭子标本等同于宫颈拭子标本以检测 N。淋病菌 C。通过SDA检测沙眼的敏感性,在使用扩增对照时,四分之一的阴道拭子样本产生不确定的结果。扩增对照对阴道拭子标本的使用价值有限。

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