首页> 外文期刊>Diagnostic microbiology and infectious disease >Diagnosis of Chlamydia trachomatis and Neisseria gonorrhoeae. Genitourinary infections in males by the Amplicor PCR assay of urine.
【24h】

Diagnosis of Chlamydia trachomatis and Neisseria gonorrhoeae. Genitourinary infections in males by the Amplicor PCR assay of urine.

机译:沙眼衣原体和淋病奈瑟菌的诊断。通过Amplicor PCR尿液检测男性的泌尿生殖系统感染。

获取原文
获取原文并翻译 | 示例
           

摘要

The Amplicor CT/NG polymerase chain reaction (PCR) test on urine specimens from males was prospectively evaluated against established specimens and laboratory methods for diagnosing Chlamydia trachomatis and Neisseria gonorrhoeae genitourinary infections, in patients from a remote region of Western Australia. Seventy-three males who were tested for both C. trachomatis and N. gonorrhoeae by both conventional methodology and Amplicor PCR on urine were enrolled in the study. Established testing comprised enzyme immunoassay/immunofluorescence antigen testing (EIA/IF) for C. trachomatis and microscopy and/or culture for N. gonorrhoeae on urethral swabs. Positive test results were confirmed using a set of criteria that included supplemental PCR testing and clinical history. Overall, 13.7% of patients were resolved as positive for C. trachomatis and 52.1% as positive for N. gonorrhoeae. The sensitivity and specificity of the Amplicor CT/NG PCR on male urine specimens for C. trachomatis were 80.0% (8/10) and 95.2% (60/63), compared with 60.0% (6/10) and 100.0% (63/63) for EIA/IF on urethral swabs. For N. gonorrhoeae, the sensitivity and specificity of the Amplicor CT/NG PCR on male urine specimens were both 100% (38/38 and 35/35, respectively) compared with 86.8% (33/38) and 100% (35/35) for microscopy and/or culture on urethral swabs. The results of this study indicate that the Amplicor CT/NG multiplex PCR test for C. trachomatis and N. gonorrhoeae performed on urine in males provides a highly sensitive, specific, and robust method for the diagnosis of both C. trachomatis and N. gonorrhoeae, for the early detection of both symptomatic and asymptomatic infected individuals.
机译:前瞻性地评估了来自男性尿液样本的Amplicor CT / NG聚合酶链反应(PCR)测试是否与已建立的样本和实验室方法相结合,以用于诊断西澳大利亚州偏远地区患者的沙眼衣原体和淋病奈瑟氏球菌泌尿生殖道感染。该研究纳入了73名通过常规方法和Amplicor PCR对沙眼衣原体和淋病奈瑟氏球菌进行检测的男性。已建立的测试包括沙眼衣原体的酶免疫测定/免疫荧光抗原测试(EIA / IF)和尿道拭子上的淋病奈瑟氏球菌的显微镜检查和/或培养。使用包括补充PCR测试和临床病史在内的一系列标准,确认阳性测试结果。总体而言,有13.7%的患者沙眼衣原体呈阳性,而淋病奈瑟菌呈阳性的占52.1%。 Amplicor CT / NG PCR对沙眼衣原体男性尿液标本的敏感性和特异性分别为80.0%(8/10)和95.2%(60/63),而60.0%(6/10)和100.0%(63) / 63)进行尿道拭子的EIA / IF检查。对于淋病奈瑟菌,Amplicor CT / NG PCR对男性尿液标本的敏感性和特异性均为100%(分别为38/38和35/35),而分别为86.8%(33/38)和100%(35 / 35)用于在尿道拭子上进行显微镜检查和/或培养。这项研究的结果表明,对男性尿液中的沙眼衣原体和淋病奈瑟氏菌进行Amplicor CT / NG多重PCR检测,为诊断沙眼衣原体和淋病奈瑟氏菌提供了高度灵敏,特异性强的方法,用于及早发现有症状和无症状感染的个体。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号