摘要
目的:对C learV iew CT快速诊断试剂盒检测女性生殖道的沙眼衣原体进行方法学评价。方法:采集每名受试者宫颈分泌物拭子2份,将之随机分为2组,以荧光定量PCR为参比试验,评价C lear-V iew CT快速诊断试剂盒在女性生殖道沙眼衣原体感染的应用性能。结果:设置荧光定量PCR为参比试验,C learV iew快速诊断试剂盒检测女性生殖道衣原体的敏感性为32.73%,特异性为88.52%,约登指数为0.2125。在感染率为28.95%的性服务工作者人群中应用该试剂盒检测生殖道沙眼衣原体时,其验后概率为53.74%。结论:C learV iew CT快速试剂盒的特异性尚可,但其敏感性差;在感染率达28.95%的女性性服务工作者人群应用C learV iew快速试剂盒检测生殖道衣原体感染,检测阳性者来诊断衣原体感染的把握度为53.74%。
Objective: Evaluate clearview CT rapid test kit in testing for female genital tract chlamydia trachomatis infection. Methods :Two vaginal swabs from each participant were collected and samples were divided into two groups randomly, fluorescent quantitation PCR has been taken as a reference, clearview CT rapid test kit to be used in chlamydia trachomatis detected. Results: The clearview rapid test kit had a sensitivity of 32.73%, a specificity of 88.52% and a Youden index of 0. 2125. Female commercial sex worker (FCSW) population with an infection rate of 28.95%, and the posterior probability was 53.74%. Conclusion :The clearview CT rapid test kit showed adequate specificity and low sensitivity. FCSW with an infection rate of 28.95%, whom detected by clearview rapid test kit, was found a CT infection rate of 53.74%.
出处
《岭南皮肤性病科杂志》
2006年第4期282-284,290,共4页
Southern China Journal of Dermato-Venereology
关键词
沙眼衣原体
实验室诊断
方法学评价
Chlamydia trachomatis
Laboratory diagnosis
Evaluation