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对无症状女性进行沙眼衣原体的首次晨尿聚合酶链反应检测。

First-void urine testing for Chlamydia trachomatis by polymerase chain reaction in asymptomatic women.

作者信息

Paukku M, Puolakkainen M, Apter D, Hirvonen S, Paavonen J

机构信息

Department of Obstetrics and Gynecology, University of Helsinki, Finland.

出版信息

Sex Transm Dis. 1997 Jul;24(6):343-6. doi: 10.1097/00007435-199707000-00006.

Abstract

BACKGROUND

Because Chlamydia trachomatis infections are usually asymptomatic or minimally symptomatic, diagnosis is often delayed.

GOAL

To perform a comparative study of first-void urine (FVU) polymerase chain reaction (PCR) testing and endocervical swab antigen testing in the diagnosis of C. trachomatis infection among asymptomatic women.

STUDY DESIGN

The study population consisted of 1,090 unselected women attending a family planning clinic or a university student health clinic. Calculations of test performances were based on an expanded reference standard including enzyme immunoassay (EIA) or PCR tests confirmed by direct fluorescence antibody (DFA) test or major outer membrane protein PCR test, respectively.

RESULTS

The overall prevalence of C. trachomatis infection was 5.6%. After resolution of discrepant specimens, FVU PCR detected 85% (52/61) and endocervical swab EIA/DFA 90% (55/61) of confirmed positive cases.

CONCLUSIONS

These results indicate that the FVU PCR test is an accurate, noninvasive screening method and can replace endocervical swab EIA in the detection of C. trachomatis infection in low-prevalence populations.

摘要

背景

由于沙眼衣原体感染通常无症状或症状轻微,诊断往往会延迟。

目的

对首次晨尿(FVU)聚合酶链反应(PCR)检测和宫颈拭子抗原检测在无症状女性沙眼衣原体感染诊断中的应用进行比较研究。

研究设计

研究人群包括1090名未经过筛选的女性,她们来自一家计划生育诊所或一所大学的学生健康诊所。检测性能的计算基于一种扩展的参考标准,分别包括通过直接荧光抗体(DFA)检测或主要外膜蛋白PCR检测确认的酶免疫测定(EIA)或PCR检测。

结果

沙眼衣原体感染的总体患病率为5.6%。在解决了有差异的标本后,FVU PCR检测出85%(52/61)的确诊阳性病例,宫颈拭子EIA/DFA检测出90%(55/61)的确诊阳性病例。

结论

这些结果表明,FVU PCR检测是一种准确、无创的筛查方法,在低患病率人群中检测沙眼衣原体感染时可替代宫颈拭子EIA检测。

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