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用于检测泌尿生殖系统衣原体感染的Amplicor沙眼衣原体检测法与细胞培养法的比较

Comparison of the Amplicor Chlamydia trachomatis test and cell culture for the detection of urogenital chlamydial infections.

作者信息

Catry M A, Borrego M J, Cardoso J, Azevedo J, Santo I

机构信息

Laboratório de Bacteriologia, Instituto Nacional de Saúde Dr. Ricardo Jorge, Lisboa, Portugal.

出版信息

Genitourin Med. 1995 Aug;71(4):247-50. doi: 10.1136/sti.71.4.247.

Abstract

OBJECTIVE

To compare the polymerase chain reaction (PCR) Amplicor Chlamydia trachomatis test with the cell culture method, in diagnosing urogenital chlamydial infections.

SUBJECTS

439 patients (327 women and 112 men) attending one STD clinic and Family Planning and Gynaecological Clinics in Lisbon, Portugal, between November 1993 and March 1994.

METHODS

In women, two endocervical swab samples were collected: one for PCR Amplicor and one for standard culture technique. Men were asked to submit 20 ml of urine (first pass urine) for PCR Amplicor and one urethral specimen was taken for culture. The order of collection of the specimens was rotated every 50 patients. Discrepant results were further analysed by a second PCR with primers directed against the C trachomatis major outer membrane protein (MOMP) and by direct fluorescent antibody (DFA).

RESULTS

After analysis of discrepancies, the adjusted sensitivity and specificity of PCR on endocervical specimens were 92.9% and 100% and the positive and negative predictive values were 100% and 99.7% respectively; on the urine samples these values were 100%, 99.1%, 100% and 99.1%, respectively.

CONCLUSION

These results indicate that the PCR Amplicor test is a rapid sensitive and specific assay for the detection of C trachomatis in urogenital infections and provides a non-invasive technique for screening chlamydia infection in men.

摘要

目的

比较聚合酶链反应(PCR)Amplicor沙眼衣原体检测法与细胞培养法在诊断泌尿生殖系统衣原体感染中的应用。

对象

1993年11月至1994年3月期间,在葡萄牙里斯本一家性传播疾病诊所以及计划生育和妇科诊所就诊的439例患者(327例女性和112例男性)。

方法

对于女性,采集两份宫颈拭子样本:一份用于PCR Amplicor检测,一份用于标准培养技术。男性需提交20毫升尿液(首次排尿)用于PCR Amplicor检测,并采集一份尿道标本用于培养。每50例患者轮换标本采集顺序。对结果不一致的情况,通过使用针对沙眼衣原体主要外膜蛋白(MOMP)的引物进行第二次PCR以及直接荧光抗体(DFA)检测进一步分析。

结果

在对差异进行分析后,宫颈标本PCR检测的校正灵敏度和特异性分别为92.9%和100%,阳性预测值和阴性预测值分别为100%和99.7%;尿液样本的这些值分别为100%、99.1%、100%和99.1%。

结论

这些结果表明,PCR Amplicor检测法是一种快速、灵敏且特异的检测泌尿生殖系统感染中沙眼衣原体的方法,为男性衣原体感染筛查提供了一种非侵入性技术。

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