Suppr超能文献

采用酶联免疫吸附测定法检测女性沙眼衣原体时,首次晨尿标本与宫颈拭子标本的比较

Comparison of first-voided urine specimens with endocervical swab specimens for enzyme-linked immunosorbent assay detection of Chlamydia trachomatis in women.

作者信息

Kellogg J A, Vanderhoff B T, Seiple J W, Hick M E

机构信息

Pathology Department, York Hospital, Pa.

出版信息

Arch Fam Med. 1994 Aug;3(8):672-5. doi: 10.1001/archfami.3.8.672.

Abstract

OBJECTIVE

To compare first-voided urine specimens with paired endocervical swab specimens from women to determine the role of urine in complementing or replacing swab specimens for the detection of the chlamydial antigen.

DESIGN

For 18 months, both endocervical swab specimens (the criterion standard) and urine specimens were tested for the chlamydial antigen, using an enzyme-linked immunosorbent assay (Chlamydiazyme, Abbott Laboratories, North Chicago, Ill). Positive results were confirmed using a blocking reagent (Abbott Laboratories) and/or a direct fluorescent antibody test (Micro-Trak, Syva, Palo Alto, Calif). A low level of chlamydial antigen (below the enzyme-linked immunosorbent assay threshold recommended by the manufacturer) was also looked for and, when found, was confirmed by the direct fluorescent antibody test.

SETTING

Prenatal and family practice clinics in a 500-bed community hospital.

PATIENTS

Specimens were collected from 489 random asymptomatic or symptomatic women.

MAIN OUTCOME MEASURE

The detection of the chlamydial antigen from endocervical swab specimens was compared with the detection from first-voided urine specimens.

RESULTS

Acceptable swab and urine specimens were obtained from 300 (61.3%) of the patients. The antigen of Chlamydia trachomatis was confirmed in 20 (6.7%) of the 300 women. Of the infected patients, the antigen was detected in both swab and urine specimens for nine patients (45%), only in the swab specimens for eight (40%), and only in the urine specimens for three (15%). Testing urine in addition to endocervical swab specimens allowed for the detection of 18% more chlamydial infections, whereas confirming the presence of the antigen below the enzyme-linked immunosorbent assay cutoff resulted in the detection of 54% more infections.

CONCLUSIONS

Collecting multiple specimens and testing for low levels of chlamydial antigen may significantly improve the detection of chlamydial infections in women. First-voided urine may be an appropriate complementary specimen to endocervical swab specimens, but urine by itself does not allow for the adequate detection of the chlamydial antigen in women.

摘要

目的

比较女性首次晨尿标本与配对的宫颈拭子标本,以确定尿液在补充或替代拭子标本检测衣原体抗原方面的作用。

设计

在18个月的时间里,使用酶联免疫吸附试验(衣原体酶,雅培实验室,伊利诺伊州北芝加哥)对宫颈拭子标本(标准对照)和尿液标本进行衣原体抗原检测。阳性结果用阻断试剂(雅培实验室)和/或直接荧光抗体试验(Micro-Trak,赛瓦公司,加利福尼亚州帕洛阿尔托)进行确认。还对低水平的衣原体抗原(低于制造商推荐的酶联免疫吸附试验阈值)进行检测,一旦发现,用直接荧光抗体试验进行确认。

地点

一家拥有500张床位的社区医院的产前和家庭医疗诊所。

患者

从489名随机选取的无症状或有症状的女性中采集标本。

主要观察指标

比较宫颈拭子标本和首次晨尿标本中衣原体抗原的检测情况。

结果

300名(61.3%)患者获得了合格的拭子和尿液标本。300名女性中有20名(6.7%)确诊沙眼衣原体抗原阳性。在感染患者中,9名患者(45%)的拭子和尿液标本中均检测到抗原,8名(40%)仅在拭子标本中检测到,3名(15%)仅在尿液标本中检测到。除宫颈拭子标本外,检测尿液可使衣原体感染的检测率提高18%,而确认低于酶联免疫吸附试验临界值的抗原存在可使感染检测率提高54%。

结论

采集多个标本并检测低水平的衣原体抗原可能会显著提高女性衣原体感染的检测率。首次晨尿可能是宫颈拭子标本的合适补充标本,但仅靠尿液不能充分检测女性体内的衣原体抗原。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验