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男性沙眼衣原体检测。针对敏感尿道的敏感检测方法。

Detection of Chlamydia trachomatis in men. Sensitive tests for sensitive urethras.

作者信息

Hay P E, Thomas B J, McKenzie P, Taylor-Robinson D

机构信息

Division of Sexually Transmitted Diseases, Clinical Research Centre, Harrow, Middlesex, United Kingdom.

出版信息

Sex Transm Dis. 1993 Jan-Feb;20(1):1-4. doi: 10.1097/00007435-199301000-00001.

Abstract

The value of examining the centrifuged deposit from a first pass urine sample by an amplified enzyme-linked immunosorbent assay (ELISA) to detect Chlamydia trachomatis was assessed. The results were compared with those obtained by examining a urethral smear with a direct fluorescent antibody (DFA) test (MicroTrak; Syva, Palo Alto, CA). When the first pass urine sample yielded positive results for the IDEIA, but results of the DFA test of the corresponding urethral sample were negative, the remaining centrifuged deposit from the urine sample was examined by the DFA test. If results of this DFA test were positive, the IDEIA result was regarded as a true positive. Paired samples were collected by nursing staff from 190 men attending a clinic for sexually transmitted diseases (STDs). The quality of sampling thus reflected routine practice. The sensitivity of the IDEIA using first pass urine samples was 90% (37/41), and the sensitivity of the DFA test of urethral samples was 83% (34/41). The adoption of testing of first pass urine samples for the detection of C. trachomatis in STD clinics will not lead to a decrease in sensitivity for detecting C. trachomatis and will be more acceptable to patients than urethral swabbing.

摘要

评估了通过扩增酶联免疫吸附测定(ELISA)检测首次排尿尿液样本的离心沉淀物以检测沙眼衣原体的价值。将结果与通过直接荧光抗体(DFA)试验(MicroTrak;Syva,加利福尼亚州帕洛阿尔托)检查尿道涂片所获得的结果进行比较。当首次排尿尿液样本的IDEIA检测结果为阳性,但相应尿道样本的DFA试验结果为阴性时,对尿液样本剩余的离心沉淀物进行DFA试验检查。如果该DFA试验结果为阳性,则将IDEIA结果视为真阳性。护理人员从190名到性病诊所就诊的男性中收集配对样本。这样的采样质量反映了常规做法。使用首次排尿尿液样本的IDEIA的敏感性为90%(37/41),尿道样本DFA试验的敏感性为83%(34/41)。在性病诊所采用检测首次排尿尿液样本以检测沙眼衣原体不会导致检测沙眼衣原体的敏感性降低,并且比尿道拭子采样更易为患者接受。

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