Genç M, Stary A, Bergman S, Mårdh P A
Institute of Clinical Bacteriology, University of Uppsala, Sweden.
APMIS. 1991 May;99(5):455-9.
Cervical, urethral and first-void urine (FVU) specimens from 196 men and 245 women attending a venereal outpatient clinic were studied by culture and a commercial enzyme immunoassay (EIA) (CHLAMYDIAZYME). Confirmatory chlamydial testing by a direct fluorescence assay (DFA) (MICROTRAK) was performed on the sediments of the positive EIA samples from culture-negative patients. Chlamydia trachomatis was isolated from 11% of the men and 12% of the women. Of the women, 67% were positive in both sampling sites and 33% in the cervix only. No further cases were found when a female urethral swab was cultured. All the chlamydia-positive urine samples were obtained from women who were positive in the urethra. The denominator used to calculate sensitivities was the combination of patients with culture- and EIA-positive results which could be confirmed by DFA. The sensitivity of our culture method was 85% for men and 77% for women. In men, the sensitivity of EIA was greater on urine than on urethral specimens (77% vs 62%; p less than 0.1). In women, the sensitivity of EIA on urine was significantly poorer than that on cervical specimens (54% vs 85%, p less than 0.001). The specificity of EIA ranged between 94 and 100%. Our study suggests that it may be worth using FVU in a trial for the diagnosis of genital chlamydial infections in symptomatic men, but not in symptomatic women.
对196名男性和245名女性性病门诊患者的宫颈、尿道和首次晨尿(FVU)标本进行了培养和商业酶免疫测定(EIA)(衣原体酶检测)研究。对培养阴性患者的EIA阳性样本沉淀物进行直接荧光测定(DFA)(微迹检测)以进行衣原体确诊检测。沙眼衣原体从11%的男性和12%的女性中分离出来。在女性中,67%在两个采样部位均为阳性,仅宫颈阳性的占33%。培养女性尿道拭子未发现更多病例。所有衣原体阳性尿液样本均来自尿道阳性的女性。用于计算敏感性的分母是培养和EIA结果均为阳性且可通过DFA确认的患者组合。我们的培养方法对男性的敏感性为85%,对女性为77%。在男性中,EIA对尿液的敏感性高于尿道标本(77%对62%;p<0.1)。在女性中,EIA对尿液的敏感性明显低于宫颈标本(54%对85%,p<0.001)。EIA的特异性在94%至100%之间。我们的研究表明,对于有症状男性的生殖器衣原体感染诊断试验,使用FVU可能是值得的,但对有症状女性则不然。