Bronken T P, Dyke J W, Andruszewski M H
J Fam Pract. 1985 Jan;20(1):43-8.
An evaluation of a solid-phase enzyme immunoassay (Gonozyme) for detection of gonococcal antigen in cervical swab specimens was undertaken in 504 asymptomatic women undergoing routine gynecologic examination. The immunoassay was positive in all seven women with culture-proven gonorrhea. Negative immunoassay results were obtained in 482 of the 497 women with negative cultures (97.0 percent specificity). The enzyme immunoassay's performance equals or exceeds that of other rapid alternative methods of diagnosing cervical gonorrhea such as Gram stain or limulus lysate assay. Its usefulness, however, is limited by less than 100 percent specificity, particularly in low-prevalence populations. More studies are needed to ascertain the performance of both this immunoassay and modified Thayer-Martin culture techniques in diagnosing cervical gonorrhea in low-prevalence populations.
对504名接受常规妇科检查的无症状女性的宫颈拭子标本进行了一项用于检测淋球菌抗原的固相酶免疫测定法(Gonozyme)评估。在所有7名经培养证实患有淋病的女性中,免疫测定呈阳性。在497名培养结果为阴性的女性中,有482名免疫测定结果为阴性(特异性为97.0%)。该酶免疫测定法的性能等同于或超过了其他诊断宫颈淋病的快速替代方法,如革兰氏染色或鲎试剂检测法。然而,其效用受到特异性不足100%的限制,尤其是在低发病率人群中。需要更多研究来确定这种免疫测定法和改良的Thayer-Martin培养技术在低发病率人群中诊断宫颈淋病的性能。