Steingrímsson O, Jónsdóttir K, Olafsson J H, Karlsson S M, Pálsdóttir R, Davídsson S
Department of Microbiology, University of Iceland, Reykjavik, Iceland.
Sex Transm Dis. 1998 Jan;25(1):44-8. doi: 10.1097/00007435-199801000-00009.
To evaluate two automated amplification systems for the detection of Chlamydia trachomatis in urogenital specimens, the Cobas Amplicor (Roche Diagnostic Systems, Branchburg, NJ) and the LCx (Abbott Laboratories, Abbott Park, IL).
The two systems were compared testing specimens from 302 high-risk patients, including 98 female cervical swab specimens and 204 male urine specimens. The patients attended the state STD clinic in Reykjavik, Iceland, either because of symptoms or as a result of contract tracing.
The prevalence of C. trachomatis infection was 15.3% in women and 13.2% in men. For the male urine specimens, the sensitivity and specificity were 100% and 99.4% for the Cobas Amplicor and 74.1% and 100% for the LCx. In the cervical swabs, both systems detected all 15 true-positive specimens. The internal control used with the Cobas Amplicor detected inhibition in 2% of the male urine and 20% female cervical swabs, respectively.
The Cobas Amplicor demonstrated slightly better sensitivity than LCx in male urine specimens. Both systems offer the benefits of automation for routine diagnostic testing.
评估两种用于检测泌尿生殖系统标本中沙眼衣原体的自动化扩增系统,即Cobas Amplicor(罗氏诊断系统公司,新泽西州布兰奇堡)和LCx(雅培实验室,伊利诺伊州雅培公园)。
对来自302名高危患者的标本进行检测以比较这两种系统,其中包括98份女性宫颈拭子标本和204份男性尿液标本。这些患者因出现症状或作为接触者追踪的结果而前往冰岛雷克雅未克的国家性传播疾病诊所就诊。
女性沙眼衣原体感染率为15.3%,男性为13.2%。对于男性尿液标本,Cobas Amplicor的敏感性和特异性分别为100%和99.4%,LCx的敏感性和特异性分别为74.1%和100%。在宫颈拭子中,两种系统均检测出所有15份真阳性标本。与Cobas Amplicor一起使用的内部对照分别在2%的男性尿液和20%的女性宫颈拭子中检测到抑制作用。
在男性尿液标本中,Cobas Amplicor的敏感性略高于LCx。两种系统都为常规诊断检测提供了自动化的优势。