Beebe J L, Sharpton T R, Zanto S N, Steece R S, Rogers C, Mottice S L
Laboratory Division, Colorado Department of Public Health and Environment, Denver 80217, USA.
J Clin Microbiol. 1997 Feb;35(2):477-8. doi: 10.1128/jcm.35.2.477-478.1997.
The performance characteristics of the Gen-Probe Probe Competition Assay (PCA) used in conjunction with the Gen-Probe PACE 2 and 2C direct detection assays for Chlamydia trachomatis were examined. Data collected by five public health laboratories by using the Gen-Probe PACE 2 were pooled and analyzed. Of 25,081 endocervical and male urethral specimens tested by the PACE 2 assay, 773 were tested by PCA. Of 334 specimens initially positive by the PACE 2 assay with an initial PACE 2 result of greater than 2,000 relative light units (RLU), 333 (99.7%) were positive by PCA while 242 of 339 (71.4%) specimens with an initial result between the cutoff and 2,000 RLU were positive by PCA, and 35 of 100 (35%) specimens with initial results between 200 RLU and the cutoff were positive by PCA. An additional 10,938 specimens were tested by the PACE 2C assay. Of these, positive PCA results were obtained for 187 of 188 (99.5%) specimens with initial results of greater than 2,000 RLU, 99 of 163 (60.7%) of specimens in the range of cutoff to 2,000 RLU, and 12 of 100 (12%) in the range of 200 RLU to the cutoff. These results indicate that specimens greater than 2,000 RLU do not require a supplemental test and that additional positive results can be obtained by testing specimens with an initial result below the cutoff.
对Gen-Probe探针竞争分析(PCA)与Gen-Probe PACE 2和2C沙眼衣原体直接检测分析联合使用时的性能特征进行了检测。收集了五个公共卫生实验室使用Gen-Probe PACE 2检测的数据并进行了分析。在通过PACE 2分析检测的25081份宫颈内膜和男性尿道标本中,有773份通过PCA进行了检测。在最初通过PACE 2分析呈阳性且初始PACE 2结果大于2000相对光单位(RLU)的334份标本中,333份(99.7%)通过PCA呈阳性,而在最初结果介于临界值和2000 RLU之间的339份标本中,有242份(71.4%)通过PCA呈阳性,在最初结果介于200 RLU和临界值之间的100份标本中,有35份(35%)通过PCA呈阳性。另外10938份标本通过PACE 2C分析进行了检测。其中,在最初结果大于2000 RLU的188份标本中,有187份(99.5%)通过PCA获得了阳性结果,在临界值至2000 RLU范围内的163份标本中有99份(60.7%),在200 RLU至临界值范围内的100份标本中有12份(12%)。这些结果表明,大于2000 RLU的标本不需要进行补充检测,并且通过检测初始结果低于临界值的标本可以获得更多阳性结果。