Clark A M, Steece R, Crouse K, Campbell J, Zanto S, Kartchner D, Mottice S, Pettit D
University of Washington, Seattle, Washington, USA.
Sex Transm Dis. 2001 Oct;28(10):565-8. doi: 10.1097/00007435-200110000-00002.
Ligase chain reaction (LCR), a nucleic acid amplification assay, is a highly specific and sensitive test for detecting Chlamydia trachomatis in cervical and urethral swabs as well as first-void urine specimens.
To examine the suitability of using the LCR test to detect C trachomatis in pooled cervical specimens.
The performance of LCR in pooled specimens was compared with individual specimen testing at six laboratories using 3,170 cervical swab specimens randomly selected from specimens received for routine testing in the participating laboratories. These samples then were combined consecutively into 634 pools of 5 specimens and 317 pools of 10 specimens. A reduced sample to cutoff ratio of 0.2 or more was used for the pooled specimens.
Of the 188 positive specimens (98.9%), 186 were identified when single specimens were analyzed. When pools of 5 or 10 specimens were evaluated, 99.5% and 98.9% of the positive swabs, respectively, were identified correctly. Two positive specimens were detected only through pooling.
Pooling samples for detection of C trachomatis by LCR is sensitive and specific. Depending on the prevalence of infection (positivity), LCR testing may result in cost savings, as compared with individual testing of specimens.
连接酶链反应(LCR)是一种核酸扩增检测方法,是检测宫颈和尿道拭子以及首次晨尿标本中沙眼衣原体的高度特异性和敏感性检测。
检验使用LCR检测法检测合并宫颈标本中沙眼衣原体的适用性。
在六个实验室中,将LCR在合并标本中的性能与单个标本检测进行比较,使用从参与实验室接收的常规检测标本中随机选择的3170份宫颈拭子标本。然后将这些样本连续合并为634个每组5份标本的样本池和317个每组10份标本的样本池。合并标本的样本与临界值之比降低至0.2或更低。
在188份阳性标本中(98.9%),单个标本分析时鉴定出186份。当评估每组5份或10份标本的样本池时,分别正确鉴定出99.5%和98.9%的阳性拭子。仅通过合并检测出两份阳性标本。
通过LCR合并样本检测沙眼衣原体具有敏感性和特异性。根据感染率(阳性率),与单个标本检测相比,LCR检测可能会节省成本。