Shrier Lydia A, Dean Deborah, Klein Ellen, Harter Kimberly, Rice Peter A
Division of Adolescent/Young Adult Medicine, Children's Hospital Boston, Harvard Medical School, Boston, Mass, USA.
Am J Obstet Gynecol. 2004 Mar;190(3):654-62. doi: 10.1016/j.ajog.2003.09.063.
The purpose of this study was to examine the performance of different test types, specimen sources, and collection methods for screening of genital Chlamydia trachomatis infection in young women.
Asymptomatic women aged 16 to 25 years collected their own vaginal swabs and a first-voided urine specimen; a clinician collected urethral, vaginal, and endocervical swabs for culture and nucleic acid amplification tests, polymerase chain reaction and ligase chain reaction. A positive culture, 2 positive nucleic acid amplification tests, or 1 positive nucleic acid amplification test confirmed by a separate nested polymerase chain reaction comprised the criterion standard to define a C. trachomatis-infected woman.
The prevalence of C. trachomatis was 22% (30/139 women). All 9 test results were available for 126 participants (91%). Sensitivities were comparable for polymerase chain reaction and ligase chain reaction (52%-63%), except for urine polymerase chain reaction (44%), and were lower for culture (22%-37%); specificities were 99% to 100%, except for urine ligase chain reaction (91%). Positive predictive values were >93%, except for urine ligase chain reaction (65%); negative predictive values were 83% to 91%. Combining nucleic acid amplification test results from 2 different specimens improved sensitivities without compromising specificity.
When C. trachomatis infection was defined by multiple tests from different specimen sources, the sensitivity of any 1 test from a single specimen source was lower than generally reported. The limitations of the use of a single test to identify C. trachomatis infection should be considered when test type, specimen source, and collection method for screening young women is being determined.
本研究旨在探讨不同检测类型、标本来源及采集方法用于筛查年轻女性生殖道沙眼衣原体感染的性能。
16至25岁无症状女性自行采集阴道拭子和首次晨尿标本;临床医生采集尿道、阴道和宫颈拭子用于培养及核酸扩增检测,即聚合酶链反应和连接酶链反应。阳性培养结果、2次阳性核酸扩增检测结果或经单独巢式聚合酶链反应确认的1次阳性核酸扩增检测结果构成定义沙眼衣原体感染女性的标准。
沙眼衣原体感染率为22%(30/139名女性)。126名参与者(91%)的所有9项检测结果均可用。聚合酶链反应和连接酶链反应的敏感性相当(52%-63%),尿聚合酶链反应除外(44%),培养的敏感性较低(22%-37%);特异性为99%至100%,尿连接酶链反应除外(91%)。阳性预测值>93%,尿连接酶链反应除外(65%);阴性预测值为83%至91%。合并来自2种不同标本的核酸扩增检测结果可提高敏感性且不影响特异性。
当通过来自不同标本来源的多项检测来定义沙眼衣原体感染时,来自单一标本来源的任何1项检测的敏感性均低于一般报道。在确定筛查年轻女性的检测类型、标本来源及采集方法时,应考虑使用单一检测来识别沙眼衣原体感染的局限性。