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宫颈管标本质量对沙眼衣原体检测及衣原体酶免疫法假阳性结果发生率的影响。

Effect of endocervical specimen quality on detection of Chlamydia trachomatis and on the incidence of false-positive results with the Chlamydiazyme method.

作者信息

Kellogg J A, Seiple J W, Murray C L, Levisky J S

机构信息

Pathology Department, York Hospital, Pennsylvania 17405.

出版信息

J Clin Microbiol. 1990 Jun;28(6):1108-13. doi: 10.1128/jcm.28.6.1108-1113.1990.

Abstract

Duplicate endocervical swabs were collected from 1,675 patients to assess the effects of variations in specimen quality on Chlamydiazyme (Abbott Laboratories) detection of Chlamydia trachomatis and the incidence of false-positive results. One swab (at random) from each patient was tested for C. trachomatis antigen by using the standard Chlamydiazyme procedure. A 200-microliter volume of 0.9% saline was added to the other swab from each patient. After vortexing, 20 microliters was smeared on a slide for Papanicolaou (Pap) staining and the remaining specimen was then tested with the Chlamydiazyme assay. The Chlamydiazyme result was positive for 170 (10.1%) and 165 (9.8%) of the stained and unstained duplicate specimens, respectively (no significant difference). Pap stains on smears from 1,536 (91.7%) of the patients were analyzed, and endocervical and/or metaplastic (E-M) cells were detected in 789 (51.4%) smears. Of these 1,536 stained and analyzed specimens, 150 (9.8%) were Chlamydiazyme positive but only 132 (88.0%) of the positive results were confirmed by repeating the test and using a monoclonal blocking antibody (Abbott). Confirmed Chlamydiazyme-positive results were obtained from only 34 (4.6%) of 747 specimens lacking E-M cells but from 98 (12.4%) of 789 specimens containing the cells (P less than 0.001). Of the 150 initially Chlamydiazyme-positive results obtained with Pap-stained, analyzed specimens, 12 (26.1%) of 46 were falsely positive from specimens lacking E-M cells but only 6 (5.8%) of 104 were falsely positive from specimens containing E-M cells (P less than 0.01). C. trachomatis antigen was detected significantly more frequently and false-positive results were significantly less common from specimens in which E-M cells were detected.

摘要

从1675例患者中采集两份宫颈拭子,以评估样本质量差异对衣原体酶检测法(雅培实验室)检测沙眼衣原体的影响以及假阳性结果的发生率。对每位患者的一份拭子(随机选取)采用标准的衣原体酶检测法检测沙眼衣原体抗原。向每位患者的另一份拭子中加入200微升0.9%的生理盐水。涡旋后,取20微升涂片进行巴氏染色,其余标本随后用衣原体酶检测法检测。染色和未染色的两份重复标本中,衣原体酶检测结果分别有170例(10.1%)和165例(9.8%)呈阳性(无显著差异)。对1536例(91.7%)患者的涂片进行巴氏染色分析,在789例(51.4%)涂片中检测到宫颈内膜和/或化生(E-M)细胞。在这1536份经染色并分析的标本中,150例(9.8%)衣原体酶检测呈阳性,但通过重复检测并使用单克隆阻断抗体(雅培),只有132例(88.0%)的阳性结果得到确认。在747份缺乏E-M细胞的标本中,只有34例(4.6%)得到确认的衣原体酶阳性结果,而在789份含有E-M细胞的标本中有98例(12.4%)得到确认(P<0.001)。在最初经巴氏染色并分析的标本中获得的150例衣原体酶阳性结果中,46份缺乏E-M细胞的标本中有12例(26.1%)为假阳性,而104份含有E-M细胞标本中只有6例(5.8%)为假阳性(P<0.01)。在检测到E-M细胞的标本中,沙眼衣原体抗原的检测频率显著更高,假阳性结果显著更少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22a2/267886/745c6b89a395/jcm00054-0044-a.jpg

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