Literature DB >> 2199483

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

J A Kellogg1, J W Seiple, C L Murray, J S Levisky.   

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.

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Year:  1990        PMID: 2199483      PMCID: PMC267886          DOI: 10.1128/jcm.28.6.1108-1113.1990

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  35 in total

1.  Cytopathologic detection of Chlamydia trachomatis in vaginopancervical (Fast) smears.

Authors:  P K Gupta; M S Shurbaji; L J Mintor; S V Ermatinger; J Myers; T C Quinn
Journal:  Diagn Cytopathol       Date:  1988       Impact factor: 1.582

2.  Cytobrush in collection of cervical specimens for detection of Chlamydia trachomatis.

Authors:  J Moncada; J Schachter; M Shipp; G Bolan; J Wilber
Journal:  J Clin Microbiol       Date:  1989-08       Impact factor: 5.948

3.  Chlamydial infection. Improved methods of collection of material for culture from the urogenital tract and rectum.

Authors:  E M Dunlop; J D Vaughan-Jackson; S Darougar
Journal:  Br J Vener Dis       Date:  1972-12

Review 4.  Detection of chlamydiae by isolation and direct examination.

Authors:  R T Evans; R M Woodland
Journal:  Br Med Bull       Date:  1983-04       Impact factor: 4.291

5.  Diagnosis of Chlamydia trachomatis genital infections by cell culture and two enzyme immunoassays detecting different chlamydial antigens.

Authors:  J Mahony; S Castriciano; J Sellors; I Stewart; I Cunningham; S Landis; W Seidelman; L Grant; C Devlin; M Chernesky
Journal:  J Clin Microbiol       Date:  1989-09       Impact factor: 5.948

6.  Cytologic findings in cervical chlamydial infection.

Authors:  J Paavonen; E Purola
Journal:  Med Biol       Date:  1980-06

7.  Sequential cervical specimens and the isolation of Chlamydia trachomatis: factors affecting detection.

Authors:  J A Embil; H J Thiébaux; F R Manuel; L H Pereira; S W MacDonald
Journal:  Sex Transm Dis       Date:  1983 Apr-Jun       Impact factor: 2.830

8.  Chlamydia trachomatis: important relationships to race, contraception, lower genital tract infection, and Papanicolaou smear.

Authors:  M A Shafer; A Beck; B Blain; P Dole; C E Irwin; R Sweet; J Schachter
Journal:  J Pediatr       Date:  1984-01       Impact factor: 4.406

9.  Efficacy of duplicate genital specimens and repeated testing for confirming positive results for chlamydiazyme detection of Chlamydia trachomatis antigen.

Authors:  J A Kellogg; J W Seiple; J S Levisky
Journal:  J Clin Microbiol       Date:  1989-06       Impact factor: 5.948

10.  Lack of specificity of Chlamydiazyme for detection of vaginal chlamydial infection in prepubertal girls.

Authors:  K Porder; N Sanchez; P M Roblin; M McHugh; M R Hammerschlag
Journal:  Pediatr Infect Dis J       Date:  1989-06       Impact factor: 2.129

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  16 in total

1.  Value of confirmation of Chlamydiazyme enzyme immunoassay results in the detection of Chlamydia trachomatis.

Authors:  H Hallander; P Jonsson; B Gästrin
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1992-06       Impact factor: 3.267

2.  Accuracy of two enzyme immunoassays and cell culture in the detection of Chlamydia trachomatis in low and high risk populations in Senegal.

Authors:  E Van Dyck; N Samb; A D Sarr; L Van de Velden; J Moran; S Mboup; I Ndoye; J L Lamboray; A Meheus; P Piot
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1992-06       Impact factor: 3.267

3.  Effect of endocervical-specimen adequacy on detection of Chlamydia trachomatis by the APTIMA COMBO 2 assay.

Authors:  C K Rogers; B J Wood; P Rizzo; C A Gaydos
Journal:  J Clin Microbiol       Date:  2006-10-25       Impact factor: 5.948

4.  Use of flocked swabs and a universal transport medium to enhance molecular detection of Chlamydia trachomatis and Neisseria gonorrhoeae.

Authors:  Max Chernesky; Santina Castriciano; Dan Jang; Marek Smieja
Journal:  J Clin Microbiol       Date:  2006-03       Impact factor: 5.948

5.  Head-to-head evaluation of five chlamydia tests relative to a quality-assured culture standard.

Authors:  W J Newhall; R E Johnson; S DeLisle; D Fine; A Hadgu; B Matsuda; D Osmond; J Campbell; W E Stamm
Journal:  J Clin Microbiol       Date:  1999-03       Impact factor: 5.948

6.  An important proportion of genital samples submitted for Chlamydia trachomatis detection by PCR contain small amounts of cellular DNA as measured by beta-globin gene amplification.

Authors:  F Coutlée; M de Ladurantaye; C Tremblay; J Vincelette; L Labrecque; M Roger
Journal:  J Clin Microbiol       Date:  2000-07       Impact factor: 5.948

7.  Effect of endocervical specimen adequacy on ligase chain reaction detection of Chlamydia trachomatis.

Authors:  M J Loeffelholz; S J Jirsa; R K Teske; J N Woods
Journal:  J Clin Microbiol       Date:  2001-11       Impact factor: 5.948

8.  Diff-Quik stain as a simplified alternative to Papanicolaou stain for determination of quality of endocervical specimens submitted for PCR detection of Chlamydia trachomatis.

Authors:  J A Kellogg; J W Seiple; J L Klinedinst; E Stroll
Journal:  J Clin Microbiol       Date:  1996-10       Impact factor: 5.948

9.  Improved PCR detection of Chlamydia trachomatis by using an altered method of specimen transport and high-quality endocervical specimens.

Authors:  J A Kellogg; J W Seiple; J L Klinedinst; E S Stroll; S H Cavanaugh
Journal:  J Clin Microbiol       Date:  1995-10       Impact factor: 5.948

10.  Direct fluorescent-antibody confirmation of chlamydial antigen below the detection threshold of the chlamydiazyme enzyme-linked immunosorbent assay.

Authors:  J A Kellogg; J W Seiple; E S Stroll
Journal:  J Clin Microbiol       Date:  1993-06       Impact factor: 5.948

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