Literature DB >> 1889175

Correlation of the percent of positive Chlamydia trachomatis direct fluorescent antibody detection tests with the adequacy of specimen collection.

C Howard1, D L Friedman, J K Leete, M L Christensen.   

Abstract

Chlamydia trachomatis is an obligate, intracellular parasite infecting the columnar and transitional cells lining the endocervix, uterus, fallopian tubes, rectum, urethra, and epididymis. We determined if the percent of specimens positive for C. trachomatis in the Microtrak Direct Specimen Test depended on the quality of specimens obtained. Female genital slides (649) were evaluated by the direct fluorescent antibody (DFA) test for the presence and numbers of (a) C. trachomatis elementary bodies and (b) columnar, transitional and squamous epithelial cells, and polymorphonuclear neutrophils (PMNs). Only 138 (21.3%) of the 649 slides were considered to be adequately taken, that is, containing columnar/transitional cells either alone or in conjunction with squamous cells and/or PMNs. Of the 138 adequate slides, 10 (7.2%) were C. trachomatis positive. However, 511 (78.7%) of the 649 slides were judged inadequate; 395 contained only squamous cells and/or PMNs, 19 were too thick to determine cell types, 46 contained only cell debris, and 51 contained neither cells nor debris. Only four (0.78%) of 511 were C. trachomatis positive. Thus adequate specimens containing columnar/transitional cells for C. trachomatis detection had a tenfold increase in the percent of positive results compared to inadequately collected specimens. By using the DFA test, one has the advantage of determining the adequacy of the specimens obtained as well as the presence of chlamydiae.

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Year:  1991        PMID: 1889175     DOI: 10.1016/0732-8893(91)90037-g

Source DB:  PubMed          Journal:  Diagn Microbiol Infect Dis        ISSN: 0732-8893            Impact factor:   2.803


  6 in total

1.  Rapid detection and typing of herpes simplex virus DNA in clinical specimens by the hybrid capture II signal amplification probe test.

Authors:  A P Cullen; C D Long; A T Lörincz
Journal:  J Clin Microbiol       Date:  1997-09       Impact factor: 5.948

2.  The value of non-culture techniques for diagnosis of Chlamydia trachomatis infections: making the best of a bad job.

Authors:  D Taylor-Robinson
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1992-06       Impact factor: 3.267

Review 3.  Current methods of laboratory diagnosis of Chlamydia trachomatis infections.

Authors:  C M Black
Journal:  Clin Microbiol Rev       Date:  1997-01       Impact factor: 26.132

4.  Comparison of cytobrushes with swabs for recovery of endocervical cells and for Chlamydiazyme detection of Chlamydia trachomatis.

Authors:  J A Kellogg; J W Seiple; J L Klinedinst; J S Levisky
Journal:  J Clin Microbiol       Date:  1992-11       Impact factor: 5.948

5.  Evaluation of the Biostar Chlamydia OIA assay with specimens from women attending a sexually transmitted disease clinic.

Authors:  M S Pate; P B Dixon; K Hardy; M Crosby; E W Hook
Journal:  J Clin Microbiol       Date:  1998-08       Impact factor: 5.948

Review 6.  A review of the human vs. porcine female genital tract and associated immune system in the perspective of using minipigs as a model of human genital Chlamydia infection.

Authors:  Emma Lorenzen; Frank Follmann; Gregers Jungersen; Jørgen S Agerholm
Journal:  Vet Res       Date:  2015-09-28       Impact factor: 3.683

  6 in total

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