Literature DB >> 7502188

Laboratory to laboratory variation in Chlamydia trachomatis culture practices.

M S Pate1, E W Hook.   

Abstract

GOAL OF THIS STUDY: To compare laboratory to laboratory variability in methods of cell culture for Chlamydia trachomatis performed by North American research laboratories. STUDY
DESIGN: The authors administered a standardized 54-question survey to laboratories that had published articles in any of three medical journals reporting on the use of cell culture to identify individuals with C. trachomatis infection. Laboratory to laboratory variability in specimen collection, specimen transport conditions, culture methodologies, and criteria for evaluation of culture outcomes was examined.
RESULTS: Twenty-five (93%) of 27 laboratories responded to the survey. Only two of 54 questions were answered uniformly by all responding laboratories. All laboratories reported vortexing or sonication of specimens before culture inoculation and centrifugation of inoculated cultures prior to incubation. In contrast, substantial variation was noted in specimen collection devices, specimen transport conditions and times, culture format, culture procedures, and criteria for identifying positive cultures.
CONCLUSION: Although this study did not evaluate the sensitivity of chlamydia cell cultures performed in different laboratories, there was substantial laboratory to laboratory variation in nearly every facet of culture evaluated. Laboratory to laboratory variation in chlamydia cell culture sensitivity likely accounts for part of the substantial variability in published evaluations of the sensitivity of nonculture chlamydia diagnostic tests.

Entities:  

Mesh:

Year:  1995        PMID: 7502188     DOI: 10.1097/00007435-199509000-00010

Source DB:  PubMed          Journal:  Sex Transm Dis        ISSN: 0148-5717            Impact factor:   2.830


  8 in total

Review 1.  Chlamydia screening: which sample for which technique?

Authors:  A Stary
Journal:  Genitourin Med       Date:  1997-04

2.  Differences in the sensitivity of the Amplicor Chlamydia trachomatis PCR assay.

Authors:  J M Ossewaarde; G J van Doornum; M Buimer; B Choueiri; A Stary
Journal:  Genitourin Med       Date:  1997-06

3.  Multicenter evaluation of the BDProbeTec ET System for detection of Chlamydia trachomatis and Neisseria gonorrhoeae in urine specimens, female endocervical swabs, and male urethral swabs.

Authors:  B Van Der Pol; D V Ferrero; L Buck-Barrington; E Hook; C Lenderman; T Quinn; C A Gaydos; J Lovchik; J Schachter; J Moncada; G Hall; M J Tuohy; R B Jones
Journal:  J Clin Microbiol       Date:  2001-03       Impact factor: 5.948

4.  Recommendations for the laboratory-based detection of Chlamydia trachomatis and Neisseria gonorrhoeae--2014.

Authors: 
Journal:  MMWR Recomm Rep       Date:  2014-03-14

5.  Evaluation of nucleic acid amplification tests as reference tests for Chlamydia trachomatis infections in asymptomatic men.

Authors:  R E Johnson; T A Green; J Schachter; R B Jones; E W Hook; C M Black; D H Martin; M E St Louis; W E Stamm
Journal:  J Clin Microbiol       Date:  2000-12       Impact factor: 5.948

6.  Relative accuracy of nucleic acid amplification tests and culture in detecting Chlamydia in asymptomatic men.

Authors:  H Cheng; M Macaluso; S H Vermund; E W Hook
Journal:  J Clin Microbiol       Date:  2001-11       Impact factor: 5.948

Review 7.  Sexually transmitted diseases in sexually abused children: medical and legal implications.

Authors:  M R Hammerschlag
Journal:  Sex Transm Infect       Date:  1998-06       Impact factor: 3.519

8.  Head-to-head multicenter comparison of DNA probe and nucleic acid amplification tests for Chlamydia trachomatis infection in women performed with an improved reference standard.

Authors:  Carolyn M Black; Jeanne Marrazzo; Robert E Johnson; Edward W Hook; Robert B Jones; Timothy A Green; Julius Schachter; Walter E Stamm; Gail Bolan; Michael E St Louis; David H Martin
Journal:  J Clin Microbiol       Date:  2002-10       Impact factor: 5.948

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.