Evaluation of the Roche cobas® CT/NG Test for Detection of Chlamydia trachomatis and Neisseria gonorrhoeae in Male Urine

2012 ◽  
Vol 39 (7) ◽  
pp. 543-549 ◽  
Author(s):  
Stephanie N. Taylor ◽  
Oliver Liesenfeld ◽  
Rebecca A. Lillis ◽  
Barbara A. Body ◽  
Melinda Nye ◽  
...  
2011 ◽  
Vol 87 (Suppl 1) ◽  
pp. A278-A279
Author(s):  
A. Pantone ◽  
B. Van Der Pol ◽  
R. Lillis ◽  
B. Loyd ◽  
M. B. Nye ◽  
...  

2015 ◽  
Vol 118 ◽  
pp. 70-74 ◽  
Author(s):  
Dewi J. de Waaij ◽  
Jan Henk Dubbink ◽  
Remco P.H. Peters ◽  
Sander Ouburg ◽  
Servaas A. Morré

2019 ◽  
Vol 68 (2) ◽  
pp. 197-200 ◽  
Author(s):  
Abdessalam Cherkaoui ◽  
Gesuele Renzi ◽  
Michèle Mombelli ◽  
Katia Jaton ◽  
Sabine Yerly ◽  
...  

2019 ◽  
Vol 57 (4) ◽  
Author(s):  
Barbara Van Der Pol ◽  
Kenneth Fife ◽  
Stephanie N. Taylor ◽  
Melinda B. Nye ◽  
Steven E. Chavoustie ◽  
...  

ABSTRACT The clinical performance of the Cobas CT/NG assay on the Cobas 6800/8800 systems (Cobas) for the detection of Chlamydia trachomatis and Neisseria gonorrhoeae was established in a multisite, prospective collection study using male and female urogenital specimens; supportive data from archived specimens were also included. The results obtained with the Cobas assay were compared with the patient infected status derived from a combination of U.S. Food and Drug Administration-approved nucleic acid amplification tests to determine the sensitivity and specificity of detection from each sample type. The sensitivity of Cobas for the detection of C. trachomatis in female specimens was 95.6% (95% confidence interval [CI], 92.4% to 97.4%) for urine; 98.6% (95% CI, 95.2% to 99.6%) and 99.2% (95% CI, 95.4% to 99.9%) for clinician- and self-collected vaginal swab specimens, respectively; 93.3% (95% CI, 89.6% to 95.7%) for endocervical swabs; and 92.5% (95% CI, 88.7% to 95.1%) for cervical swab samples in PreservCyt. The specificity for the detection of C. trachomatis was ≥98.8% for all female sample types. Sensitivity and specificity estimates of Cobas for the detection of C. trachomatis in male urine samples were 100% (96.8% to 100.0%) and 99.7% (95% CI, 99.2% to 99.9%), respectively. The sensitivity of Cobas for the detection of N. gonorrhoeae in female specimens was 94.8% (95% CI, 89.6% to 97.4%) for urine; 100.0% (95% CI, 87.9% to 100.0%) and 100.0% (95% CI, 87.9% to 100.0%) for clinician- and self-collected vaginal swab specimens, respectively; 97.0% (95% CI, 91.5% to 99.0%) for endocervical swabs; and 96.6% (95% CI, 90.6% to 98.8%) for cervical samples in PreservCyt; the specificity for all female sample types was >99.0%. The sensitivity and specificity of Cobas for detecting N. gonorrhoeae in male urine were 100.0% (95% CI, 95.8% to 100.0%) and 99.5% (95% CI, 98.8% to 99.8%), respectively. Fully automated assays help fill the clinical need for a sensitive, high-throughput screening tool to aid public health efforts to control C. trachomatis and N. gonorrhoeae infections.


2005 ◽  
Vol 43 (1) ◽  
pp. 127-131 ◽  
Author(s):  
M. A. Chernesky ◽  
D. H. Martin ◽  
E. W. Hook ◽  
D. Willis ◽  
J. Jordan ◽  
...  

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