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Evaluation of a direct immunofluorescence test for diagnosing gonorrhea


, : Evaluation of a direct immunofluorescence test for diagnosing gonorrhea. Journal of Clinical Pathology (London) 38(10): 1142-1145

A new direct immunofluorescence reagent (Syva and Genetic Systems Inc) was evaluated for its ability to detect Neisseria gonorrhoeae in specimens from populations with a high prevalence of the infection. Gonorrhoea was diagnosed by culture in 45 of 105 (43%) urethral specimens from men and 17 of 90 (28%) urethral and 25 of 60 (42%) cervical specimens from women. In men the immunofluorescence test had a sensitivity of 84.4% and specificity of 100%; Gram staining gave values of 94% and 100%, respectively. The sensitivity of the immunofluorescence test could be increased to 89% by testing duplicate smeass. In women the immunofluorescence test had a sensitivity of 65% and a specificity of 98% for urethral samples and values of 72% and 94%, respectivley for cervical samples. At both sites the sensitivity of the Gram stain was 40% and the specificity to 76% for urethral and 88% for cervical samples.

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Accession: 005395070

PMID: 3932488

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Related references

Ison, C.A.; McLean, K.; Gedney, J.; Munday, P.E.; Coghill, D.; Smith, R.; Harris, J.R.; Easmon, C.S., 1985: Evaluation of a direct immunofluorescence test for diagnosing gonorrhoea. A new direct immunofluorescence reagent (Syva and Genetic Systems Inc) was evaluated for its ability to detect Neisseria gonorrhoeae in specimens from populations with a high prevalence of the infection. Gonorrhoea was diagnosed by culture in 45 o...

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