Validity of an enzyme immunoassay for detection of Neisseria gonorrhoeae antigens.
AUTOR(ES)
Papasian, C J
RESUMO
An enzyme immunoassay (EIA; Gonozyme, Abbott Laboratories) for the antigenic detection of Neisseria gonorrhoeae in endocervical or urethral specimens was evaluated. EIA results were compared with results of conventional culture tests for N. gonorrhoeae. Specimens from 208 males (113 culture positive) and 252 females (72 culture positive) were tested. The sensitivity and specificity of EIA for specimens from males were 97.3 and 95.8%, respectively. The sensitivity and specificity of EIA for specimens from females were 79.2 and 87.2%, respectively.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=271062Documentos Relacionados
- Modified enzyme immunoassay for detecting Neisseria gonorrhoeae antigens.
- Detection of Neisseria gonorrhoeae antigen by a solid-phase enzyme immunoassay.
- Comparison of the PREMIER cryptococcal antigen enzyme immunoassay and the latex agglutination assay for detection of cryptococcal antigens.
- Development of an enzyme immunoassay for poliovirus antigens
- Detection of Chlamydia trachomatis and Neisseria gonorrhoeae by Enzyme Immunoassay, Culture, and Three Nucleic Acid Amplification Tests