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Evaluation of serological diagnostic tests for human Brucellosis in an endemic area
Abstract
Objectives: The clinical utility of complementary tests for brucellosis are not clear in many situation. This study aimed to evaluate value of these tests for brucellosis in an endemic area in Turkey. Materials and methods: This study was performed at Çanakkale General Hospital in 2009. In a retrospective approach, records of the patients who evaluated for brucellosis were collected. During the study period, 236 people (131 symptomatic and 105 non-symptomatic) were evaluated for diagnosis of brucellosis. All of the samples from these patients were tested for Brucella antibody seropositivity by RB slide agglutination, standard serum agglutination, Brucella Coombs, BrucellaCapt, and ELISA IgG and IgM tests. Results: In total, 49 symptomatic patients were hospitalized and blood cultures were obtained. Brucella spp. were isolated from nine of them (18.4%).The BrucellaCapt test was found to be the most sensitive for Brucella (74.0%) and close behind it was the Coombs test (72.5%). The sensitivity for the RB test was 48.1%. The ELISA IgG test was found more sensitive for brucellosis than the ELISA IgM test was (65.6% and 49.6%, respectively). All examined tests were found about 100% specific for brucellosis but the RB test was found less specific than the others were (96.1%) Positive predictive value for all tests was about 1 but negative predictive values were only valuable for the Coombs and Brucella Capt test (0.744 and 0.755, respectively). The other serological tests were around and below 0.50, which was weak for negative results. Conclusions: The ELISA IgG and IgM tests were no superior to the other tests. By assessment of receiver operating characteristics (ROC) analysis, the Brucella Coombs and BrucellaCapt tests were found to be the most valuable tests for serological diagnosis of brucellosis in endemic areas. The seronegative tests in the symptomatic patients should be evaluated and repeated in short time.
Keywords
References
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Details
Primary Language
English
Subjects
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Journal Section
-
Publication Date
June 1, 2012
Submission Date
April 30, 2015
Acceptance Date
-
Published in Issue
Year 2012 Volume: 2 Number: 02
APA
Arabacı, F., & Oldacay, M. (2012). Evaluation of serological diagnostic tests for human Brucellosis in an endemic area. Journal of Microbiology and Infectious Diseases, 2(02), 50-56. https://doi.org/10.5799/ahinjs.02.2012.02.0042
AMA
1.Arabacı F, Oldacay M. Evaluation of serological diagnostic tests for human Brucellosis in an endemic area. J Microbil Infect Dis. 2012;2(02):50-56. doi:10.5799/ahinjs.02.2012.02.0042
Chicago
Arabacı, Filiz, and Mehmet Oldacay. 2012. “Evaluation of Serological Diagnostic Tests for Human Brucellosis in an Endemic Area”. Journal of Microbiology and Infectious Diseases 2 (02): 50-56. https://doi.org/10.5799/ahinjs.02.2012.02.0042.
EndNote
Arabacı F, Oldacay M (June 1, 2012) Evaluation of serological diagnostic tests for human Brucellosis in an endemic area. Journal of Microbiology and Infectious Diseases 2 02 50–56.
IEEE
[1]F. Arabacı and M. Oldacay, “Evaluation of serological diagnostic tests for human Brucellosis in an endemic area”, J Microbil Infect Dis, vol. 2, no. 02, pp. 50–56, June 2012, doi: 10.5799/ahinjs.02.2012.02.0042.
ISNAD
Arabacı, Filiz - Oldacay, Mehmet. “Evaluation of Serological Diagnostic Tests for Human Brucellosis in an Endemic Area”. Journal of Microbiology and Infectious Diseases 2/02 (June 1, 2012): 50-56. https://doi.org/10.5799/ahinjs.02.2012.02.0042.
JAMA
1.Arabacı F, Oldacay M. Evaluation of serological diagnostic tests for human Brucellosis in an endemic area. J Microbil Infect Dis. 2012;2:50–56.
MLA
Arabacı, Filiz, and Mehmet Oldacay. “Evaluation of Serological Diagnostic Tests for Human Brucellosis in an Endemic Area”. Journal of Microbiology and Infectious Diseases, vol. 2, no. 02, June 2012, pp. 50-56, doi:10.5799/ahinjs.02.2012.02.0042.
Vancouver
1.Filiz Arabacı, Mehmet Oldacay. Evaluation of serological diagnostic tests for human Brucellosis in an endemic area. J Microbil Infect Dis. 2012 Jun. 1;2(02):50-6. doi:10.5799/ahinjs.02.2012.02.0042
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