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Men at risk of gonococcal urethritis: a case-control study in a Darwin sexual health clinic

BACKGROUND: Male urethritis is primary sexually transmitted. Northern Territory (NT) has the highest rates of gonococcal infection in Australia and local guidelines recommend empiric treatment with azithromycin and ceftriaxone for all men presenting with urethritis. As gonococcal drug resistance is...

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Autores principales: Chen, Winnie, Connor, Suzanne, Gunathilake, Manoji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873514/
https://www.ncbi.nlm.nih.gov/pubmed/31752720
http://dx.doi.org/10.1186/s12879-019-4625-8
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author Chen, Winnie
Connor, Suzanne
Gunathilake, Manoji
author_facet Chen, Winnie
Connor, Suzanne
Gunathilake, Manoji
author_sort Chen, Winnie
collection PubMed
description BACKGROUND: Male urethritis is primary sexually transmitted. Northern Territory (NT) has the highest rates of gonococcal infection in Australia and local guidelines recommend empiric treatment with azithromycin and ceftriaxone for all men presenting with urethritis. As gonococcal drug resistance is a growing concern, this study aims to improve empiric use of ceftriaxone through examining local patterns of male urethritis, comparing cases of gonococcal urethritis (GU) to controls with non-gonococcal urethritis (NGU). METHODS: A retrospective study was undertaken of all men with symptomatic urethritis presenting to Darwin sexual health clinic from July 2015 to July 2016 and aetiology of urethritis in this population was described. Demographic, risk profile, and clinical features of GU cases were compared to NGU controls. RESULTS: Among n = 145 men, the most common organisms identified were Chlamydia trachomatis (23.4%, SE 3.5%) and Neisseria gonorrhoeae (17.2%, SE 3.1%). The main predictors of GU were any abnormalities on genital examination (aOR 10.4, 95% CI 2.1 to 50.8) and a history of urethral discharge (aOR 5.7, 95% CI 1.4 to 22.6). Aboriginal patients (aOR 3.0, 95% CI 0.9 to 9.6) and those over 30 years of age (aOR 1.4, 95% CI 0.3 to 7.0) were more likely to have GU in the unadjusted analysis, but not in the adjusted model. CONCLUSION: This is the first study looking at patterns of male urethritis in urban NT and the results support a move towards adopting national guidelines to use ceftriaxone for empiric management of syndromic urethritis only in high-risk patients. In addition to traditional demographic risk factors, clinical features remain an important component of risk stratification.
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spelling pubmed-68735142019-12-12 Men at risk of gonococcal urethritis: a case-control study in a Darwin sexual health clinic Chen, Winnie Connor, Suzanne Gunathilake, Manoji BMC Infect Dis Research Article BACKGROUND: Male urethritis is primary sexually transmitted. Northern Territory (NT) has the highest rates of gonococcal infection in Australia and local guidelines recommend empiric treatment with azithromycin and ceftriaxone for all men presenting with urethritis. As gonococcal drug resistance is a growing concern, this study aims to improve empiric use of ceftriaxone through examining local patterns of male urethritis, comparing cases of gonococcal urethritis (GU) to controls with non-gonococcal urethritis (NGU). METHODS: A retrospective study was undertaken of all men with symptomatic urethritis presenting to Darwin sexual health clinic from July 2015 to July 2016 and aetiology of urethritis in this population was described. Demographic, risk profile, and clinical features of GU cases were compared to NGU controls. RESULTS: Among n = 145 men, the most common organisms identified were Chlamydia trachomatis (23.4%, SE 3.5%) and Neisseria gonorrhoeae (17.2%, SE 3.1%). The main predictors of GU were any abnormalities on genital examination (aOR 10.4, 95% CI 2.1 to 50.8) and a history of urethral discharge (aOR 5.7, 95% CI 1.4 to 22.6). Aboriginal patients (aOR 3.0, 95% CI 0.9 to 9.6) and those over 30 years of age (aOR 1.4, 95% CI 0.3 to 7.0) were more likely to have GU in the unadjusted analysis, but not in the adjusted model. CONCLUSION: This is the first study looking at patterns of male urethritis in urban NT and the results support a move towards adopting national guidelines to use ceftriaxone for empiric management of syndromic urethritis only in high-risk patients. In addition to traditional demographic risk factors, clinical features remain an important component of risk stratification. BioMed Central 2019-11-21 /pmc/articles/PMC6873514/ /pubmed/31752720 http://dx.doi.org/10.1186/s12879-019-4625-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Chen, Winnie
Connor, Suzanne
Gunathilake, Manoji
Men at risk of gonococcal urethritis: a case-control study in a Darwin sexual health clinic
title Men at risk of gonococcal urethritis: a case-control study in a Darwin sexual health clinic
title_full Men at risk of gonococcal urethritis: a case-control study in a Darwin sexual health clinic
title_fullStr Men at risk of gonococcal urethritis: a case-control study in a Darwin sexual health clinic
title_full_unstemmed Men at risk of gonococcal urethritis: a case-control study in a Darwin sexual health clinic
title_short Men at risk of gonococcal urethritis: a case-control study in a Darwin sexual health clinic
title_sort men at risk of gonococcal urethritis: a case-control study in a darwin sexual health clinic
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873514/
https://www.ncbi.nlm.nih.gov/pubmed/31752720
http://dx.doi.org/10.1186/s12879-019-4625-8
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