Literature DB >> 15918786

Treatment of chancroid in resource-poor countries.

Naa Torshie Annan1, David A Lewis.   

Abstract

Chancroid, formerly a major cause of the genital ulcer disease syndrome, remains an important cofactor in both the transmission and acquisition of HIV-1 infection. Those countries with the greatest burden of HIV also have some of the highest prevalence rates of chancroid worldwide. The diagnosis of chancroid, caused by the fastidious bacterium Haemophilus ducreyi, is both expensive and difficult in many resource-poor areas. These areas of the world use syndromic management to treat genital ulcers and such an approach has proven effective in reducing rates of bacterial genital ulcer diseases. There are currently inexpensive and effective single-dose therapies available to treat chancroid. Single-dose regimens, given at first presentation, improve compliance and reduce the risk of sexually transmitted infections. Bacterial resistance to several antimicrobial agents has increased over the years and remains a continued threat to effective antimicrobial therapy. Follow-up of cases, and partner notification and treatment is carried out to limit reinfection and onward transmission of chancroid. Patients with coexistent HIV may be particularly at risk of failing single-dose therapy and should therefore be reviewed wherever possible.

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Year:  2005        PMID: 15918786     DOI: 10.1586/14787210.3.2.295

Source DB:  PubMed          Journal:  Expert Rev Anti Infect Ther        ISSN: 1478-7210            Impact factor:   5.091


  4 in total

1.  Passive immunization with a polyclonal antiserum to the hemoglobin receptor of Haemophilus ducreyi confers protection against a homologous challenge in the experimental swine model of chancroid.

Authors:  Isabelle Leduc; William G Fusco; Neelima Choudhary; Patty A Routh; Deborah M Cholon; Marcia M Hobbs; Glen W Almond; Paul E Orndorff; Christopher Elkins
Journal:  Infect Immun       Date:  2011-06-06       Impact factor: 3.441

2.  Haemophilus ducreyi SapA contributes to cathelicidin resistance and virulence in humans.

Authors:  Kristy L B Mount; Carisa A Townsend; Sherri D Rinker; Xiaoping Gu; Kate R Fortney; Beth W Zwickl; Diane M Janowicz; Stanley M Spinola; Barry P Katz; Margaret E Bauer
Journal:  Infect Immun       Date:  2010-01-19       Impact factor: 3.441

3.  The Hd0053 gene of Haemophilus ducreyi encodes an alpha2,3-sialyltransferase.

Authors:  Yanhong Li; Mingchi Sun; Shengshu Huang; Hai Yu; Harshal A Chokhawala; Vireak Thon; Xi Chen
Journal:  Biochem Biophys Res Commun       Date:  2007-07-23       Impact factor: 3.575

4.  Phosphoethanolamine Transferase LptA in Haemophilus ducreyi Modifies Lipid A and Contributes to Human Defensin Resistance In Vitro.

Authors:  Michael P Trombley; Deborah M B Post; Sherri D Rinker; Lorri M Reinders; Kate R Fortney; Beth W Zwickl; Diane M Janowicz; Fitsum M Baye; Barry P Katz; Stanley M Spinola; Margaret E Bauer
Journal:  PLoS One       Date:  2015-04-22       Impact factor: 3.240

  4 in total

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