Literature DB >> 10023349

Comparison of clinically directed, disease specific, and syndromic protocols for the management of genital ulcer disease in Lesotho.

Y Htun1, S A Morse, Y Dangor, G Fehler, F Radebe, D L Trees, C M Beck-Sague, R C Ballard.   

Abstract

OBJECTIVE: To evaluate two protocols for the syndromic management of genital ulcer disease (GUD) in Lesotho, southern Africa and to compare the performance of these protocols with that of a conventional disease specific approach.
METHODS: A cross sectional study was conducted among consecutive patients with GUD attending an STD clinic in Maseru, Lesotho. The clinical diagnoses were made by using predefined criteria at the initial visit before the performance of laboratory tests. Attempts were made to detect the specific aetiology of the genital ulcers using PCR assays and syphilis serology. The results of PCR assays and syphilis serology were used as the gold standard against which the performance of the management approaches were applied.
RESULTS: Of 100 patients initially recruited into the study, Haemophilus ducreyi infection was detected in 56%, herpes simplex virus in 26%, Treponema pallidum in 23%, and lymphogranuloma venereum in 7%. No pathogens were detected in 6% of patients. 17% of patients had mixed infections. Sensitivity, specificity, positive and negative predictive values of the three management protocols for GUD were compared after applying each to the study population. Theoretically, the lowest correct treatment rate would have been obtained by using the disease specific protocol (62%) compared with more than 90% in both syndromic management protocols. Considerable overtreatment for primary syphilis would occur following application of both syndromic protocols. This would be the result of the overdiagnosis of chancroid, in particular the misdiagnosis of genital herpes as chancroid, which would receive treatment for syphilis unnecessarily. The HIV seroprevalence among these patients was 36%. A significantly higher rate of HIV seropositivity was detected among the patients with herpes simplex virus infection when compared with those patients having other causes of genital ulcer disease (58% v 27%; odds ratio 3.73; 95% CI 1.26-11.26; p = 0.01).
CONCLUSIONS: Poor sensitivity, specificity, and predictive values were recorded when the disease specific protocol was applied to the study population. In contrast, the syndromic management protocols provided adequate treatment for more than 90% of patients with GUD. Protocol C, which identified a minority of cases of genital herpes, was found to have an advantage when compared with protocol B (all patients with genital ulcer disease treated for both syphilis and chancroid) in that 29% of genital herpes cases would receive appropriate counselling.

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Year:  1998        PMID: 10023349

Source DB:  PubMed          Journal:  Sex Transm Infect        ISSN: 1368-4973            Impact factor:   3.519


  12 in total

Review 1.  Increasing prevalence of genital herpes in developing countries: implications for heterosexual HIV transmission and STI control programmes.

Authors:  N O'Farrell
Journal:  Sex Transm Infect       Date:  1999-12       Impact factor: 3.519

2.  The Use of Molecular Techniques for the Diagnosis and Epidemiologic Study of Sexually Transmitted Infections.

Authors: 
Journal:  Curr Infect Dis Rep       Date:  2000-02       Impact factor: 3.725

Review 3.  Lymphogranuloma venereum.

Authors:  D Mabey; R W Peeling
Journal:  Sex Transm Infect       Date:  2002-04       Impact factor: 3.519

Review 4.  Comparison of Diagnostic Accuracy of PCR Targeting the 47-Kilodalton Protein Membrane Gene of Treponema pallidum and PCR Targeting the DNA Polymerase I Gene: Systematic Review and Meta-analysis.

Authors:  Angèle Gayet-Ageron; Christophe Combescure; Stephan Lautenschlager; Béatrice Ninet; Thomas V Perneger
Journal:  J Clin Microbiol       Date:  2015-08-26       Impact factor: 5.948

5.  Aetiology of sexually transmitted infections and response to syndromic treatment in southwest Uganda.

Authors:  J M Pickering; J A G Whitworth; P Hughes; M Kasse; D Morgan; B Mayanja; L Van der Paal; P Mayaud
Journal:  Sex Transm Infect       Date:  2005-12       Impact factor: 3.519

6.  Diagnosing genital ulcer disease in a clinic for sexually transmitted diseases in Amsterdam, The Netherlands.

Authors:  S M Bruisten; I Cairo; H Fennema; A Pijl; M Buimer; P G Peerbooms; E Van Dyck ; A Meijer; J M Ossewaarde; G J van Doornum
Journal:  J Clin Microbiol       Date:  2001-02       Impact factor: 5.948

7.  Etiology of genital ulcer disease in Dakar, Senegal, and comparison of PCR and serologic assays for detection of Haemophilus ducreyi.

Authors:  P A Totten; J M Kuypers; C Y Chen; M J Alfa; L M Parsons; S M Dutro; S A Morse; N B Kiviat
Journal:  J Clin Microbiol       Date:  2000-01       Impact factor: 5.948

Review 8.  Chancroid: clinical manifestations, diagnosis, and management.

Authors:  D A Lewis
Journal:  Sex Transm Infect       Date:  2003-02       Impact factor: 3.519

9.  Association of age at first sex with HIV-1, HSV-2, and other sexual transmitted infections among women in northern Tanzania.

Authors:  Musie Ghebremichael; Ulla Larsen; Elijah Paintsil
Journal:  Sex Transm Dis       Date:  2009-09       Impact factor: 2.830

10.  Lack of utility of risk score and gynecological examination for screening for sexually transmitted infections in sexually active adolescents.

Authors:  Eleuse M B Guimarães; Mark D C Guimarães; Maria Aparecida S Vieira; Nádia M Bontempo; Mirian S S Seixas; Mônica S D Garcia; Lyana E S Daud; Rejane L M Côrtes; Maria de Fátima C Alves
Journal:  BMC Med       Date:  2009-03-11       Impact factor: 8.775

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