Literature DB >> 7789285

Drug therapies for sexually transmitted diseases. Clinical and economic considerations.

W R Bowie1.   

Abstract

Sexually transmitted diseases (STDs) are common, and result in immense social and economic costs. In some countries they have a major demographic impact. Because many STDs facilitate the transmission of HIV, the consequences of STDs are further increasing. At the same time, this association between STDs and HIV provides one of the ways in which drug therapy should be very cost effective. The perspective taken in this article is a societal one, and broader issues than those directly related to drug costs and benefits are discussed. However, it is the availability of drugs that has the potential to most quickly and most reliably make a major difference to overall health sector and societal costs as they relate to STDs. For those STDs for which curative therapy is available (particularly Neisseria gonorrhoeae, Chlamydia trachomatis, Treponema pallidum, and Trichomonas vaginalis) there have been large decreases in prevalence in many parts of the world. In contrast, those STDs for which curative therapy is not available (particularly HIV, genital herpes and genital human papillomavirus infection) have had stable or increasing prevalence. For these latter infections, each new case increases the overall prevalence. Numerous features of STDs make clinical and economic evaluation difficult. These include the sensitive nature of the topic, the changing epidemiology and drug susceptibility of individual STDs, the fact that a large proportion of those infected are asymptomatic, difficulties in making specific diagnoses, the fact that often consequences are recognised late, sexual re-exposure and reinfection, and inadequate data on which to do clinical and economic evaluations. Furthermore, risk of acquiring an STD roughly correlates inversely with socioeconomic status, and countries or places with the highest rates of STDs may have the least ability to deal effectively with their diagnosis and management. Most of the direct and indirect costs are incurred by women, since they experience the vast majority of the complications of STDs. Many of these only become apparent years later, which makes it very hard to attribute costs and benefits to a specific episode of infection, and to its treatment. The late and indirect costs, plus the costs of prevention, are hard to quantify. That the major burden of STDs is in adolescents and young adults, socioeconomically disadvantaged groups and women has important implications, including for pharmacoeconomic studies.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1995        PMID: 7789285     DOI: 10.2165/00003495-199549040-00002

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  118 in total

1.  Efficiency and cost-effectiveness of field follow-up for patients with Chlamydia trachomatis infection in a sexually transmitted diseases clinic.

Authors:  B P Katz; C S Danos; T S Quinn; V Caine; R B Jones
Journal:  Sex Transm Dis       Date:  1988 Jan-Mar       Impact factor: 2.830

2.  Cost-effectiveness of culturing for Chlamydia trachomatis. A study in a clinic for sexually transmitted diseases.

Authors:  M D Nettleman; R B Jones; S D Roberts; B P Katz; A E Washington; R S Dittus; T S Quinn
Journal:  Ann Intern Med       Date:  1986-08       Impact factor: 25.391

3.  Azithromycin in the treatment of sexually transmitted disease.

Authors:  O Steingrimsson; J H Olafsson; H Thorarinsson; R W Ryan; R B Johnson; R C Tilton
Journal:  J Antimicrob Chemother       Date:  1990-01       Impact factor: 5.790

4.  Adverse reactions in a dose-ranging study with a new long-acting fluoroquinolone, fleroxacin.

Authors:  W R Bowie; V Willetts; P J Jewesson
Journal:  Antimicrob Agents Chemother       Date:  1989-10       Impact factor: 5.191

Review 5.  The impact of HIV and other STDs on human populations. Are predictions possible?

Authors:  M C Boily; R C Brunham
Journal:  Infect Dis Clin North Am       Date:  1993-12       Impact factor: 5.982

6.  Update: barrier protection against HIV infection and other sexually transmitted diseases.

Authors: 
Journal:  MMWR Morb Mortal Wkly Rep       Date:  1993-08-06       Impact factor: 17.586

7.  Cost-effectiveness of screening women at moderate risk for genital infections caused by Chlamydia trachomatis.

Authors:  M D Nettleman; R B Jones
Journal:  JAMA       Date:  1988-07-08       Impact factor: 56.272

8.  Ceftriaxone for treatment of uncomplicated gonorrhea: routine use of a single 125-mg dose in a sexually transmitted disease clinic.

Authors:  H H Handsfield; E W Hook
Journal:  Sex Transm Dis       Date:  1987 Oct-Dec       Impact factor: 2.830

9.  Pelvic inflammatory disease and fertility. A cohort study of 1,844 women with laparoscopically verified disease and 657 control women with normal laparoscopic results.

Authors:  L Weström; R Joesoef; G Reynolds; A Hagdu; S E Thompson
Journal:  Sex Transm Dis       Date:  1992 Jul-Aug       Impact factor: 2.830

10.  Chlamydia trachomatis, infertility, and population growth in sub-Saharan Africa.

Authors:  R C Brunham; M Cheang; J McMaster; G Garnett; R Anderson
Journal:  Sex Transm Dis       Date:  1993 May-Jun       Impact factor: 2.830

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  1 in total

1.  Cost effectiveness analysis of azithromycin and doxycycline for Chlamydia trachomatis infection in women: A Canadian perspective.

Authors:  F Marra; C A Marra; D M Patrick
Journal:  Can J Infect Dis       Date:  1997-07
  1 in total

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