Rush to judgment: the STI-treatment trials and HIV in sub-Saharan Africa

被引:12
|
作者
Stillwaggon, Eileen [1 ]
Sawers, Larry [2 ]
机构
[1] Gettysburg Coll, Dept Econ, Gettysburg, PA 17325 USA
[2] Amer Univ, Dept Econ, Washington, DC 20016 USA
关键词
HIV; AIDS; RCT; STI; sub-Saharan Africa; sexually transmitted disease and HIV; randomized controlled trial; SEXUALLY-TRANSMITTED-DISEASES; FEMALE GENITAL SCHISTOSOMIASIS; IMMUNODEFICIENCY-VIRUS TYPE-1; PUBLIC-HEALTH; BACTERIAL VAGINOSIS; SYNDROMIC TREATMENT; SEX WORKERS; RANDOMIZED TRIAL; VAGINAL FLORA; RISK-FACTORS;
D O I
10.7448/IAS.18.1.19844
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: The extraordinarily high incidence of HIV in sub-Saharan Africa led to the search for cofactor infections that could explain the high rates of transmission in the region. Genital inflammation and lesions caused by sexually transmitted infections (STIs) were a probable mechanism, and numerous observational studies indicated several STI cofactors. Nine out of the ten randomized controlled trials (RCTs), however, failed to demonstrate that treating STIs could lower HIV incidence. We evaluate all 10 trials to determine if their design permits the conclusion, widely believed, that STI treatment is ineffective in reducing HIV incidence. Discussion: Examination of the trials reveals critical methodological problems sufficient to account for statistically insignificant outcomes in nine of the ten trials. Shortcomings of the trials include weak exposure contrast, confounding, non-differential misclassification, contamination and effect modification, all of which consistently bias the results toward the null. In any future STI-HIV trial, ethical considerations will again require weak exposure contrast. The complexity posed by HIV transmission in the genital microbial environment means that any future STI-HIV trial will face confounding, non-differential misclassification and effect modification. As a result, it is unlikely that additional trials would be able to answer the question of whether STI control reduces HIV incidence. Conclusions: Shortcomings in published RCTs render invalid the conclusion that treating STIs and other cofactor infections is ineffective in HIV prevention. Meta-analyses of observational studies conclude that STIs can raise HIV transmission efficiency two-to fourfold. Health policy is always implemented under uncertainty. Given the known benefits of STI control, the irreparable harm from not treating STIs and the likely decline in HIV incidence resulting from STI control, it is appropriate to expand STI control programmes and to use funds earmarked for HIV prevention to finance those programmes.
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页数:9
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