Okwundu Charles I, Uthman Olalekan A, Okoromah Christy An
Centre for Evidence-Based Health Care, Faculty of Health Sciences, Stellenbosch University, Tygerberg, South Africa.
Cochrane Database Syst Rev. 2012 Jul 11;2012(7):CD007189. doi: 10.1002/14651858.CD007189.pub3.
More than 30 years into the global HIV/AIDS epidemic, infection rates remain alarmingly high, with over 2.7 million people becoming infected every year. There is a need for HIV prevention strategies that are more effective. Oral antiretroviral pre-exposure prophylaxis (PrEP) in high-risk individuals may be a reliable tool in preventing the transmission of HIV.
To evaluate the effects of oral antiretroviral chemoprophylaxis in preventing HIV infection in HIV-uninfected high-risk individuals.
We revised the search strategy from the previous version of the review and conducted an updated search of MEDLINE, the Cochrane Central Register of Controlled Trials and EMBASE in April 2012. We also searched the WHO International Clinical Trials Registry Platform and ClinicalTrials.gov for ongoing trials.
Randomised controlled trials that evaluated the effects of any antiretroviral agent or combination of antiretroviral agents in preventing HIV infection in high-risk individuals
Data concerning outcomes, details of the interventions, and other study characteristics were extracted by two independent authors using a standardized data extraction form. Relative risk with a 95% confidence interval (CI) was used as the measure of effect.
We identified 12 randomised controlled trials that meet the criteria for the review. Six were ongoing trials, four had been completed and two had been terminated early. Six studies with a total of 9849 participants provided data for this review. The trials evaluated the following: daily oral tenofovir disoproxil fumarate (TDF) plus emtricitabine (FTC) versus placebo; TDF versus placebo and daily TDF-FTC versus intermittent TDF-FTC. One of the trials had three study arms: TDF, TDF-FTC and placebo arm. The studies were carried out amongst different risk groups, including HIV-uninfected men who have sex with men, serodiscordant couples and other high risk men and women.Overall results from the four trials that compared TDF-FTC versus placebo showed a reduction in the risk of acquiring HIV infection (RR 0.51; 95% CI 0.30 to 0.86; 8918 participants). Similarly, the overall results of the studies that compared TDF only versus placebo showed a significant reduction in the risk of acquiring HIV infection (RR 0.38; 95% CI 0.23 to 0.63, 4027 participants). There were no significant differences in the risk of adverse events across all the studies that reported on adverse events. Also, adherence and sexual behaviours were similar in both the intervention and control groups.
AUTHORS' CONCLUSIONS: Finding from this review suggests that pre-exposure prophylaxis with TDF alone or TDF-FTC reduces the risk of acquiring HIV in high-risk individuals including people in serodiscordant relationships, men who have sex with men and other high risk men and women.
全球艾滋病疫情已持续30多年,感染率仍然高得惊人,每年有超过270万人感染。需要更有效的艾滋病预防策略。对高危个体进行口服抗逆转录病毒药物暴露前预防(PrEP)可能是预防艾滋病传播的可靠工具。
评估口服抗逆转录病毒药物化学预防对未感染艾滋病的高危个体预防感染艾滋病的效果。
我们修订了上一版综述的检索策略,并于2012年4月对MEDLINE、Cochrane对照试验中央注册库和EMBASE进行了更新检索。我们还在世卫组织国际临床试验注册平台和ClinicalTrials.gov上搜索了正在进行的试验。
评估任何抗逆转录病毒药物或抗逆转录病毒药物组合对高危个体预防感染艾滋病效果的随机对照试验。
两名独立作者使用标准化数据提取表提取有关结局、干预细节和其他研究特征的数据。采用相对危险度及95%置信区间(CI)作为效应量度。
我们确定了12项符合综述标准的随机对照试验。6项为正在进行的试验,4项已完成,2项提前终止。6项研究共9849名参与者为本综述提供了数据。这些试验评估了以下内容:每日口服替诺福韦酯(TDF)加恩曲他滨(FTC)与安慰剂对比;TDF与安慰剂对比以及每日TDF-FTC与间歇TDF-FTC对比。其中一项试验有三个研究组:TDF组、TDF-FTC组和安慰剂组。这些研究在不同风险组中进行,包括未感染艾滋病的男男性行为者、血清学不一致的伴侣以及其他高危男性和女性。比较TDF-FTC与安慰剂的四项试验的总体结果显示,感染艾滋病的风险降低(相对危险度0.51;95%CI 0.30至0.86;8918名参与者)。同样,仅比较TDF与安慰剂的研究总体结果显示,感染艾滋病的风险显著降低(相对危险度0.38;95%CI 0.23至0.63,4027名参与者)。在所有报告不良事件的研究中,不良事件风险无显著差异。此外,干预组和对照组的依从性和性行为相似。
本综述结果表明,单独使用TDF或TDF-FTC进行暴露前预防可降低高危个体(包括血清学不一致关系中的人群、男男性行为者以及其他高危男性和女性)感染艾滋病的风险。