Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
J Acquir Immune Defic Syndr. 2010 Dec;55 Suppl 2(Suppl 2):S136-40. doi: 10.1097/QAI.0b013e3181fbcb61.
The design of studies evaluating the safety and efficacy of interventions for HIV prevention is challenging in the US context, where there is low generalized prevalence. HIV incidence is sufficiently high in the at-risk US population of men who have sex with men that prevention trials using HIV infection end points are feasible. In other US populations at higher risk of HIV exposure, efficacy trials of HIV prevention are likely not feasible. However, for interventions where efficacy is already established, conducting trials that test different implementation strategies in these populations could provide definitive evidence about how to achieve high levels of coverage.
在美国,由于普遍流行率较低,评估 HIV 预防干预措施的安全性和有效性的研究设计具有挑战性。在美国男男性行为者这一高危人群中,HIV 发病率足够高,因此使用 HIV 感染终点的预防试验是可行的。在其他 HIV 暴露风险较高的美国人群中,HIV 预防的疗效试验可能不可行。然而,对于已经证实有效的干预措施,在这些人群中开展测试不同实施策略的试验,可以提供关于如何实现高覆盖率的明确证据。