Department of Medicine, University of Toronto, Toronto, ON, Canada.
Institute of Medical Sciences, University of Toronto, Toronto, ON, Canada.
J Int AIDS Soc. 2021 Jul;24 Suppl 3(Suppl 3):e25739. doi: 10.1002/jia2.25739.
HIV epidemic appraisals are used to characterize heterogeneity and inequities in the context of the HIV pandemic and the response. However, classic measures used in appraisals have been shown to underestimate disproportionate risks of onward transmission, particularly among key populations. In response, a growing number of modelling studies have quantified the consequences of unmet prevention and treatment needs (prevention gaps) among key populations as a transmission population attributable fraction over time (tPAF ). To aid its interpretation and use by programme implementers and policy makers, we outline and discuss a conceptual framework for understanding and estimating the tPAF via transmission modelling as a measure of onward transmission risk from HIV prevention gaps; and discuss properties of the tPAF .
The distribution of onward transmission risks may be defined by who is at disproportionate risk of onward transmission, and under which conditions. The latter reflects prevention gaps, including secondary prevention via treatment: the epidemic consequences of which may be quantified by the tPAF . Steps to estimating the tPAF include parameterizing the acquisition and onward transmission risks experienced by the subgroup of interest, defining the most relevant counterfactual scenario, and articulating the time-horizon of analyses and population among whom to estimate the relative difference in cumulative transmissions; such steps could reflect programme-relevant questions about onward transmission risks. Key properties of the tPAF include larger onward transmission risks over longer time-horizons; seemingly mutually exclusive tPAF measures summing to greater than 100%; an opportunity to quantify the magnitude of disproportionate onward transmission risks with a per-capita tPAF ; and that estimates are conditional on what has been achieved so far in reducing prevention gaps and maintaining those conditions moving forward as the status quo.
The next generation of HIV epidemic appraisals has the potential to support a more specific HIV response by characterizing heterogeneity in disproportionate risks of onward transmission which are defined and conditioned on the past, current and future prevention gaps across subsets of the population.
HIV 疫情评估用于描述 HIV 大流行背景下和应对措施中的异质性和不平等现象。然而,评估中使用的经典指标已被证明低估了特定人群中传播风险不成比例的情况。为应对这一问题,越来越多的模型研究已量化了特定人群中未满足的预防和治疗需求(预防差距)作为传播人群归因分数(tPAF)随时间的变化情况。为帮助方案执行者和政策制定者理解和使用这一指标,我们提出并讨论了一个概念框架,用于通过传播建模来理解和估计 tPAF,将其作为衡量 HIV 预防差距导致的传播风险的指标,并讨论了 tPAF 的属性。
传播风险的分布情况可以由具有不成比例的传播风险的人群以及他们所处的环境来定义。后者反映了预防差距,包括通过治疗实现的二级预防:其流行后果可以通过 tPAF 来量化。估计 tPAF 的步骤包括:对相关亚组所经历的获得和传播风险进行参数化,定义最相关的反事实情况,并阐明分析的时间范围和要估计累积传播差异的人群;这些步骤可能反映了与方案相关的有关传播风险的问题。tPAF 的主要属性包括:时间范围越长,传播风险越大;看似相互排斥的 tPAF 指标加起来超过 100%;有机会通过人均 tPAF 量化不成比例的传播风险的大小;以及估计结果取决于迄今为止在减少预防差距方面取得的进展,并在未来保持这些条件,以维持现状。
下一代 HIV 疫情评估有可能通过描述不成比例的传播风险的异质性来支持更具体的 HIV 应对措施,这些风险是根据人口亚组的过去、现在和未来的预防差距来定义和限定的。