Division of Clinical of Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.
BMC Health Serv Res. 2010 Jul 2;10 Suppl 1(Suppl 1):S3. doi: 10.1186/1472-6963-10-S1-S3.
Despite concerns about affordability and sustainability, many models of the lifetime costs of antiretroviral therapy (ART) used in resource limited settings are based on data from small research cohorts, together with pragmatic assumptions about life-expectancy. This paper revisits these modelling assumptions in order to provide input to future attempts to model the lifetime costs and the costs of scaling up ART.
We analysed the determinants of costs and outcomes in patients receiving ART in line with standard World Health Organization (WHO) guidelines for resource poor settings in a private sector managed ART programme in South Africa. The cohort included over 5,000 patients with up to 4 years (median 19 months) on ART. Generalized linear and Cox proportional hazards regression models were used to establish cost and outcome determinants respectively.
The key variables associated with changes in mean monthly costs were: being on the second line regimen; receiving ART from 4 months prior to 4 months post treatment initiation; having a recent or current CD4 count <50 cells/microL or 50-199 cells/microl; having mean ART adherence <75% as determined by monthly pharmacy refill data; and having a current or recent viral load >100,000 copies/mL. In terms of the likelihood of dying, the key variables were: baseline CD4 count<50 cells/microl (particularly during the first 4 months on treatment); current CD4 count <50 cells/microl and 50-199 cells/microl (particularly during later periods on treatment); and being on the second line regimen. Being poorly adherent and having an unsuppressed viral load was also associated with a higher likelihood of dying.
While there are many unknowns associated with modelling the resources needed to scale-up ART, our analysis has suggested a number of key variables which can be used to improve the state of the art of modelling ART. While the magnitude of the effects associated with these variables would be likely to differ in other settings, the variables influencing costs and survival are likely to be generalizable. This is of direct relevance to those concerned about assessing the long-term costs and sustainability of expanded access to ART.
尽管人们对负担能力和可持续性表示担忧,但在资源有限的环境中使用的抗逆转录病毒疗法(ART)的终生成本模型大多基于来自小型研究队列的数据,并对预期寿命做出了务实的假设。本文重新审视了这些建模假设,以期为未来尝试对 ART 的终生成本和扩大规模的成本进行建模提供依据。
我们按照资源匮乏环境中世卫组织(WHO)的标准指南,在南非私营部门管理的 ART 方案中,对符合条件的患者进行了 ART 治疗,分析了影响其成本和结局的决定因素。该队列包括 5000 多名接受 ART 治疗长达 4 年(中位数 19 个月)的患者。我们分别使用广义线性和 Cox 比例风险回归模型来确定成本和结局的决定因素。
与月均费用变化相关的关键变量包括:二线治疗方案;治疗开始前 4 个月至治疗后 4 个月期间开始接受 ART 治疗;最近或当前 CD4 计数<50 个细胞/微升或 50-199 个细胞/微升;每月药物补充数据显示 ART 依从性<75%;当前或近期病毒载量>100000 拷贝/ml。就死亡的可能性而言,关键变量是:基线 CD4 计数<50 个细胞/微升(尤其是治疗的前 4 个月);当前 CD4 计数<50 个细胞/微升和 50-199 个细胞/微升(尤其是治疗后期);二线治疗方案。依从性差和病毒载量未被抑制也与死亡可能性增加相关。
尽管扩大 ART 规模所需资源的建模存在许多未知因素,但我们的分析已经提出了一些可以用来改进 ART 建模现状的关键变量。虽然这些变量相关的影响幅度在其他环境中可能有所不同,但影响成本和生存的变量可能具有普遍性。这对于那些关注评估扩大 ART 获得机会的长期成本和可持续性的人具有直接意义。