Blasco Antonio Javier, Arribas José Ramón, Boix Vicente, Clotet Bonaventura, Domingo Pere, González-García Juan, Knobel Hernando, López Juan Carlos, Llibre Josep M, Lozano Fernando, Miró José M, Podzamczer Daniel, Santamaría Juan Miguel, Tuset Montserrat, Zamora Laura, Lázaro Pablo, Gatell Josep M
Técnicas Avanzadas de Investigación en Servicios de Salud (TAISS), Madrid, España.
Enferm Infecc Microbiol Clin. 2012 Jun;30(6):283-93. doi: 10.1016/j.eimc.2012.02.016. Epub 2012 Apr 22.
The GESIDA and National AIDS Plan panel of experts propose «preferred regimens» of antiretroviral treatment (ART) as initial therapy in HIV infected patients for 2012. The objective of this study is to evaluate the costs and the efficiency of initiating treatment with these «preferred regimens».
Economic assessment of costs and efficiency (cost/efficacy) using decision tree analysis model. Efficacy was defined as the probability of having a viral load <50 copies/ml at week 48, in an intention-to-treat analysis. Cost of initiating treatment with an ART regime was defined as the costs of ART and all its consequences (adverse effects, changes of ART regime, and drug resistance analyses) during the first 48 weeks. The perspective of the analysis is that of the National Health System, considering only differential direct costs: ART (official prices), management of adverse effects, studies of resistance and determination of HLA B 5701. The setting is Spain and the costs are those of 2012. A sensitivity deterministic analysis was conducted, building three scenarios for each regime: baseline, most favourable, and most unfavourable cases.
In the baseline case scenario, the cost of initiating treatment ranges from 6,895 euros for TDF/FTC+NVP to 12,067 euros for TDF/FTC+RAL. The efficacy ranges between 0.66 for ABC/3TC+LPV/r and 0.87 for TDF/FTC+RAL. Efficiency, in terms of cost/efficacy, varies between 9,387 and 13,823 euros per responder at 48 weeks, for TDF/FTC/EFV and TDF/FTC+RAL, respectively. In the most unfavourable scenario, the most efficient regime is TDF/FTC+NVP (9,742 per responder).
Considering the official prices of ART, the most efficient regimens are TDF/FTC/EFV (baseline case and most favourable scenarios), and TDF/FTC+NVP (most unfavourable scenario).
西班牙艾滋病研究与治疗协作组(GESIDA)和国家艾滋病规划专家小组提出了2012年针对HIV感染患者抗逆转录病毒治疗(ART)的“首选方案”作为初始治疗方案。本研究的目的是评估采用这些“首选方案”开始治疗的成本和效果。
使用决策树分析模型对成本和效果(成本/疗效)进行经济评估。在意向性分析中,疗效定义为第48周时病毒载量<50拷贝/ml的概率。采用ART方案开始治疗的成本定义为前48周内ART及其所有后果(不良反应、ART方案变更和耐药性分析)的成本。分析的视角是国家卫生系统,仅考虑直接差异成本:ART(官方价格)、不良反应管理、耐药性研究以及HLA B 5701检测。研究背景为西班牙,成本为2012年的成本。进行了敏感性确定性分析,针对每个方案构建了三种情景:基线情景、最有利情景和最不利情景。
在基线情景下,开始治疗的成本从替诺福韦酯/恩曲他滨+奈韦拉平(TDF/FTC+NVP)的6895欧元到替诺福韦酯/恩曲他滨+拉替拉韦(TDF/FTC+RAL)的12067欧元不等。疗效在阿巴卡韦/拉米夫定+洛匹那韦/利托那韦(ABC/3TC+LPV/r)为0.66和替诺福韦酯/恩曲他滨+拉替拉韦为0.87之间。就成本/疗效而言,替诺福韦酯/恩曲他滨/依非韦伦(TDF/FTC/EFV)和替诺福韦酯/恩曲他滨+拉替拉韦在第48周时每位有反应者的效率分别在9387至13823欧元之间。在最不利情景下,最有效的方案是替诺福韦酯/恩曲他滨+奈韦拉平(每位有反应者9742欧元)。
考虑到ART的官方价格,最有效的方案是替诺福韦酯/恩曲他滨/依非韦伦(基线情景和最有利情景)以及替诺福韦酯/恩曲他滨+奈韦拉平(最不利情景)。