Cost-Utility Model of Nirmatrelvir/Ritonavir in Brazil: Analysis of a Vaccinated Population

IF 1.4 Q3 HEALTH CARE SCIENCES & SERVICES
Ricardo R.A. Fernandes PhD , Bruno M. Barros MSc , Milene R. da Costa PhD , Carlos A.S. Magliano PhD , Bernardo R. Tura PhD , Quenia Cristina D. Morais MSc , Marisa Santos PhD
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Abstract

Objectives

The aim of this study is to conduct a cost-utility analysis of the use of the antiviral nirmatrelvir/ritonavir, applied to a vaccinated Brazilian population against COVID-19, from the perspective of the Brazilian Public Health System (SUS).

Methods

A microsimulation model was created with individual-level data and daily cycles, with a 1-year time horizon, to compare the current scenario of standard care with a scenario in which nirmatrelvir/ritonavir is offered to the population. Adults of any age group that received ≥2 doses of the COVID-19 vaccine formed the investigated population. Direct medical costs of the outpatients and inpatients admitted to the ward or intensive care unit were included. The effectiveness of the model was measured in quality-adjusted life-years (QALYs).

Results

In all simulations, the use of nirmatrelvir/ritonavir resulted in incremental costs per patient of US dollar (USD)245.86 and incremental effectiveness of 0.009 QALY, over a year. The incremental cost-utility ratio was USD27 220.70/QALY. The relative risk of the vaccinated population was the factor that affected the outcome most, according to the univariate sensitivity analysis. The probabilistic sensitivity analysis resulted in 100% of the simulations being more costly and effective, but that only 4% of them were below the established cost-effectiveness threshold of USD24 000.00/QALY. In the scenario considering only the population over 60 years old and immunosuppressed (of any age), the incremental cost-utility ratio was USD7589.37/QALY.

Conclusions

The use of nirmatrelvir/ritonavir in the treatment of COVID-19 in a vaccinated population was cost-effective only for immunosuppressed individuals and people over 60 years of age.

巴西尼马特韦/利托那韦的成本效用模型:对接种人群的分析。
目的:本研究的目的是从巴西公共卫生系统(SUS)的角度,对巴西接种COVID-19疫苗的人群使用抗病毒药物nirmatrelvir/ritonavir进行成本效用分析。方法:建立了一个微观模拟模型,其中包含个人层面的数据和1年时间范围内的每日周期,以比较目前标准治疗方案与向人群提供尼马特利韦/利托那韦的方案。接受≥2剂COVID-19疫苗的任何年龄组的成年人构成调查人群。门诊病人和住院病人入住病房或重症监护病房的直接医疗费用也包括在内。该模型的有效性以质量调整生命年(QALYs)来衡量。结果:在所有模拟中,使用尼马特利韦/利托那韦导致每名患者一年的增量成本为245.86美元,增量有效性为0.009 QALY。增量成本效用比为27220.70美元/QALY。根据单变量敏感性分析,接种人群的相对风险是影响结果最大的因素。概率敏感性分析结果表明,100%的模拟成本和效果更高,但只有4%的模拟低于既定的成本-效果阈值usd24000.00 /QALY。在仅考虑60岁以上人群和免疫抑制人群(任何年龄)的情况下,增量成本-效用比为7589.37美元/QALY。结论:在接种疫苗的人群中,使用尼马特利韦/利托那韦治疗COVID-19仅对免疫抑制个体和60岁以上的人群具有成本效益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Value in health regional issues
Value in health regional issues Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
2.60
自引率
5.00%
发文量
127
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