依杜硫酶长期治疗亨特综合征的成本-效果分析

IF 1.4 Q3 HEALTH CARE SCIENCES & SERVICES
Khairu Hazwan Mustaffa MSc , Asrul Akmal Shafie PhD , Lock-Hock Ngu MBBS , Rowani Mohd-Rawi MBBS
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引用次数: 0

摘要

目的亨特综合征是代价最高的终生遗传性疾病之一,与巨大的疾病负担和对卫生系统、家庭和社会的重大影响有关。我们从社会角度出发,使用R.简化的建模策略,估计了idursulase长期酶替代治疗与标准护理的成本-效果。方法建立了一个从头开始的四状态分区生存模型,以比较R.运行的两种护理模型的终生成本和结果。疾病进展基于相关Kaplan-Meier数据的独立生存模型。医疗保健和自付费用来自当地环境。使用EQ5D5L和与模型中状态匹配的健康状态片段的时间权衡评估来测量生活质量。进行了概率和确定性敏感性分析,以检验模型结果的不确定性。结果终生质量调整生命年增量为4.1年(95% CI, 2.37 ~ 5.68)。增量成本估计为950万美元(95% CI, 900万- 1000万),其中主要包括药品成本(99%)。每个质量调整生命年的增量成本估计约为240万美元(95% CI, 170万- 380万)。敏感性分析显示,增加成本-效果比的关键驱动因素是进展前状态的生活质量和差异贴现方法,以及idursulase酶替代治疗的获取成本。结论所有病例的增量成本-效果比均超过任何常规使用的成本-效果阈值。在目前的价格下,该疗法的资助决定与作为指导马来西亚医疗保健优先次序基础的成本效益评估之间存在显著差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cost-Effectiveness Analysis of Idursulfase for the Long-Term Treatment of Hunter Syndrome Using a Partitioned-Survival Model Approach in R

Objectives

Hunter syndrome is among the costliest life-long genetic conditions associated with a substantial burden-of-illness and a significant impact on the health systems, families, and society. We estimated the cost-effectiveness of long-term enzyme replacement therapy with idursulfase versus the standard of care from a societal perspective using a streamlined modeling strategy in R.

Methods

A de novo 4-state partitioned survival model was developed to compare lifetime cost and outcomes of 2 care models operationalized in R. The disease progression was based on independent survival modeling of relevant Kaplan-Meier data. The healthcare and out-of-pocket costs were drawn from the local setting. The quality of life was measured using the EQ5D5L and the time trade-off valuation of health-state vignettes that match the states in the model. Probabilistic and deterministic sensitivity analyses were conducted to test the uncertainty around the model results.

Results

The lifetime incremental quality-adjusted life years were 4.1 years (95% CI, 2.37-5.68). Incremental costs were estimated to be $9.5 million (95% CI, 9.0 million-10.0 million), which primarily consists of drug costs (99%). The incremental costs per quality-adjusted life year were estimated to be approximately $2.4 million (95% CI, 1.7 million-3.8 million). Sensitivity analyses showed that the key drivers of incremental cost-effectiveness ratio were quality of life in the preprogression state and differential discounting approach, besides the acquisition cost of enzyme replacement therapy of idursulfase.

Conclusions

The incremental cost-effectiveness ratios were beyond any conventionally used cost-effectiveness threshold in all cases. At the current price, there is a significant discrepancy between the therapy’s funding decision and the cost-effectiveness assessment as a basis for guiding healthcare prioritization in Malaysia.
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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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