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中国法布里病患者酶替代疗法治疗的成本效益分析:马尔可夫模型

Cost-effectiveness analysis of enzyme replacement therapy for the treatment of Chinese patients with fabry disease: a Markov model.

作者信息

Huang Yueyang, Yuan Hongmei, Huang Zhe

机构信息

School of Business Administration, Shenyang Pharmaceutical University, Shenyang, China.

出版信息

Front Pharmacol. 2025 Mar 11;16:1546018. doi: 10.3389/fphar.2025.1546018. eCollection 2025.

Abstract

BACKGROUND

Fabry disease (FD) is an X-chromosome-linked genetic disorder. Currently, the main treatments for FD include disease-nonspecific and disease-specific treatments. Nonspecific treatment involves symptomatic management of organ involvement. On the other hand, disease-specific treatment is to regulate the activity of the corresponding enzymes, which is targeted. Among them, enzyme replacement therapy (ERT) is a classical therapy. Several studies have demonstrated the significant ameliorative effect of agalactosidase-α (ALTA-a) on cardiac and renal function in patients with FD. Despite the excellent clinical performance, there are limited pharmacoeconomic studies on ERT for FD worldwide.

OBJECTIVE

The aim of this study was to analyze the cost-effectiveness of ERT for FD in China from the perspective of the healthcare system.

METHODS

We constructed a five-state Markov model based on the disease characteristics of FD. The modeling period was 1 month. The time horizon was 3 years. The willingness-to-pay threshold was chosen as 1-3 times the gross national product (GDP) . The incremental cost-effectiveness ratio (ICER) was calculated from the base case analysis, and one-way sensitivity analysis and probabilistic sensitivity analysis were performed.

RESULTS

The ICER value is ¥148071.95/QALY, which is between 1-3 times GDP . The sensitivity analysis showed that the cost of ALTA-a had a significant effect on ICER and proved the stability of the results.

CONCLUSION

ERT therapy is a cost-effective program compared to "No ERT" therapy.

摘要

背景

法布里病(FD)是一种X染色体连锁的遗传性疾病。目前,FD的主要治疗方法包括非特异性治疗和特异性治疗。非特异性治疗涉及对器官受累情况进行对症处理。另一方面,特异性治疗是调节相应酶的活性,具有针对性。其中,酶替代疗法(ERT)是一种经典疗法。多项研究已证实α-半乳糖苷酶(ALTA-a)对FD患者的心脏和肾功能有显著改善作用。尽管临床疗效出色,但全球范围内针对FD的ERT药物经济学研究有限。

目的

本研究旨在从医疗保健系统的角度分析中国FD患者ERT治疗的成本效益。

方法

我们基于FD的疾病特征构建了一个五状态马尔可夫模型。建模周期为1个月。时间跨度为3年。支付意愿阈值设定为国民生产总值(GDP)的1至3倍。通过基础病例分析计算增量成本效益比(ICER),并进行单向敏感性分析和概率敏感性分析。

结果

ICER值为148071.95元/QALY,处于GDP的1至3倍之间。敏感性分析表明,ALTA-a的成本对ICER有显著影响,并证明了结果的稳定性。

结论

与“不进行ERT”治疗相比,ERT治疗是一个具有成本效益的方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f43a/11932859/00c661c32dab/fphar-16-1546018-g001.jpg

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